-
1
-
-
44649110874
-
-
Wiley-VCH: Weinheim, Germany
-
Breitmaier, E. Terpenes: Flavors, Fragrances, Pharmaca, Pheromones; Wiley-VCH: Weinheim, Germany, 2006.
-
(2006)
Terpenes: Flavors, Fragrances, Pharmaca, Pheromones
-
-
Breitmaier, E.1
-
2
-
-
66349139329
-
New microbial fuels: A biotech perspective
-
Rude, M. A.; Schirmer, A. New microbial fuels: a biotech perspective Curr. Opin. Microbiol. 2009, 12, 274-281 10.1016/j.mib.2009.04.004
-
(2009)
Curr. Opin. Microbiol.
, vol.12
, pp. 274-281
-
-
Rude, M.A.1
Schirmer, A.2
-
3
-
-
84871880840
-
Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin
-
Wilbon, P. A.; Chu, F.; Tang, C. Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin Macromol. Rapid Commun. 2013, 34, 8-37 10.1002/marc.201200513
-
(2013)
Macromol. Rapid Commun.
, vol.34
, pp. 8-37
-
-
Wilbon, P.A.1
Chu, F.2
Tang, C.3
-
4
-
-
0742318457
-
The chiral pool as a source of enantioselective catalysts and auxiliaries
-
Blaser, H.-U. The chiral pool as a source of enantioselective catalysts and auxiliaries Chem. Rev. 1992, 92, 935-952 10.1021/cr00013a009
-
(1992)
Chem. Rev.
, vol.92
, pp. 935-952
-
-
Blaser, H.-U.1
-
5
-
-
85130515720
-
-
2 nd ed. CRC Press, Taylor & Francis: Boca Raton, FL
-
Handbook of Chiral Chemicals, 2 nd ed.; Ager, D., Ed.; CRC Press, Taylor & Francis: Boca Raton, FL, 2005.
-
(2005)
Handbook of Chiral Chemicals
-
-
Ager, D.1
-
7
-
-
0003023759
-
Monosaccharides as Chiral Pools for the Synthesis of Complex Natural Compounds
-
2 nd ed. Fraser-Reid, B. O. Tatsuta, K. Thiem, J. Springer-Verlag: Berlin, Vol. Chapter 4.4
-
Nakata, M. Monosaccharides as Chiral Pools for the Synthesis of Complex Natural Compounds. In Glycoscience, 2 nd ed.; Fraser-Reid, B. O.; Tatsuta, K.; Thiem, J., Eds.; Springer-Verlag: Berlin, 2008; Vol. 2, Chapter 4.4, pp 957-994.
-
(2008)
Glycoscience
, vol.2
, pp. 957-994
-
-
Nakata, M.1
-
8
-
-
84902425756
-
Chiral Pool Synthesis: Chiral Pool Syntheses Starting from Carbohydrates
-
Elsevier: Vol
-
Chida, N.; Sato, T. Chiral Pool Synthesis: Chiral Pool Syntheses Starting from Carbohydrates. In Comprehensive Chirality; Elsevier: 2012; Vol. 2, pp 207-239.
-
(2012)
Comprehensive Chirality
, vol.2
, pp. 207-239
-
-
Chida, N.1
Sato, T.2
-
9
-
-
84979031590
-
Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis
-
Paek, S.-M.; Jeong, M.; Jo, J.; Heo, Y. M.; Han, Y. T.; Yun, H. Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis Molecules 2016, 21, 951 10.3390/molecules21070951
-
(2016)
Molecules
, vol.21
, pp. 951
-
-
Paek, S.-M.1
Jeong, M.2
Jo, J.3
Heo, Y.M.4
Han, Y.T.5
Yun, H.6
-
11
-
-
77957043890
-
The Use of Cyclic Monoterpenoids as Enantiopure Starting Materials in Natural Product Synthesis
-
Money, T.; Wong, M. K. C. The Use of Cyclic Monoterpenoids as Enantiopure Starting Materials in Natural Product Synthesis Stud. Nat. Prod. Chem. 1995, 16, 123-288 10.1016/S1572-5995(06)80054-2
-
(1995)
Stud. Nat. Prod. Chem.
, vol.16
, pp. 123-288
-
-
Money, T.1
Wong, M.K.C.2
-
13
-
-
0000181440
-
The isoprene rule and the biogenesis of terpenic compounds
-
Ruzicka, L. The isoprene rule and the biogenesis of terpenic compounds Experientia 1953, 9, 357-367 10.1007/BF02167631
-
(1953)
Experientia
, vol.9
, pp. 357-367
-
-
Ruzicka, L.1
-
14
-
-
30144439471
-
Revisited after 50 Years: The 'Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes,'
-
Eschenmoser, A.; Arigoni, D. Revisited after 50 Years: The 'Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes,' Helv. Chim. Acta 2005, 88, 3011-3050 10.1002/hlca.200590245
-
(2005)
Helv. Chim. Acta
, vol.88
, pp. 3011-3050
-
-
Eschenmoser, A.1
Arigoni, D.2
-
15
-
-
84962367258
-
Natural Products as Sources of New Drugs from 1981 to 2014
-
Newman, D. J.; Cragg, G. M. Natural Products as Sources of New Drugs from 1981 to 2014 J. Nat. Prod. 2016, 79, 629-661 10.1021/acs.jnatprod.5b01055
-
(2016)
J. Nat. Prod.
, vol.79
, pp. 629-661
-
-
Newman, D.J.1
Cragg, G.M.2
-
16
-
-
0000305326
-
Beyond Nature's Chiral Pool: Enantioselective Catalysis in Industry
-
Nugent, W. A.; RajanBabu, T. V.; Burk, M. J. Beyond Nature's Chiral Pool: Enantioselective Catalysis in Industry Science 1993, 259, 479-483 10.1126/science.259.5094.479
-
(1993)
Science
, vol.259
, pp. 479-483
-
-
Nugent, W.A.1
RajanBabu, T.V.2
Burk, M.J.3
-
17
-
-
34250697565
-
Modern synthetic efforts toward biologically active terpenes
-
Maimone, T. J.; Baran, P. S. Modern synthetic efforts toward biologically active terpenes Nat. Chem. Biol. 2007, 3, 396-407 10.1038/nchembio.2007.1
-
(2007)
Nat. Chem. Biol.
, vol.3
, pp. 396-407
-
-
Maimone, T.J.1
Baran, P.S.2
-
18
-
-
84905482376
-
Synthesis of medicinally relevant terpenes: Reducing the cost and time of drug discovery
-
Jansen, D. J.; Shenvi, R. A. Synthesis of medicinally relevant terpenes: reducing the cost and time of drug discovery Future Med. Chem. 2014, 6, 1127-1148 10.4155/fmc.14.71
-
(2014)
Future Med. Chem.
, vol.6
, pp. 1127-1148
-
-
Jansen, D.J.1
Shenvi, R.A.2
-
19
-
-
84982141478
-
Recent advances in terpenoid synthesis from China
-
Qiao, T.; Liang, G. Recent advances in terpenoid synthesis from China Sci. China: Chem. 2016, 59, 1142-1174 10.1007/s11426-016-0076-6
-
(2016)
Sci. China: Chem.
, vol.59
, pp. 1142-1174
-
-
Qiao, T.1
Liang, G.2
-
20
-
-
84941134584
-
Convergent Strategies in Total Syntheses of Complex Terpenoids
-
Urabe, D.; Asaba, T.; Inoue, M. Convergent Strategies in Total Syntheses of Complex Terpenoids Chem. Rev. 2015, 115, 9207-9231 10.1021/cr500716f
-
(2015)
Chem. Rev.
, vol.115
, pp. 9207-9231
-
-
Urabe, D.1
Asaba, T.2
Inoue, M.3
-
21
-
-
84902414927
-
-
Carreira, E. M. Yamamoto, H. Elsevier Ltd
-
Gaich, T.; Mulzer, J. In Comprehensive Chirality; Carreira, E. M.; Yamamoto, H., Eds.; Elsevier Ltd.: 2012; Vol. 2, pp 163-206.
-
(2012)
Comprehensive Chirality
, vol.2
, pp. 163-206
-
-
Gaich, T.1
Mulzer, J.2
-
22
-
-
36349031083
-
Steroids: Partial synthesis in medicinal chemistry
-
Hanson, J. R. Steroids: partial synthesis in medicinal chemistry Nat. Prod. Rep. 2007, 24, 1342-1349 10.1039/b705948p
-
(2007)
Nat. Prod. Rep.
, vol.24
, pp. 1342-1349
-
-
Hanson, J.R.1
-
24
-
-
85030089997
-
-
Lowest price (USD) in bulk quantities as of October 2016
-
Lowest price (USD) in bulk quantities as of October 2016.
-
-
-
-
25
-
-
34249857059
-
Citronellal as a key compound in organic synthesis
-
Lenardao, E. J.; Botteselle, G. V.; de Azambuja, F.; Perin, G.; Jacob, R. G. Citronellal as a key compound in organic synthesis Tetrahedron 2007, 63, 6671-6712 10.1016/j.tet.2007.03.159
-
(2007)
Tetrahedron
, vol.63
, pp. 6671-6712
-
-
Lenardao, E.J.1
Botteselle, G.V.2
De Azambuja, F.3
Perin, G.4
Jacob, R.G.5
-
26
-
-
0003445429
-
-
Jacobsen, E. N. Pfaltz, A. Yamamoto, H. Springer: New York, Vol. Chapter 41.4
-
Akutagawa, S. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: New York, 1999; Vol. 3, Chapter 41.4.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.3
-
-
Akutagawa, S.1
-
27
-
-
40949111966
-
An Efficient Procedure for the 1,3-Transposition of Allylic Alcohols Based on Lithium Naphthalenide Induced Reductive Elimination of Epoxy Mesylates
-
Wu, Y.-K.; Liu, H.-J.; Zhu, J.-L. An Efficient Procedure for the 1,3-Transposition of Allylic Alcohols Based on Lithium Naphthalenide Induced Reductive Elimination of Epoxy Mesylates Synlett 2008, 621-623 10.1055/s-2008-1032092
-
(2008)
Synlett
, pp. 621-623
-
-
Wu, Y.-K.1
Liu, H.-J.2
Zhu, J.-L.3
-
28
-
-
84875461275
-
Bioactive Natural Products from Enantiomeric Carvones
-
Atta-ur-Rahman, Elsevier: Vol. Chapter 7
-
Macaev, F. Z. Bioactive Natural Products from Enantiomeric Carvones. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: 2013; Vol. 39, Chapter 7.
-
(2013)
Studies in Natural Products Chemistry
, vol.39
-
-
Macaev, F.Z.1
-
29
-
-
0022079803
-
Camphor: A chiral starting material in natural product synthesis
-
Money, T. Camphor: a chiral starting material in natural product synthesis Nat. Prod. Rep. 1985, 2, 253-289 10.1039/np9850200253
-
(1985)
Nat. Prod. Rep.
, vol.2
, pp. 253-289
-
-
Money, T.1
-
30
-
-
0000108328
-
Preparation, stereochemistry, and nuclear magnetic resonance spectroscopy of 4-hydroxy(acetoxy)bicyclo[5.1.0]octanes. Synthesis of (-)- and (±)-8,8-dimethylbicyclo[5.1.0]oct-2-en-4-one
-
Taylor, M. D.; Minaskanian, G.; Winzenberg, K. N.; Santone, P.; Smith, A. B., III. Preparation, stereochemistry, and nuclear magnetic resonance spectroscopy of 4-hydroxy(acetoxy)bicyclo[5.1.0]octanes. Synthesis of (-)- and (±)-8,8-dimethylbicyclo[5.1.0]oct-2-en-4-one J. Org. Chem. 1982, 47, 3960-3964 10.1021/jo00141a029
-
(1982)
J. Org. Chem.
, vol.47
, pp. 3960-3964
-
-
Taylor, M.D.1
Minaskanian, G.2
Winzenberg, K.N.3
Santone, P.4
Smith, B.S.A.5
-
31
-
-
85027954450
-
Trends in the Synthesis and Functionalization of Guaianolides
-
Santana, A.; Molinillo, J. M. G.; Macías, F. A. Trends in the Synthesis and Functionalization of Guaianolides Eur. J. Org. Chem. 2015, 2093-2110 10.1002/ejoc.201403244
-
(2015)
Eur. J. Org. Chem.
, pp. 2093-2110
-
-
Santana, A.1
Molinillo, J.M.G.2
Macías, F.A.3
-
32
-
-
84945115676
-
An eight-step synthesis of epicolactone reveals its biosynthetic origin
-
Ellerbrock, P.; Armanino, N.; Ilg, M. K.; Webster, R.; Trauner, D. An eight-step synthesis of epicolactone reveals its biosynthetic origin Nat. Chem. 2015, 7, 879-882 10.1038/nchem.2336
-
(2015)
Nat. Chem.
, vol.7
, pp. 879-882
-
-
Ellerbrock, P.1
Armanino, N.2
Ilg, M.K.3
Webster, R.4
Trauner, D.5
-
33
-
-
0018601535
-
Total synthesis of picrotoxinin
-
Corey, E. J.; Pearce, H. L. Total synthesis of picrotoxinin J. Am. Chem. Soc. 1979, 101, 5841-5843 10.1021/ja00513a071
-
(1979)
J. Am. Chem. Soc.
, vol.101
, pp. 5841-5843
-
-
Corey, E.J.1
Pearce, H.L.2
-
34
-
-
0020577131
-
Total synthesis of qinghaosu
-
Schmid, G.; Hofheinz, W. Total synthesis of qinghaosu J. Am. Chem. Soc. 1983, 105, 624-625 10.1021/ja00341a054
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 624-625
-
-
Schmid, G.1
Hofheinz, W.2
-
36
-
-
0031470265
-
Total Synthesis of Eleutherobin
-
Nicolaou, K. C.; van Delft, F.; Ohshima, T.; Vourloumis, D.; Xu, J.; Hosokawa, S.; Pfefferkorn, J.; Kim, S.; Li, T. Total Synthesis of Eleutherobin Angew. Chem., Int. Ed. Engl. 1997, 36, 2520-2524 10.1002/anie.199725201
-
(1997)
Angew. Chem., Int. Ed. Engl.
, vol.36
, pp. 2520-2524
-
-
Nicolaou, K.C.1
Van Delft, F.2
Ohshima, T.3
Vourloumis, D.4
Xu, J.5
Hosokawa, S.6
Pfefferkorn, J.7
Kim, S.8
Li, T.9
-
37
-
-
0031882649
-
Total Synthesis of Eleutherobin
-
Chen, X.-T.; Gutteridge, C. E.; Bhattacharya, S. K.; Zhou, B.; Pettus, T. R.; Hascall, T.; Danishefsky, S. J. Total Synthesis of Eleutherobin Angew. Chem., Int. Ed. 1998, 37, 185-187 10.1002/(SICI)1521-3773(19980202)37:1/2<185::AID-ANIE185>3.0.CO;2-L
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 185-187
-
-
Chen, X.-T.1
Gutteridge, C.E.2
Bhattacharya, S.K.3
Zhou, B.4
Pettus, T.R.5
Hascall, T.6
Danishefsky, S.J.7
-
38
-
-
33845376672
-
Macroexpansion methodology. 3. Eight-step synthesis of (-)-(3Z)-cembrene A
-
Wender, P. A.; Holt, D. A. Macroexpansion methodology. 3. Eight-step synthesis of (-)-(3Z)-cembrene A J. Am. Chem. Soc. 1985, 107, 7771-7772 10.1021/ja00311a096
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 7771-7772
-
-
Wender, P.A.1
Holt, D.A.2
-
39
-
-
0000011222
-
Total synthesis of (+)-jatropholone A and B
-
Smith, A. B., III.; Liverton, N. J.; Hrib, N. J.; Sivaramakrishnan, H.; Winzenberg, K. N. Total synthesis of (+)-jatropholone A and B J. Org. Chem. 1985, 50, 3239-3241 10.1021/jo00217a054
-
(1985)
J. Org. Chem.
, vol.50
, pp. 3239-3241
-
-
Smith, B.S.A.1
Liverton, N.J.2
Hrib, N.J.3
Sivaramakrishnan, H.4
Winzenberg, K.N.5
-
40
-
-
0000431466
-
Total synthesis of (+)-ophiobolin C
-
Rowley, M.; Tsukamoto, M.; Kishi, Y. Total synthesis of (+)-ophiobolin C J. Am. Chem. Soc. 1989, 111, 2735-2731 10.1021/ja00189a069
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 2731-2735
-
-
Rowley, M.1
Tsukamoto, M.2
Kishi, Y.3
-
41
-
-
34347335758
-
Strategies to Bypass the Taxol Problem. Enantioselective cascade catalysis, a New Approach for the Efficient Construction of Molecular Complexity
-
Walji, A. B.; Macmillan, D. W. Strategies to Bypass the Taxol Problem. Enantioselective cascade catalysis, a New Approach for the Efficient Construction of Molecular Complexity Synlett 2007, 1477-1489 10.1055/s-2007-980382
-
(2007)
Synlett
, pp. 1477-1489
-
-
Walji, A.B.1
MacMillan, D.W.2
-
42
-
-
77954842094
-
Two-Phase Terpene Total Synthesis: Historical Perspective and Application to the Taxol® Problem
-
Ishihara, Y.; Baran, P. S. Two-Phase Terpene Total Synthesis: Historical Perspective and Application to the Taxol® Problem Synlett 2010, 1733-1745 10.1055/s-0030-1258123
-
(2010)
Synlett
, pp. 1733-1745
-
-
Ishihara, Y.1
Baran, P.S.2
-
43
-
-
0030936927
-
The Pinene Path to Taxanes. 6. A Concise Stereocontrolled Synthesis of Taxol
-
Wender, P. A.; Badham, N. F.; Conway, S. P.; Floreancig, P. E.; Glass, T. E.; Houze, J. B.; Krauss, N. E.; Lee, D.; Marquess, D. G.; McGrane, P. L. et al. The Pinene Path to Taxanes. 6. A Concise Stereocontrolled Synthesis of Taxol J. Am. Chem. Soc. 1997, 119, 2757-2758 10.1021/ja963539z
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 2757-2758
-
-
Wender, P.A.1
Badham, N.F.2
Conway, S.P.3
Floreancig, P.E.4
Glass, T.E.5
Houze, J.B.6
Krauss, N.E.7
Lee, D.8
Marquess, D.G.9
McGrane, P.L.10
-
44
-
-
0028353983
-
First total synthesis of taxol. 2. Completion of the C and D rings
-
Holton, R. A.; Kim, H. B.; Somoza, C.; Liang, F.; Biediger, R. J.; Boatman, P. D.; Shindo, M.; Smith, C. C.; Kim, S. First total synthesis of taxol. 2. Completion of the C and D rings J. Am. Chem. Soc. 1994, 116, 1599-1600 10.1021/ja00083a067
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 1599-1600
-
-
Holton, R.A.1
Kim, H.B.2
Somoza, C.3
Liang, F.4
Biediger, R.J.5
Boatman, P.D.6
Shindo, M.7
Smith, C.C.8
Kim, S.9
-
45
-
-
70349769724
-
Redox Economy in Organic Synthesis
-
Burns, N. Z.; Baran, P. S.; Hoffmann, R. W. Redox Economy in Organic Synthesis Angew. Chem., Int. Ed. 2009, 48, 2854-2867 10.1002/anie.200806086
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 2854-2867
-
-
Burns, N.Z.1
Baran, P.S.2
Hoffmann, R.W.3
-
46
-
-
38949138457
-
Function-Oriented Synthesis, Step Economy, and Drug Design
-
Wender, P. A.; Verma, V. A.; Paxton, T. J.; Pillow, T. H. Function-Oriented Synthesis, Step Economy, and Drug Design Acc. Chem. Res. 2008, 41, 40-49 10.1021/ar700155p
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 40-49
-
-
Wender, P.A.1
Verma, V.A.2
Paxton, T.J.3
Pillow, T.H.4
-
47
-
-
33751317736
-
Protecting-Group-Free Synthesis
-
Hoffmann, R. W. Protecting-Group-Free Synthesis Synthesis 2006, 21) 3531-3541 10.1055/s-2006-950311
-
(2006)
Synthesis
, Issue.21
, pp. 3531-3541
-
-
Hoffmann, R.W.1
-
48
-
-
67650984682
-
Protecting-group-free synthesis as an opportunity for invention
-
Young, I. S.; Baran, P. S. Protecting-group-free synthesis as an opportunity for invention Nat. Chem. 2009, 1, 193-205 10.1038/nchem.216
-
(2009)
Nat. Chem.
, vol.1
, pp. 193-205
-
-
Young, I.S.1
Baran, P.S.2
-
49
-
-
70350500463
-
The economies of synthesis
-
Newhouse, T.; Baran, P. S.; Hoffmann, R. W. The economies of synthesis Chem. Soc. Rev. 2009, 38, 3010-3021 10.1039/b821200g
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3010-3021
-
-
Newhouse, T.1
Baran, P.S.2
Hoffmann, R.W.3
-
50
-
-
15744379986
-
Total Synthesis of Brasoside and Littoralisone
-
Mangion, I. K.; Macmillan, D. W. C. Total Synthesis of Brasoside and Littoralisone J. Am. Chem. Soc. 2005, 127, 3696-3697 10.1021/ja050064f
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3696-3697
-
-
Mangion, I.K.1
MacMillan, D.W.C.2
-
51
-
-
82255180232
-
Anti-inflammatory and immunomodulatory effects of Paeonia lactiflora Pall., a traditional Chinese herbal medicine
-
He, D.-Y.; Dai, S.-M. Anti-inflammatory and immunomodulatory effects of Paeonia lactiflora Pall., a traditional Chinese herbal medicine Front. Pharmacol. 2011, 2, online 10.3389/fphar.2011.00010
-
(2011)
Front. Pharmacol.
, vol.2
, pp. online
-
-
He, D.-Y.1
Dai, S.-M.2
-
52
-
-
75449094617
-
Chemical constituents and bioactivities of plants from the genus Paeonia
-
Wu, S.-H.; Wu, D.-G.; Chen, Y.-W. Chemical constituents and bioactivities of plants from the genus Paeonia Chem. Biodiversity 2010, 7, 90-104 10.1002/cbdv.200800148
-
(2010)
Chem. Biodiversity
, vol.7
, pp. 90-104
-
-
Wu, S.-H.1
Wu, D.-G.2
Chen, Y.-W.3
-
53
-
-
0027525625
-
Total synthesis of (±)-paeoniflorigenin and paeoniflorin
-
Corey, E. J.; Wu, Y.-J. Total synthesis of (±)-paeoniflorigenin and paeoniflorin J. Am. Chem. Soc. 1993, 115, 8871-8872 10.1021/ja00072a063
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 8871-8872
-
-
Corey, E.J.1
Wu, Y.-J.2
-
54
-
-
0028285827
-
Total Synthesis of (-)-Paeoniflorin
-
Hatakeyama, S.; Kawamura, M.; Takano, S. Total Synthesis of (-)-Paeoniflorin J. Am. Chem. Soc. 1994, 116, 4081-4082 10.1021/ja00088a055
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4081-4082
-
-
Hatakeyama, S.1
Kawamura, M.2
Takano, S.3
-
55
-
-
0028870275
-
Total syntheses of (+)-paeonilactone B and (-)-paeonisuffrone
-
Hatakeyama, S.; Kawamura, M.; Mukugi, Y.; Irie, H. Total syntheses of (+)-paeonilactone B and (-)-paeonisuffrone Tetrahedron Lett. 1995, 36, 267-268 10.1016/0040-4039(94)02189-I
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 267-268
-
-
Hatakeyama, S.1
Kawamura, M.2
Mukugi, Y.3
Irie, H.4
-
56
-
-
64349087045
-
Ti(III)-Promoted Radical Cyclization of Epoxy Enones. Total Synthesis of (+)-Paeonisuffrone
-
Martín-Rodríguez, M.; Galán-Fernández, R.; Marcos-Escribano, A.; Bermejo, F. A. Ti(III)-Promoted Radical Cyclization of Epoxy Enones. Total Synthesis of (+)-Paeonisuffrone J. Org. Chem. 2009, 74, 1798-1801 10.1021/jo8026033
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1798-1801
-
-
Martín-Rodríguez, M.1
Galán-Fernández, R.2
Marcos-Escribano, A.3
Bermejo, F.A.4
-
57
-
-
33746805390
-
Ti(III)-promoted cyclizations. Application to the synthesis of (E)-endo-bergamoten-12-oic acids. Moth oviposition stimulants isolated from Lycopersicon hirsutum
-
Bermejo, F. A.; Mateos, A. F.; Escribano, A. M.; Lago, R. M.; Burón, L. M.; López, M. R.; González, R. R. Ti(III)-promoted cyclizations. Application to the synthesis of (E)-endo-bergamoten-12-oic acids. Moth oviposition stimulants isolated from Lycopersicon hirsutum Tetrahedron 2006, 62, 8933-8942 10.1016/j.tet.2006.07.020
-
(2006)
Tetrahedron
, vol.62
, pp. 8933-8942
-
-
Bermejo, F.A.1
Mateos, A.F.2
Escribano, A.M.3
Lago, R.M.4
Burón, L.M.5
López, M.R.6
González, R.R.7
-
59
-
-
84914690862
-
2TiCl in natural product synthesis
-
2TiCl in natural product synthesis Org. Chem. Front. 2014, 1, 15-33 10.1039/c3qo00024a
-
(2014)
Org. Chem. Front.
, vol.1
, pp. 15-33
-
-
Morcillo, S.P.1
Miguel, D.2
Campana, A.G.3
Álvarez De Cienfuegos, L.4
Justicia, J.5
Cuerva, J.M.6
-
60
-
-
0028925926
-
An antimalarial peroxide from Amomum krervanh Pierre
-
Kamchonwongpaisan, S.; Nilanonta, C.; Tarnchompoo, B.; Thebtaranonth, C.; Thebtaranonth, Y.; Yuthavong, Y.; Kongsaeree, P.; Clardy, J. An antimalarial peroxide from Amomum krervanh Pierre Tetrahedron Lett. 1995, 36, 1821-1824 10.1016/0040-4039(95)00152-3
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 1821-1824
-
-
Kamchonwongpaisan, S.1
Nilanonta, C.2
Tarnchompoo, B.3
Thebtaranonth, C.4
Thebtaranonth, Y.5
Yuthavong, Y.6
Kongsaeree, P.7
Clardy, J.8
-
61
-
-
84857752407
-
Antimalarial peroxides: Advances in drug discovery and design
-
Slack, R. D.; Jacobine, A. M.; Posner, G. H. Antimalarial peroxides: advances in drug discovery and design MedChemComm 2012, 3, 281-297 10.1039/c2md00277a
-
(2012)
MedChemComm
, vol.3
, pp. 281-297
-
-
Slack, R.D.1
Jacobine, A.M.2
Posner, G.H.3
-
62
-
-
3042613588
-
Synthetic peroxides as antimalarials
-
Tang, Y.; Dong, Y.; Vennerstrom, J. L. Synthetic peroxides as antimalarials Med. Res. Rev. 2004, 24, 425-448 10.1002/med.10066
-
(2004)
Med. Res. Rev.
, vol.24
, pp. 425-448
-
-
Tang, Y.1
Dong, Y.2
Vennerstrom, J.L.3
-
63
-
-
67849084837
-
Progress in the development of peroxide-based anti-parasitic agents
-
Muraleedharan, K. M.; Avery, M. A. Progress in the development of peroxide-based anti-parasitic agents Drug Discovery Today 2009, 14, 793-803 10.1016/j.drudis.2009.05.008
-
(2009)
Drug Discovery Today
, vol.14
, pp. 793-803
-
-
Muraleedharan, K.M.1
Avery, M.A.2
-
64
-
-
84898017407
-
Four-Step Synthesis of the Antimalarial Cardamom Peroxide via an Oxygen Stitching Strategy
-
Hu, X.; Maimone, T. J. Four-Step Synthesis of the Antimalarial Cardamom Peroxide via an Oxygen Stitching Strategy J. Am. Chem. Soc. 2014, 136, 5287-5290 10.1021/ja502208z
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5287-5290
-
-
Hu, X.1
Maimone, T.J.2
-
65
-
-
84988001553
-
Using Singlet Oxygen to Synthesize Natural Products and Drugs
-
Ghogare, A. A.; Greer, A. Using Singlet Oxygen to Synthesize Natural Products and Drugs Chem. Rev. 2016, 116, 9994-10034 10.1021/acs.chemrev.5b00726
-
(2016)
Chem. Rev.
, vol.116
, pp. 9994-10034
-
-
Ghogare, A.A.1
Greer, A.2
-
66
-
-
0000038893
-
A new method for preparation of alcohols from olefins with molecular oxygen and phenylsilane by the use of bis(acetylacetonato)cobalt(II)
-
Isayama, S.; Mukaiyama, T. A new method for preparation of alcohols from olefins with molecular oxygen and phenylsilane by the use of bis(acetylacetonato)cobalt(II) Chem. Lett. 1989, 18, 1071-1074 10.1246/cl.1989.1071
-
(1989)
Chem. Lett.
, vol.18
, pp. 1071-1074
-
-
Isayama, S.1
Mukaiyama, T.2
-
67
-
-
0034627347
-
Conversion of α,β-unsaturated ketones into α-hydroxy ketones using an Mn(III) catalyst, phenylsilane and dioxygen: Acceleration of conjugate hydride reduction by dioxygen
-
Magnus, P.; Payne, A. H.; Waring, M. J.; Scott, D. A.; Lynch, V. Conversion of α,β-unsaturated ketones into α-hydroxy ketones using an Mn(III) catalyst, phenylsilane and dioxygen: acceleration of conjugate hydride reduction by dioxygen Tetrahedron Lett. 2000, 41, 9725-9730 10.1016/S0040-4039(00)01727-5
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 9725-9730
-
-
Magnus, P.1
Payne, A.H.2
Waring, M.J.3
Scott, D.A.4
Lynch, V.5
-
69
-
-
85030093257
-
Peroxy Radical Additions
-
Snyder, S. A. Georg Thieme Verlag: Stuttgart, Germany
-
Hu, X.; Maimone, T. J. Peroxy Radical Additions. In Science of Synthesis: Applications of Domino Transformations in Organic Synthesis; Snyder, S. A., Ed.; Georg Thieme Verlag: Stuttgart, Germany, 2016; Vol. 1, pp 157-186.
-
(2016)
Science of Synthesis: Applications of Domino Transformations in Organic Synthesis
, vol.1
, pp. 157-186
-
-
Hu, X.1
Maimone, T.J.2
-
70
-
-
84981724761
-
Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins
-
Crossley, S. W. M.; Martinez, R. M.; Obradors, C.; Shenvi, R. A. Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins Chem. Rev. 2016, 116, 8912-9000 10.1021/acs.chemrev.6b00334
-
(2016)
Chem. Rev.
, vol.116
, pp. 8912-9000
-
-
Crossley, S.W.M.1
Martinez, R.M.2
Obradors, C.3
Shenvi, R.A.4
-
71
-
-
85006848804
-
Bioinspired Total Synthesis of Terpenoids
-
Hugelshofer, C. L.; Magauer, T. Bioinspired Total Synthesis of Terpenoids Org. Biomol. Chem. 2017, 15, 12-16 10.1039/C6OB02488B
-
(2017)
Org. Biomol. Chem.
, vol.15
, pp. 12-16
-
-
Hugelshofer, C.L.1
Magauer, T.2
-
72
-
-
53849102606
-
Total Syntheses of (+)- and (-)-Peribysin e
-
Angeles, A. R.; Waters, S. P.; Danishefsky, S. J. Total Syntheses of (+)- and (-)-Peribysin E J. Am. Chem. Soc. 2008, 130, 13765-13770 10.1021/ja8048207
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13765-13770
-
-
Angeles, A.R.1
Waters, S.P.2
Danishefsky, S.J.3
-
73
-
-
38849153575
-
Enantiospecific Total Synthesis of Lairdinol A
-
Pardeshi, S. G.; Ward, D. E. Enantiospecific Total Synthesis of Lairdinol A J. Org. Chem. 2008, 73, 1071-1076 10.1021/jo7024465
-
(2008)
J. Org. Chem.
, vol.73
, pp. 1071-1076
-
-
Pardeshi, S.G.1
Ward, D.E.2
-
74
-
-
34347226722
-
Total Synthesis and Revised Structure of Biyouyanagin A
-
Nicolaou, K. C.; Sarlah, D.; Shaw, D. M. Total Synthesis and Revised Structure of Biyouyanagin A Angew. Chem., Int. Ed. 2007, 46, 4708-4711 10.1002/anie.200701552
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 4708-4711
-
-
Nicolaou, K.C.1
Sarlah, D.2
Shaw, D.M.3
-
75
-
-
33645688330
-
Platinum- and Gold-Catalyzed Rearrangement Reactions of Propargyl Acetates: Total Syntheses of (-)-α-Cubebene, (-)-Cubebol, Sesquicarene and Related Terpenes
-
Fürstner, A.; Hannen, P. Platinum- and Gold-Catalyzed Rearrangement Reactions of Propargyl Acetates: Total Syntheses of (-)-α-Cubebene, (-)-Cubebol, Sesquicarene and Related Terpenes Chem.-Eur. J. 2006, 12, 3006-3019 10.1002/chem.200501299
-
(2006)
Chem. - Eur. J.
, vol.12
, pp. 3006-3019
-
-
Fürstner, A.1
Hannen, P.2
-
76
-
-
0346093953
-
A route to the thapsigargins from (S)-carvone providing a substrate-controlled total synthesis of trilobolide, nortrilobolide, and thapsivillosin F
-
Oliver, S. F.; Högenauer, K.; Simic, O.; Antonello, A.; Smith, M. D.; Ley, S. V. A route to the thapsigargins from (S)-carvone providing a substrate-controlled total synthesis of trilobolide, nortrilobolide, and thapsivillosin F Angew. Chem., Int. Ed. 2003, 42, 5996-6000 10.1002/anie.200353140
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 5996-6000
-
-
Oliver, S.F.1
Högenauer, K.2
Simic, O.3
Antonello, A.4
Smith, M.D.5
Ley, S.V.6
-
77
-
-
58349113395
-
Diastereoselective total synthesis of 8-epigrosheimin
-
Yang, H.; Qiao, X.; Li, F.; Ma, H.; Xie, L.; Xu, X. Diastereoselective total synthesis of 8-epigrosheimin Tetrahedron Lett. 2009, 50, 1110-1112 10.1016/j.tetlet.2008.12.025
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1110-1112
-
-
Yang, H.1
Qiao, X.2
Li, F.3
Ma, H.4
Xie, L.5
Xu, X.6
-
78
-
-
67649967738
-
Total Synthesis of Valerenic Acid
-
Kopp, S.; Schweizer, W. B.; Altmann, K.-H. Total Synthesis of Valerenic Acid Synlett 2009, 1769-1772 10.1055/s-0029-1217378
-
(2009)
Synlett
, pp. 1769-1772
-
-
Kopp, S.1
Schweizer, W.B.2
Altmann, K.-H.3
-
79
-
-
11844306006
-
Total Synthesis of Absinthin
-
Zhang, W.; Luo, S.; Chen, Q.; Hu, H.; Jia, X.; Zhai, H.; Fang Total Synthesis of Absinthin J. Am. Chem. Soc. 2005, 127, 18-19 10.1021/ja0439219
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 18-19
-
-
Zhang, W.1
Luo, S.2
Chen, Q.3
Hu, H.4
Jia, X.5
Zhai, H.6
Fang7
-
80
-
-
0001172590
-
The Structure of Yingzhaosu
-
Liang, X. T.; Yu, D. Q.; Wu, W. L.; Deng, H. C. The Structure of Yingzhaosu Acta Chim. Sin. 1979, 37, 215-230
-
(1979)
Acta Chim. Sin.
, vol.37
, pp. 215-230
-
-
Liang, X.T.1
Yu, D.Q.2
Wu, W.L.3
Deng, H.C.4
-
81
-
-
0025948352
-
Total synthesis of (+)-Yingzhaosu A
-
Xu, X.-X.; Zhu, J.; Huang, D.-Z.; Zhou, W.-S. Total synthesis of (+)-Yingzhaosu A Tetrahedron Lett. 1991, 32, 5785-5788 10.1016/S0040-4039(00)93555-X
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5785-5788
-
-
Xu, X.-X.1
Zhu, J.2
Huang, D.-Z.3
Zhou, W.-S.4
-
82
-
-
17744377209
-
Total Syntheses of Yingzhaosu A and of Its C(14)-Epimer Including the First Evaluation of Their Antimalarial and Cytotoxic Activities
-
Szpilman, A. M.; Korshin, E. E.; Rozenberg, H.; Bachi, M. D. Total Syntheses of Yingzhaosu A and of Its C(14)-Epimer Including the First Evaluation of Their Antimalarial and Cytotoxic Activities J. Org. Chem. 2005, 70, 3618-3632 10.1021/jo050074z
-
(2005)
J. Org. Chem.
, vol.70
, pp. 3618-3632
-
-
Szpilman, A.M.1
Korshin, E.E.2
Rozenberg, H.3
Bachi, M.D.4
-
83
-
-
84882949864
-
The Impact of the Mukaiyama Aldol Reaction in Total Synthesis
-
Kan, S. B. J.; Ng, K. K.-H.; Paterson, I. The Impact of the Mukaiyama Aldol Reaction in Total Synthesis Angew. Chem., Int. Ed. 2013, 52, 9097-9108 10.1002/anie.201303914
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 9097-9108
-
-
Kan, S.B.J.1
Ng, K.K.-H.2
Paterson, I.3
-
84
-
-
0032541271
-
Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
-
Corey, E. J.; Helal, C. J. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method Angew. Chem., Int. Ed. 1998, 37, 1986-2012 10.1002/(SICI)1521-3773(19980817)37:15<1986::AID-ANIE1986>3.0.CO;2-Z
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 1986-2012
-
-
Corey, E.J.1
Helal, C.J.2
-
85
-
-
0002548130
-
The Peroxide Changes Everything: New Methodology for the Synthesis of Peroxide-Containing Natural Products
-
Dussault, P. The Peroxide Changes Everything: New Methodology for the Synthesis of Peroxide-Containing Natural Products Synlett 1995, 997-1003 10.1055/s-1995-5154
-
(1995)
Synlett
, pp. 997-1003
-
-
Dussault, P.1
-
86
-
-
84878118528
-
Synthesis of cis- and trans-Davanoids: Artemone, Hydroxydavanone, Isodavanone, and Nordavanone
-
Wan, K. K.; Evans-Klock, C. D.; Fielder, B. C.; Vosburg, D. A. Synthesis of cis- and trans-Davanoids: Artemone, Hydroxydavanone, Isodavanone, and Nordavanone Synthesis 2013, 45, 1541-1545 10.1055/s-0033-1338429
-
(2013)
Synthesis
, vol.45
, pp. 1541-1545
-
-
Wan, K.K.1
Evans-Klock, C.D.2
Fielder, B.C.3
Vosburg, D.A.4
-
87
-
-
84939572306
-
Direct, Biomimetic Synthesis of (+)-Artemone via a Stereoselective, Organocatalytic Cyclization
-
Nacsa, E. D.; Fielder, B. C.; Wetzler, S. P.; Srisuknimit, V.; Litz, J. P.; Van Vleet, M. J.; Quach, K.; Vosburg, D. A. Direct, Biomimetic Synthesis of (+)-Artemone via a Stereoselective, Organocatalytic Cyclization Synthesis 2015, 47, 2599-2602 10.1055/s-0034-1380684
-
(2015)
Synthesis
, vol.47
, pp. 2599-2602
-
-
Nacsa, E.D.1
Fielder, B.C.2
Wetzler, S.P.3
Srisuknimit, V.4
Litz, J.P.5
Van Vleet, M.J.6
Quach, K.7
Vosburg, D.A.8
-
88
-
-
0012533160
-
Structure and synthesis of Artemone
-
Naegeli, P.; Klimes, J.; Weber, G. Structure and synthesis of Artemone Tetrahedron Lett. 1970, 11, 5021-5024 10.1016/S0040-4039(00)89336-3
-
(1970)
Tetrahedron Lett.
, vol.11
, pp. 5021-5024
-
-
Naegeli, P.1
Klimes, J.2
Weber, G.3
-
89
-
-
0013535424
-
Stereoselective Syntheses of (+)-Davanone and (+)-Artemone via Anti-Selective Epoxidation and Iodo-cyclization
-
Honda, Y.; Ori, A.; Tsuchihashi, G.-I. Stereoselective Syntheses of (+)-Davanone and (+)-Artemone via Anti-Selective Epoxidation and Iodo-cyclization Chem. Lett. 1987, 16, 1259-1262 10.1246/cl.1987.1259
-
(1987)
Chem. Lett.
, vol.16
, pp. 1259-1262
-
-
Honda, Y.1
Ori, A.2
Tsuchihashi, G.-I.3
-
90
-
-
84858633852
-
The Diarylprolinol Silyl Ether System: A General Organocatalyst
-
Jensen, K. L.; Dickmeiss, G.; Jiang, H.; Albrecht, L.; Jørgensen, K. A. The Diarylprolinol Silyl Ether System: A General Organocatalyst Acc. Chem. Res. 2012, 45, 248-264 10.1021/ar200149w
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 248-264
-
-
Jensen, K.L.1
Dickmeiss, G.2
Jiang, H.3
Albrecht, L.4
Jørgensen, K.A.5
-
91
-
-
72849114754
-
Organozinc Generation via the Titanium-Catalyzed Activation of Alkyl Halides
-
Fleury, L. M.; Ashfeld, B. L. Organozinc Generation via the Titanium-Catalyzed Activation of Alkyl Halides Org. Lett. 2009, 11, 5670-5673 10.1021/ol902374v
-
(2009)
Org. Lett.
, vol.11
, pp. 5670-5673
-
-
Fleury, L.M.1
Ashfeld, B.L.2
-
92
-
-
0033678111
-
Sesquiterpenes from the Basidiomycete Omphalotus illudens
-
McMorris, T. C.; Lira, R.; Gantzel, P. K.; Kelner, M. J.; Dawe, R. Sesquiterpenes from the Basidiomycete Omphalotus illudens J. Nat. Prod. 2000, 63, 1557-1559 10.1021/np9904760
-
(2000)
J. Nat. Prod.
, vol.63
, pp. 1557-1559
-
-
McMorris, T.C.1
Lira, R.2
Gantzel, P.K.3
Kelner, M.J.4
Dawe, R.5
-
93
-
-
57149120359
-
New sesquiterpenes from Edible Fungus Clavicorona pyxidata
-
Zheng, Y.-B.; Lu, C.-H.; Zheng, Z.-H.; Lin, X.-J.; Su, W.-J.; Shen, Y.-M. New sesquiterpenes from Edible Fungus Clavicorona pyxidata Helv. Chim. Acta 2008, 91, 2174-2180 10.1002/hlca.200890235
-
(2008)
Helv. Chim. Acta
, vol.91
, pp. 2174-2180
-
-
Zheng, Y.-B.1
Lu, C.-H.2
Zheng, Z.-H.3
Lin, X.-J.4
Su, W.-J.5
Shen, Y.-M.6
-
94
-
-
84882319205
-
Natural sesquiterpenoids
-
Fraga, B. M. Natural sesquiterpenoids Nat. Prod. Rep. 2013, 30, 1226-1264 10.1039/c3np70047j
-
(2013)
Nat. Prod. Rep.
, vol.30
, pp. 1226-1264
-
-
Fraga, B.M.1
-
95
-
-
79961223193
-
Total Synthesis of (+)-Omphadiol
-
Liu, G.; Romo, D. Total Synthesis of (+)-Omphadiol Angew. Chem., Int. Ed. 2011, 50, 7537-7540 10.1002/anie.201102289
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7537-7540
-
-
Liu, G.1
Romo, D.2
-
96
-
-
33749027460
-
Bicyclic- and Tricyclic-β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin
-
Henry-Riyad, H.; Lee, C.; Purohit, V. C.; Romo, D. Bicyclic- and Tricyclic-β-lactones via Organonucleophile-Promoted Bis-Cyclizations of Keto Acids: Enantioselective Synthesis of (+)-Dihydroplakevulin Org. Lett. 2006, 8, 4363 10.1021/ol061816t
-
(2006)
Org. Lett.
, vol.8
, pp. 4363
-
-
Henry-Riyad, H.1
Lee, C.2
Purohit, V.C.3
Romo, D.4
-
97
-
-
77949595728
-
Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
-
Vougioukalakis, G. C.; Grubbs, R. H. Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts Chem. Rev. 2010, 110, 1746-1787 10.1021/cr9002424
-
(2010)
Chem. Rev.
, vol.110
, pp. 1746-1787
-
-
Vougioukalakis, G.C.1
Grubbs, R.H.2
-
98
-
-
36348935544
-
Bolivianine, a New Sesterpene with an Unusual Skeleton from Hedyosmum angustifolium, and Its Isomer, Isobolivianine
-
Acebey, L.; Sauvain, M.; Beck, S.; Moulis, C.; Gimenez, A.; Jullian, V. Bolivianine, a New Sesterpene with an Unusual Skeleton from Hedyosmum angustifolium, and Its Isomer, Isobolivianine Org. Lett. 2007, 9, 4693-4696 10.1021/ol7015725
-
(2007)
Org. Lett.
, vol.9
, pp. 4693-4696
-
-
Acebey, L.1
Sauvain, M.2
Beck, S.3
Moulis, C.4
Gimenez, A.5
Jullian, V.6
-
99
-
-
84897618824
-
Asymmetric Total Synthesis of Onoseriolide, Bolivianine, and Isobolivianine
-
Du, B.; Yuan, C.; Yu, T.; Yang, L.; Yang, Y.; Liu, B.; Qin, S. Asymmetric Total Synthesis of Onoseriolide, Bolivianine, and Isobolivianine Chem.-Eur. J. 2014, 20, 2613-2622 10.1002/chem.201304378
-
(2014)
Chem. - Eur. J.
, vol.20
, pp. 2613-2622
-
-
Du, B.1
Yuan, C.2
Yu, T.3
Yang, L.4
Yang, Y.5
Liu, B.6
Qin, S.7
-
100
-
-
84879510518
-
Bioinspired Total Synthesis of Bolivianine: A Diels- Alder/ Intramolecular Hetero-Diels-Alder Cascade Approach
-
Yuan, C.; Du, B.; Yang, L.; Liu, B. Bioinspired Total Synthesis of Bolivianine: A Diels- Alder/ Intramolecular Hetero-Diels-Alder Cascade Approach J. Am. Chem. Soc. 2013, 135, 9291-9294 10.1021/ja4040335
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 9291-9294
-
-
Yuan, C.1
Du, B.2
Yang, L.3
Liu, B.4
-
101
-
-
0000666915
-
Efficient Synthesis of (lS,5S)-4-Alkyl-6,6-dimethylbicyclo[3.1.1]hept-3-en-2-ones from (1R,5S)-(+)-Nopinone and Preparation of Some Chiral Building Blocks Suitable for the Asymmetric Synthesis
-
Watanabe, M.; Awen, B. Z.; Kato, M. Efficient Synthesis of (lS,5S)-4-Alkyl-6,6-dimethylbicyclo[3.1.1]hept-3-en-2-ones from (1R,5S)-(+)-Nopinone and Preparation of Some Chiral Building Blocks Suitable for the Asymmetric Synthesis J. Org. Chem. 1993, 58, 3923-3927 10.1021/jo00067a026
-
(1993)
J. Org. Chem.
, vol.58
, pp. 3923-3927
-
-
Watanabe, M.1
Awen, B.Z.2
Kato, M.3
-
102
-
-
18144398606
-
The Use of Tosylhydrazone Salts as a Safe Alternative for Handling Diazo Compounds and Their Applications in Organic Synthesis
-
Fulton, J. R.; Aggarwal, V. K.; de Vicente, J. The Use of Tosylhydrazone Salts as a Safe Alternative for Handling Diazo Compounds and Their Applications in Organic Synthesis Eur. J. Org. Chem. 2005, 1479-1492 10.1002/ejoc.200400700
-
(2005)
Eur. J. Org. Chem.
, pp. 1479-1492
-
-
Fulton, J.R.1
Aggarwal, V.K.2
De Vicente, J.3
-
103
-
-
18444417883
-
Catalytic methods for metal carbene transformations
-
Doyle, M. P. Catalytic methods for metal carbene transformations Chem. Rev. 1986, 86, 919-939 10.1021/cr00075a013
-
(1986)
Chem. Rev.
, vol.86
, pp. 919-939
-
-
Doyle, M.P.1
-
104
-
-
3042745794
-
Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products
-
Oikawa, H.; Tokiwano, T. Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products Nat. Prod. Rep. 2004, 21, 321-352 10.1039/B305068H
-
(2004)
Nat. Prod. Rep.
, vol.21
, pp. 321-352
-
-
Oikawa, H.1
Tokiwano, T.2
-
105
-
-
0041810236
-
Chemistry and Biology of Biosynthetic Diels-Alder Reactions
-
Stocking, E. M.; Williams, R. M. Chemistry and Biology of Biosynthetic Diels-Alder Reactions Angew. Chem., Int. Ed. 2003, 42, 3078-3115 10.1002/anie.200200534
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3078-3115
-
-
Stocking, E.M.1
Williams, R.M.2
-
106
-
-
84948808336
-
Natural Diels-Alderases: Elusive and Irresistible
-
Klas, K.; Tsukamoto, S.; Sherman, D. H.; Williams, R. M. Natural Diels-Alderases: Elusive and Irresistible J. Org. Chem. 2015, 80, 11672-11685 10.1021/acs.joc.5b01951
-
(2015)
J. Org. Chem.
, vol.80
, pp. 11672-11685
-
-
Klas, K.1
Tsukamoto, S.2
Sherman, D.H.3
Williams, R.M.4
-
107
-
-
0036259981
-
The Diels-Alder Reaction in Total Synthesis
-
Nicolaou, K. C.; Snyder, S. A.; Montagnon, T.; Vassilikogiannakis, G. The Diels-Alder Reaction in Total Synthesis Angew. Chem., Int. Ed. 2002, 41, 1668-1698 10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 1668-1698
-
-
Nicolaou, K.C.1
Snyder, S.A.2
Montagnon, T.3
Vassilikogiannakis, G.4
-
108
-
-
34047246977
-
Chemistry and neurotrophic activity of seco-prezizaane- and anislactone-type sesquiterpenes from Illicium species
-
Atta-ur-Rahman, Elsevier: Amsterdam
-
Fukuyama, Y.; Huang, J.-M. Chemistry and neurotrophic activity of seco-prezizaane- and anislactone-type sesquiterpenes from Illicium species. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 2005; Vol. 32, pp 395-429.
-
(2005)
Studies in Natural Products Chemistry
, vol.32
, pp. 395-429
-
-
Fukuyama, Y.1
Huang, J.-M.2
-
109
-
-
70749119799
-
Novel Pentacyclic seco-Prezizaane-Type Sesquiterpenoids with Neurotrophic Properties from Illicium jiadifengpi
-
Kubo, M.; Okada, C.; Huang, J.-M.; Harada, K.; Hioki, H.; Fukuyama, Y. Novel Pentacyclic seco-Prezizaane-Type Sesquiterpenoids with Neurotrophic Properties from Illicium jiadifengpi Org. Lett. 2009, 11, 5190-5193 10.1021/ol9021029
-
(2009)
Org. Lett.
, vol.11
, pp. 5190-5193
-
-
Kubo, M.1
Okada, C.2
Huang, J.-M.3
Harada, K.4
Hioki, H.5
Fukuyama, Y.6
-
110
-
-
79953727555
-
Enantioselective Total Synthesis of (-)-Jiadifenolide
-
Xu, J.; Trzoss, L.; Chang, W. K.; Theodorakis, E. A. Enantioselective Total Synthesis of (-)-Jiadifenolide Angew. Chem., Int. Ed. 2011, 50, 3672-3676 10.1002/anie.201100313
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 3672-3676
-
-
Xu, J.1
Trzoss, L.2
Chang, W.K.3
Theodorakis, E.A.4
-
111
-
-
84877310324
-
Illicium Sesquiterpenes: Divergent Synthetic Strategy and Neurotrophic Activity Studies
-
Trzoss, L.; Xu, J.; Lacoske, M. H.; Mobley, W. C.; Theodorakis, E. A. Illicium Sesquiterpenes: Divergent Synthetic Strategy and Neurotrophic Activity Studies Chem.-Eur. J. 2013, 19, 6398-6408 10.1002/chem.201300198
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 6398-6408
-
-
Trzoss, L.1
Xu, J.2
Lacoske, M.H.3
Mobley, W.C.4
Theodorakis, E.A.5
-
112
-
-
84903719573
-
Total Synthesis of Jiadifenolide
-
Paterson, I.; Xuan, M.; Dalby, S. M. Total Synthesis of Jiadifenolide Angew. Chem., Int. Ed. 2014, 53, 7286-7289 10.1002/anie.201404224
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 7286-7289
-
-
Paterson, I.1
Xuan, M.2
Dalby, S.M.3
-
113
-
-
84900855264
-
An Enantiospecific Synthesis of Jiadifenolide
-
Siler, D. A.; Mighion, J. D.; Sorensen, E. J. An Enantiospecific Synthesis of Jiadifenolide Angew. Chem., Int. Ed. 2014, 53, 5332-5335 10.1002/anie.201402335
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 5332-5335
-
-
Siler, D.A.1
Mighion, J.D.2
Sorensen, E.J.3
-
114
-
-
84932605974
-
An eight-step gram-scale synthesis of (-)-jiadifenolide
-
Lu, H.-H.; Martinez, M. D.; Shenvi, R. A. An eight-step gram-scale synthesis of (-)-jiadifenolide Nat. Chem. 2015, 7, 604-607 10.1038/nchem.2283
-
(2015)
Nat. Chem.
, vol.7
, pp. 604-607
-
-
Lu, H.-H.1
Martinez, M.D.2
Shenvi, R.A.3
-
115
-
-
84946771574
-
Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans
-
Shen, Y.; Li, L.; Pan, Z.; Wang, Y.; Li, J.; Wang, K.; Wang, X.; Zhang, Y.; Hu, T.; Zhang, Y. Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans Org. Lett. 2015, 17, 5480-5483 10.1021/acs.orglett.5b02845
-
(2015)
Org. Lett.
, vol.17
, pp. 5480-5483
-
-
Shen, Y.1
Li, L.2
Pan, Z.3
Wang, Y.4
Li, J.5
Wang, K.6
Wang, X.7
Zhang, Y.8
Hu, T.9
Zhang, Y.10
-
116
-
-
84996542592
-
Formal Total Synthesis of (-)-Jiadifenolide and Synthetic Studies toward seco-Prezizaane-Type Sesquiterpenes
-
Gomes, J.; Daeppen, C.; Liffert, R.; Roesslein, J.; Kaufmann, E.; Heikinheimo, A.; Neuburger, M.; Gademann, K. J. Formal Total Synthesis of (-)-Jiadifenolide and Synthetic Studies toward seco-Prezizaane-Type Sesquiterpenes J. Org. Chem. 2016, 81, 11017-11034 10.1021/acs.joc.6b02039
-
(2016)
J. Org. Chem.
, vol.81
, pp. 11017-11034
-
-
Gomes, J.1
Daeppen, C.2
Liffert, R.3
Roesslein, J.4
Kaufmann, E.5
Heikinheimo, A.6
Neuburger, M.7
Gademann, K.J.8
-
117
-
-
0011225923
-
The Favorskii Rearrangement of Pulegone Dibromide
-
Wolinsky, J.; Chan, D. The Favorskii Rearrangement of Pulegone Dibromide J. Org. Chem. 1965, 30, 41-43 10.1021/jo01012a008
-
(1965)
J. Org. Chem.
, vol.30
, pp. 41-43
-
-
Wolinsky, J.1
Chan, D.2
-
118
-
-
0343610582
-
Total Synthesis of (-)-Prezizaene and (-)-Prezizanol
-
Vettel, P. R.; Coates, R. M. Total Synthesis of (-)-Prezizaene and (-)-Prezizanol J. Org. Chem. 1980, 45, 5430-5432 10.1021/jo01314a062
-
(1980)
J. Org. Chem.
, vol.45
, pp. 5430-5432
-
-
Vettel, P.R.1
Coates, R.M.2
-
119
-
-
0002062240
-
The Robinson Annelation and Related Reactions
-
Gawley, R. E. The Robinson Annelation and Related Reactions Synthesis 1976, 1976, 777-794 10.1055/s-1976-24200
-
(1976)
Synthesis
, vol.1976
, pp. 777-794
-
-
Gawley, R.E.1
-
120
-
-
0025689296
-
Stereocontrolled Total Synthesis of (-)-Anisatin: A Neurotoxic Sesquiterpenoid Possessing a Novel Spiro β-Lactone
-
Niwa, H.; Nisiwaki, M.; Tsukada, I.; Ishigaki, T.; Ito, S.; Wakamatsu, K.; Mori, T.; Ikagawa, M.; Yamada, K. Stereocontrolled Total Synthesis of (-)-Anisatin: A Neurotoxic Sesquiterpenoid Possessing a Novel Spiro β-Lactone J. Am. Chem. Soc. 1990, 112, 9001-9003 10.1021/ja00180a067
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 9001-9003
-
-
Niwa, H.1
Nisiwaki, M.2
Tsukada, I.3
Ishigaki, T.4
Ito, S.5
Wakamatsu, K.6
Mori, T.7
Ikagawa, M.8
Yamada, K.9
-
121
-
-
0000243566
-
Synthetic Uses of Tosylmethyl Isocyanide (TosMIC)
-
Leusen, D. V.; Leusen, A. M. V. Synthetic Uses of Tosylmethyl Isocyanide (TosMIC) Organic Reactions. 2001, 57 (3) 417-666 10.1002/0471264180.or057.03
-
(2001)
Organic Reactions.
, vol.57
, Issue.3
, pp. 417-666
-
-
Leusen, D.V.1
Leusen, A.M.V.2
-
123
-
-
75749134825
-
O-Acetyl Oximes as Transformable Directing Groups for Pd-Catalyzed C-H Bond Functionalization
-
Neufeldt, S. R.; Sanford, M. S. O-Acetyl Oximes as Transformable Directing Groups for Pd-Catalyzed C-H Bond Functionalization Org. Lett. 2010, 12, 532-535 10.1021/ol902720d
-
(2010)
Org. Lett.
, vol.12
, pp. 532-535
-
-
Neufeldt, S.R.1
Sanford, M.S.2
-
124
-
-
77949381429
-
Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions
-
Lyons, T. W.; Sanford, M. S. Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions Chem. Rev. 2010, 110, 1147-1169 10.1021/cr900184e
-
(2010)
Chem. Rev.
, vol.110
, pp. 1147-1169
-
-
Lyons, T.W.1
Sanford, M.S.2
-
125
-
-
79958774552
-
C-H functionalization logic in total synthesis
-
Gutekunst, W. R.; Baran, P. S. C-H functionalization logic in total synthesis Chem. Soc. Rev. 2011, 40, 1976-1991 10.1039/c0cs00182a
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 1976-1991
-
-
Gutekunst, W.R.1
Baran, P.S.2
-
126
-
-
84864120575
-
C-H Activation: A Complementary Tool in the Total Synthesis of Complex Natural Products
-
Chen, D. Y.-K.; Youn, S. W. C-H Activation: A Complementary Tool in the Total Synthesis of Complex Natural Products Chem.-Eur. J. 2012, 18, 9452-9474 10.1002/chem.201201329
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 9452-9474
-
-
Chen, D.Y.-K.1
Youn, S.W.2
-
127
-
-
84863496539
-
Innate and Guided C-H Functionalization Logic
-
Brückl, T.; Baxter, R. D.; Ishihara, Y.; Baran, P. S. Innate and Guided C-H Functionalization Logic Acc. Chem. Res. 2012, 45, 826-839 10.1021/ar200194b
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 826-839
-
-
Brückl, T.1
Baxter, R.D.2
Ishihara, Y.3
Baran, P.S.4
-
128
-
-
84865838463
-
C-H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
-
Yamaguchi, J.; Yamaguchi, A. D.; Itami, K. C-H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals Angew. Chem., Int. Ed. 2012, 51, 8960-9009 10.1002/anie.201201666
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 8960-9009
-
-
Yamaguchi, J.1
Yamaguchi, A.D.2
Itami, K.3
-
129
-
-
84954528833
-
Evolution of C-H Bond Functionalization from Methane to Methodology
-
Hartwig, J. F. Evolution of C-H Bond Functionalization from Methane to Methodology J. Am. Chem. Soc. 2016, 138, 2-24 10.1021/jacs.5b08707
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 2-24
-
-
Hartwig, J.F.1
-
130
-
-
84982787058
-
C-H bond activation in the total syntheses of natural products
-
Tao, P.; Jia, Y. C-H bond activation in the total syntheses of natural products Sci. China: Chem. 2016, 59, 1109-1125 10.1007/s11426-016-0058-7
-
(2016)
Sci. China: Chem.
, vol.59
, pp. 1109-1125
-
-
Tao, P.1
Jia, Y.2
-
131
-
-
2142715741
-
Sequencing Reactions with Samarium(II) Iodide
-
Molander, G. A.; Harris, C. R. Sequencing Reactions with Samarium(II) Iodide Chem. Rev. 1996, 96, 307-338 10.1021/cr950019y
-
(1996)
Chem. Rev.
, vol.96
, pp. 307-338
-
-
Molander, G.A.1
Harris, C.R.2
-
132
-
-
3543057490
-
Samarium(II)-Iodide-Mediated Cyclizations in Natural Product Synthesis
-
Edmonds, D. J.; Johnston, D.; Procter, D. J. Samarium(II)-Iodide-Mediated Cyclizations in Natural Product Synthesis Chem. Rev. 2004, 104, 3371-3404 10.1021/cr030017a
-
(2004)
Chem. Rev.
, vol.104
, pp. 3371-3404
-
-
Edmonds, D.J.1
Johnston, D.2
Procter, D.J.3
-
133
-
-
70349922853
-
Samarium diiodide mediated reactions in total synthesis
-
Nicolaou, K. C.; Ellery, S. P.; Chen, J. S. Samarium diiodide mediated reactions in total synthesis Angew. Chem., Int. Ed. 2009, 48, 7140-7165 10.1002/anie.200902151
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 7140-7165
-
-
Nicolaou, K.C.1
Ellery, S.P.2
Chen, J.S.3
-
134
-
-
62249212754
-
A general one-step synthesis of alkynes from enolisable carbonyl compounds
-
Lyapkalo, I. M.; Vogel, M. A. K.; Boltukhina, E. V.; Vavřík, J. A general one-step synthesis of alkynes from enolisable carbonyl compounds Synlett 2009, 558-561 10.1055/s-0028-1087919
-
(2009)
Synlett
, pp. 558-561
-
-
Lyapkalo, I.M.1
Vogel, M.A.K.2
Boltukhina, E.V.3
Vavřík, J.4
-
135
-
-
84878203380
-
Versatile synthesis of acylfuranones by reaction of acylketenes with α-hydroxy ketones: Application to the one-step multi-component synthesis of cadiolide B and its analogues
-
Peixoto, P. A.; Boulangé, A.; Leleu, S.; Franck, X. Versatile synthesis of acylfuranones by reaction of acylketenes with α-hydroxy ketones: application to the one-step multi-component synthesis of cadiolide B and its analogues Eur. J. Org. Chem. 2013, 3316-3327 10.1002/ejoc.201300166
-
(2013)
Eur. J. Org. Chem.
, pp. 3316-3327
-
-
Peixoto, P.A.1
Boulangé, A.2
Leleu, S.3
Franck, X.4
-
136
-
-
84896129354
-
Natural product synthesis in the age of scalability
-
Kuttruff, C. A.; Eastgate, M. D.; Baran, P. S. Natural product synthesis in the age of scalability Nat. Prod. Rep. 2014, 31, 419-432 10.1039/C3NP70090A
-
(2014)
Nat. Prod. Rep.
, vol.31
, pp. 419-432
-
-
Kuttruff, C.A.1
Eastgate, M.D.2
Baran, P.S.3
-
137
-
-
59649114569
-
Englerin A, a Selective Inhibitor of Renal Cancer Cell Growth, from Phyllanthus engleri
-
Ratnayake, R.; Covell, D.; Ransom, T. T.; Gustafson, K. R.; Beutler, J. A. Englerin A, a Selective Inhibitor of Renal Cancer Cell Growth, from Phyllanthus engleri Org. Lett. 2009, 11, 57-60 10.1021/ol802339w
-
(2009)
Org. Lett.
, vol.11
, pp. 57-60
-
-
Ratnayake, R.1
Covell, D.2
Ransom, T.T.3
Gustafson, K.R.4
Beutler, J.A.5
-
138
-
-
84255169377
-
Chemical Synthesis of the Englerins
-
Pouwer, R. H.; Richard, J.-A.; Tseng, C.-C.; Chen, D. Y.-K. Chemical Synthesis of the Englerins Chem.-Asian J. 2012, 7, 22-35 10.1002/asia.201100780
-
(2012)
Chem. - Asian J.
, vol.7
, pp. 22-35
-
-
Pouwer, R.H.1
Richard, J.-A.2
Tseng, C.-C.3
Chen, D.Y.-K.4
-
139
-
-
70449575812
-
Total Synthesis and Absolute Configuration of the Guaiane Sesquiterpene Englerin A
-
Willot, M.; Radtke, L.; Könning, D.; Fröhlich, R.; Gessner, V. H.; Strohmann, C.; Christmann, M. Total Synthesis and Absolute Configuration of the Guaiane Sesquiterpene Englerin A Angew. Chem., Int. Ed. 2009, 48, 9105-9108 10.1002/anie.200905032
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9105-9108
-
-
Willot, M.1
Radtke, L.2
Könning, D.3
Fröhlich, R.4
Gessner, V.H.5
Strohmann, C.6
Christmann, M.7
-
140
-
-
77953314970
-
Total Synthesis of Englerin A
-
Nicolaou, K. C.; Kang, Q.; Ng, S. Y.; Chen, D. Y.-K. Total Synthesis of Englerin A J. Am. Chem. Soc. 2010, 132, 8219-8222 10.1021/ja102927n
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8219-8222
-
-
Nicolaou, K.C.1
Kang, Q.2
Ng, S.Y.3
Chen, D.Y.-K.4
-
141
-
-
77955683809
-
Enantioselective Formal Synthesis of (-)-Englerin A via a Rh-Catalyzed [4 + 3] Cycloaddition Reaction
-
Xu, J.; Caro-Diaz, E. J. E.; Theodorakis, E. A. Enantioselective Formal Synthesis of (-)-Englerin A via a Rh-Catalyzed [4 + 3] Cycloaddition Reaction Org. Lett. 2010, 12, 3708-3711 10.1021/ol1015652
-
(2010)
Org. Lett.
, vol.12
, pp. 3708-3711
-
-
Xu, J.1
Caro-Diaz, E.J.E.2
Theodorakis, E.A.3
-
142
-
-
77952328004
-
Asymmetric, Protecting-Group-Free Total Synthesis of (-)-Englerin A
-
Zhou, Q.; Chen, X.; Ma, D. Asymmetric, Protecting-Group-Free Total Synthesis of (-)-Englerin A Angew. Chem., Int. Ed. 2010, 49, 3513-3516 10.1002/anie.201000888
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3513-3516
-
-
Zhou, Q.1
Chen, X.2
Ma, D.3
-
143
-
-
77952397509
-
Enantioselective Synthesis of (-)-Englerins A and B
-
Molawi, K.; Delpont, N.; Echavarren, A. M. Enantioselective Synthesis of (-)-Englerins A and B Angew. Chem., Int. Ed. 2010, 49, 3517-3519 10.1002/anie.201000890
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3517-3519
-
-
Molawi, K.1
Delpont, N.2
Echavarren, A.M.3
-
144
-
-
79955461496
-
A Brief Synthesis of (-)-Englerin A
-
Li, Z.; Nakashige, M.; Chain, W. J. A Brief Synthesis of (-)-Englerin A J. Am. Chem. Soc. 2011, 133, 6553-6556 10.1021/ja201921j
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 6553-6556
-
-
Li, Z.1
Nakashige, M.2
Chain, W.J.3
-
145
-
-
84866091995
-
Stereocontrolled Total Synthesis of (-)-Englerin A
-
Takahashi, K.; Komine, K.; Yokoi, Y.; Ishihara, J.; Hatakeyama, S. Stereocontrolled Total Synthesis of (-)-Englerin A J. Org. Chem. 2012, 77, 7364-7370 10.1021/jo301145r
-
(2012)
J. Org. Chem.
, vol.77
, pp. 7364-7370
-
-
Takahashi, K.1
Komine, K.2
Yokoi, Y.3
Ishihara, J.4
Hatakeyama, S.5
-
146
-
-
84861796587
-
A Formal Synthesis of (-)-Englerin A by Relay Ring Closing Metathesis and Transannular Etherification
-
Lee, J.; Parker, K. A. A Formal Synthesis of (-)-Englerin A by Relay Ring Closing Metathesis and Transannular Etherification Org. Lett. 2012, 14, 2682-2685 10.1021/ol3007524
-
(2012)
Org. Lett.
, vol.14
, pp. 2682-2685
-
-
Lee, J.1
Parker, K.A.2
-
147
-
-
84863617622
-
A Reductive-Heck Approach to the Hydroazulene Ring System: A Formal Synthesis of the Englerins
-
Gao, P.; Cook, S. P. A Reductive-Heck Approach to the Hydroazulene Ring System: A Formal Synthesis of the Englerins Org. Lett. 2012, 14, 3340-3343 10.1021/ol3013167
-
(2012)
Org. Lett.
, vol.14
, pp. 3340-3343
-
-
Gao, P.1
Cook, S.P.2
-
148
-
-
84877256728
-
A Short Enantioselective Total Synthesis of (-)-Englerin A
-
Zahel, M.; Keßberg, A.; Metz, P. A Short Enantioselective Total Synthesis of (-)-Englerin A Angew. Chem., Int. Ed. 2013, 52, 5390-5392 10.1002/anie.201301247
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 5390-5392
-
-
Zahel, M.1
Keßberg, A.2
Metz, P.3
-
149
-
-
84873343839
-
Collective Total Synthesis of Englerin A and B, Orientalol e and F, and Oxyphyllol: Application of the Organocatalytic [4 + 3] Cycloaddition Reaction
-
Wang, J.; Chen, S.-G.; Sun, B.-F.; Lin, G.-Q.; Shang, Y.-J. Collective Total Synthesis of Englerin A and B, Orientalol E and F, and Oxyphyllol: Application of the Organocatalytic [4 + 3] Cycloaddition Reaction Chem.-Eur. J. 2013, 19, 2539-2547 10.1002/chem.201203467
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 2539-2547
-
-
Wang, J.1
Chen, S.-G.2
Sun, B.-F.3
Lin, G.-Q.4
Shang, Y.-J.5
-
150
-
-
84893792247
-
Total synthesis of (-)-Englerin A
-
Zhang, J.; Zheng, S.; Peng, W.; Shen, Z. Total synthesis of (-)-Englerin A Tetrahedron Lett. 2014, 55, 1339-1341 10.1016/j.tetlet.2014.01.012
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 1339-1341
-
-
Zhang, J.1
Zheng, S.2
Peng, W.3
Shen, Z.4
-
151
-
-
84938379137
-
Asymmetric Total Synthesis of (-)-Englerin A through Catalytic Diastereo- and Enantioselective Carbonyl Ylide Cycloaddition
-
Hanari, T.; Shimada, N.; Kurosaki, Y.; Thrimurtulu, N.; Nambu, H.; Anada, M.; Hashimoto, S. Asymmetric Total Synthesis of (-)-Englerin A through Catalytic Diastereo- and Enantioselective Carbonyl Ylide Cycloaddition Chem.-Eur. J. 2015, 21, 11671-11676 10.1002/chem.201502009
-
(2015)
Chem. - Eur. J.
, vol.21
, pp. 11671-11676
-
-
Hanari, T.1
Shimada, N.2
Kurosaki, Y.3
Thrimurtulu, N.4
Nambu, H.5
Anada, M.6
Hashimoto, S.7
-
152
-
-
84954052576
-
Total Synthesis of (±)-Englerin A Using An Intermolecular [3 + 2] Cycloaddition Reaction of Platinum-Containing Carbonyl Ylide
-
Kusama, H.; Tazawa, A.; Ishida, K.; Iwasawa, N. Total Synthesis of (±)-Englerin A Using An Intermolecular [3 + 2] Cycloaddition Reaction of Platinum-Containing Carbonyl Ylide Chem.-Asian J. 2016, 11, 64-67 10.1002/asia.201500935
-
(2016)
Chem. - Asian J.
, vol.11
, pp. 64-67
-
-
Kusama, H.1
Tazawa, A.2
Ishida, K.3
Iwasawa, N.4
-
153
-
-
84991384085
-
Concise, Enantioselective, and Versatile Synthesis of (-)-Englerin A Based on a Platinum-Catalyzed [4C+3C] Cycloaddition of Allenedienes
-
Nelson, R.; Gulías, M.; Mascarenas, J. L.; López, F. Concise, Enantioselective, and Versatile Synthesis of (-)-Englerin A Based on a Platinum-Catalyzed [4C+3C] Cycloaddition of Allenedienes Angew. Chem., Int. Ed. 2016, 55, 14359-14363 10.1002/anie.201607348
-
(2016)
Angew. Chem., Int. Ed.
, vol.55
, pp. 14359-14363
-
-
Nelson, R.1
Gulías, M.2
Mascarenas, J.L.3
López, F.4
-
154
-
-
0002863020
-
A Convenient One-flask Synthesis of α-Methylenealdehydes from Primary Alcohols
-
Takano, S.; Inomata, K.; Samizu, K.; Tomita, S.; Yanase, M.; Suzuki, M.; Iwabuchi, Y.; Sugihara, T.; Ogasawara, K. A Convenient One-flask Synthesis of α-Methylenealdehydes from Primary Alcohols Chem. Lett. 1989, 18, 1283-1284 10.1246/cl.1989.1283
-
(1989)
Chem. Lett.
, vol.18
, pp. 1283-1284
-
-
Takano, S.1
Inomata, K.2
Samizu, K.3
Tomita, S.4
Yanase, M.5
Suzuki, M.6
Iwabuchi, Y.7
Sugihara, T.8
Ogasawara, K.9
-
155
-
-
0141630721
-
Catalyst-Controlled Inverse-Electron-Demand Hetero-Diels-Alder Reactions in the Enantio- and Diastereoselective Synthesis of Iridoid Natural Products
-
Chavez, D. E.; Jacobsen, E. N. Catalyst-Controlled Inverse-Electron-Demand Hetero-Diels-Alder Reactions in the Enantio- and Diastereoselective Synthesis of Iridoid Natural Products Org. Lett. 2003, 5, 2563-2565 10.1021/ol034883l
-
(2003)
Org. Lett.
, vol.5
, pp. 2563-2565
-
-
Chavez, D.E.1
Jacobsen, E.N.2
-
156
-
-
0001616071
-
A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization
-
Inanaga, J.; Hirata, K.; Saeki, H.; Katsuki, T.; Yamaguchi, M. A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring Lactonization Bull. Chem. Soc. Jpn. 1979, 52, 1989-1993 10.1246/bcsj.52.1989
-
(1979)
Bull. Chem. Soc. Jpn.
, vol.52
, pp. 1989-1993
-
-
Inanaga, J.1
Hirata, K.2
Saeki, H.3
Katsuki, T.4
Yamaguchi, M.5
-
157
-
-
70449356896
-
Organocatalyzed Tsuji-Trost reaction: A new method for the closure of five- and six-membered rings
-
Vulovic, B.; Bihelovic, F.; Matovic, R.; Saicic, R. N. Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings Tetrahedron 2009, 65, 10485-10494 10.1016/j.tet.2009.10.006
-
(2009)
Tetrahedron
, vol.65
, pp. 10485-10494
-
-
Vulovic, B.1
Bihelovic, F.2
Matovic, R.3
Saicic, R.N.4
-
158
-
-
41849127508
-
Recent advances in the total synthesis of pharmaceutically relevant diterpenes
-
Busch, T.; Kirschning, A. Recent advances in the total synthesis of pharmaceutically relevant diterpenes Nat. Prod. Rep. 2008, 25, 318-341 10.1039/b705652b
-
(2008)
Nat. Prod. Rep.
, vol.25
, pp. 318-341
-
-
Busch, T.1
Kirschning, A.2
-
159
-
-
0346362506
-
Pyranophane Transannular Diels-Alder Approach to (+)-Chatancin: A Biomimetic Asymmetric Total Synthesis
-
Soucy, P.; L' Heureux, A.; Toró, A.; Deslongchamps, P. Pyranophane Transannular Diels-Alder Approach to (+)-Chatancin: A Biomimetic Asymmetric Total Synthesis J. Org. Chem. 2003, 68, 9983-9987 10.1021/jo035193y
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9983-9987
-
-
Soucy, P.1
L'Heureux, A.2
Toró, A.3
Deslongchamps, P.4
-
160
-
-
0038547883
-
Enantioselective Total Synthesis of Briarellins e and F: The First Total Syntheses of Briarellin Diterpenes
-
Corminboeuf, O.; Overman, L. E.; Pennington, L. D. Enantioselective Total Synthesis of Briarellins E and F: The First Total Syntheses of Briarellin Diterpenes J. Am. Chem. Soc. 2003, 125, 6650-6652 10.1021/ja035445c
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6650-6652
-
-
Corminboeuf, O.1
Overman, L.E.2
Pennington, L.D.3
-
161
-
-
33744820817
-
Convergent, Enantioselective Syntheses of Guanacastepenes A and e Featuring a Selective Cyclobutane Fragmentation
-
Shipe, W. D.; Sorensen, E. J. Convergent, Enantioselective Syntheses of Guanacastepenes A and E Featuring a Selective Cyclobutane Fragmentation J. Am. Chem. Soc. 2006, 128, 7025-7035 10.1021/ja060847g
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 7025-7035
-
-
Shipe, W.D.1
Sorensen, E.J.2
-
162
-
-
64549097262
-
Total Synthesis of (-)-Platensimycin, a Novel Antibacterial Agent
-
Ghosh, A. K.; Xi, K. Total Synthesis of (-)-Platensimycin, a Novel Antibacterial Agent J. Org. Chem. 2009, 74, 1163-1170 10.1021/jo802261f
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1163-1170
-
-
Ghosh, A.K.1
Xi, K.2
-
163
-
-
15444364284
-
Total Synthesis of (-)-Colombiasin A and (-)-Elisapterosin B
-
Harrowven, D. C.; Pascoe, D. D.; Demurtas, D.; Bourne, H. O. Total Synthesis of (-)-Colombiasin A and (-)-Elisapterosin B Angew. Chem., Int. Ed. 2005, 44, 1221-1222 10.1002/anie.200462268
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 1221-1222
-
-
Harrowven, D.C.1
Pascoe, D.D.2
Demurtas, D.3
Bourne, H.O.4
-
164
-
-
0037442639
-
Total Synthesis of (+)-Phomactin A Using a B-Alkyl Suzuki Macrocyclization
-
Mohr, P. J.; Halcomb, R. L. Total Synthesis of (+)-Phomactin A Using a B-Alkyl Suzuki Macrocyclization J. Am. Chem. Soc. 2003, 125, 1712-1713 10.1021/ja0296531
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 1712-1713
-
-
Mohr, P.J.1
Halcomb, R.L.2
-
165
-
-
51649114072
-
Short Formal Synthesis of (-)-Platencin
-
Tiefenbacher, K.; Mulzer, J. Short Formal Synthesis of (-)-Platencin Angew. Chem., Int. Ed. 2008, 47, 6199-6200 10.1002/anie.200801441
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6199-6200
-
-
Tiefenbacher, K.1
Mulzer, J.2
-
166
-
-
52449095155
-
High-Pressure Entry into Platencin
-
Waalboer, D. C. J.; Schaapman, M. C.; van Delft, F. L.; Rutjes, F. P. J. T. High-Pressure Entry into Platencin Angew. Chem., Int. Ed. 2008, 47, 6576-6578 10.1002/anie.200802912
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6576-6578
-
-
Waalboer, D.C.J.1
Schaapman, M.C.2
Van Delft, F.L.3
Rutjes, F.P.J.T.4
-
167
-
-
1242269274
-
Toward a General Route to the Eunicellin Diterpenes: The Asymmetric Total Synthesis of Deacetoxyalcyonin Acetate
-
Molander, G. A.; St. Jean, D. J., Jr.; Haas, J. Toward a General Route to the Eunicellin Diterpenes: The Asymmetric Total Synthesis of Deacetoxyalcyonin Acetate J. Am. Chem. Soc. 2004, 126, 1642-1643 10.1021/ja0398464
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 1642-1643
-
-
Molander, G.A.1
St. Jean, D.J.2
Haas, J.3
-
168
-
-
79955419320
-
Synthesis of ent-Nanolobatolide
-
Cheng, H. M.; Tian, W.; Peixoto, P. A.; Dhudshia, B.; Chen, D. Y.-K. Synthesis of ent-Nanolobatolide Angew. Chem., Int. Ed. 2011, 50, 4165-4168 10.1002/anie.201100926
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 4165-4168
-
-
Cheng, H.M.1
Tian, W.2
Peixoto, P.A.3
Dhudshia, B.4
Chen, D.Y.-K.5
-
169
-
-
36649034674
-
Total Syntheses and Synthetic Studies of Spongiane Diterpenes
-
González, M. A. Total Syntheses and Synthetic Studies of Spongiane Diterpenes Tetrahedron 2008, 64, 445-467 10.1016/j.tet.2007.10.057
-
(2008)
Tetrahedron
, vol.64
, pp. 445-467
-
-
González, M.A.1
-
170
-
-
0000906667
-
Diterpene Metabolites of the Marine Sponge Chelonaplysilla violacea: Aplyviolene and Aplyviolacene
-
Hambley, T. W.; Poiner, A.; Taylor, W. C. Diterpene Metabolites of the Marine Sponge Chelonaplysilla violacea: Aplyviolene and Aplyviolacene Tetrahedron Lett. 1986, 27, 3281-3282 10.1016/S0040-4039(00)84775-9
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 3281-3282
-
-
Hambley, T.W.1
Poiner, A.2
Taylor, W.C.3
-
171
-
-
0033842861
-
A new strategy for synthesis of attached rings
-
Overman, L. E.; Pennington, L. D. A new strategy for synthesis of attached rings Can. J. Chem. 2000, 78, 732-738 10.1139/v00-022
-
(2000)
Can. J. Chem.
, vol.78
, pp. 732-738
-
-
Overman, L.E.1
Pennington, L.D.2
-
172
-
-
80054736173
-
Enantioselective Total Synthesis of Aplyviolene
-
Schnermann, M. J.; Overman, L. E. Enantioselective Total Synthesis of Aplyviolene J. Am. Chem. Soc. 2011, 133, 16425-16427 10.1021/ja208018s
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 16425-16427
-
-
Schnermann, M.J.1
Overman, L.E.2
-
173
-
-
84866423985
-
A Concise Synthesis of (-)-Aplyviolene Facilitated by a Strategic Tertiary Radical Conjugate Addition
-
Schnermann, M. J.; Overman, L. E. A Concise Synthesis of (-)-Aplyviolene Facilitated by a Strategic Tertiary Radical Conjugate Addition Angew. Chem., Int. Ed. 2012, 51, 9576-9580 10.1002/anie.201204977
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 9576-9580
-
-
Schnermann, M.J.1
Overman, L.E.2
-
174
-
-
84985209719
-
Erste Synthese von (+)-Homofenchon (1,4,4-Trimethylbicyclo[3.2.1] octan-3-on)
-
Kreiser, W.; Below, P. Erste Synthese von (+)-Homofenchon (1,4,4-Trimethylbicyclo[3.2.1] octan-3-on) Liebigs Ann. Chem. 1985, 1985, 203-209 10.1002/jlac.198519850121
-
(1985)
Liebigs Ann. Chem.
, vol.1985
, pp. 203-209
-
-
Kreiser, W.1
Below, P.2
-
175
-
-
84982282551
-
Fragment Coupling with Tertiary Radicals Generated by Visible-Light Photocatalysis
-
Jamison, C. R.; Overman, L. E. Fragment Coupling with Tertiary Radicals Generated by Visible-Light Photocatalysis Acc. Chem. Res. 2016, 49, 1578-1586 10.1021/acs.accounts.6b00284
-
(2016)
Acc. Chem. Res.
, vol.49
, pp. 1578-1586
-
-
Jamison, C.R.1
Overman, L.E.2
-
176
-
-
0033024035
-
Biological Activity of the Labdane Diterpenes
-
Singh, M.; Pal, M.; Sharma, R. P. Biological Activity of the Labdane Diterpenes Planta Med. 1999, 65, 002-008 10.1055/s-1999-13952
-
(1999)
Planta Med.
, vol.65
, pp. 002-008
-
-
Singh, M.1
Pal, M.2
Sharma, R.P.3
-
177
-
-
77957805361
-
Labdane-type diterpenes: Chemistry and biological activity
-
Demetzos, C.; Dimas, K. S. Labdane-type diterpenes: Chemistry and biological activity Stud. Nat. Prod. Chem. 2001, 25, 235-292 10.1016/S1572-5995(01)80009-0
-
(2001)
Stud. Nat. Prod. Chem.
, vol.25
, pp. 235-292
-
-
Demetzos, C.1
Dimas, K.S.2
-
178
-
-
0026015335
-
Dichlorolissoclimide, a New Cytotoxic Labdane Derivative from Lissoclinum voeltzkowi Michaelson (Urochordata)
-
Malochet-Grivois, C.; Cotelle, P.; Biard, J. F.; Hénichart, J. P.; Debitus, C.; Roussakis, C.; Verbist, J.-F. Dichlorolissoclimide, a New Cytotoxic Labdane Derivative from Lissoclinum voeltzkowi Michaelson (Urochordata) Tetrahedron Lett. 1991, 32, 6701-6702 10.1016/S0040-4039(00)93579-2
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 6701-6702
-
-
Malochet-Grivois, C.1
Cotelle, P.2
Biard, J.F.3
Hénichart, J.P.4
Debitus, C.5
Roussakis, C.6
Verbist, J.-F.7
-
179
-
-
0027074330
-
Effects in vitro of two marine substances, chlorolissoclimide and dichlorolissoclimide, on a non-small-cell bronchopulmonary carcinoma line (NSCLC-N6)
-
Malochet-Grivois, C.; Roussakis, C.; Robillard, N.; Biard, J. F.; Riou, D.; Debitus, C.; Verbist, J.-F. Effects in vitro of two marine substances, chlorolissoclimide and dichlorolissoclimide, on a non-small-cell bronchopulmonary carcinoma line (NSCLC-N6) Anti-Cancer Drug Des. 1992, 7, 493-502
-
(1992)
Anti-Cancer Drug Des.
, vol.7
, pp. 493-502
-
-
Malochet-Grivois, C.1
Roussakis, C.2
Robillard, N.3
Biard, J.F.4
Riou, D.5
Debitus, C.6
Verbist, J.-F.7
-
180
-
-
84955439482
-
Site-Selective Aliphatic C-H Chlorination Using N-Chloroamides Enables a Synthesis of Chlorolissoclimide
-
Quinn, R. K.; Könst, Z. A.; Michalak, S. E.; Schmidt, Y.; Szklarski, A. R.; Flores, A. R.; Nam, S.; Horne, D. A.; Vanderwal, C. D.; Alexanian, E. J. Site-Selective Aliphatic C-H Chlorination Using N-Chloroamides Enables a Synthesis of Chlorolissoclimide J. Am. Chem. Soc. 2016, 138, 696-702 10.1021/jacs.5b12308
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 696-702
-
-
Quinn, R.K.1
Könst, Z.A.2
Michalak, S.E.3
Schmidt, Y.4
Szklarski, A.R.5
Flores, A.R.6
Nam, S.7
Horne, D.A.8
Vanderwal, C.D.9
Alexanian, E.J.10
-
181
-
-
0242694922
-
Metal-Free, Selective Alkane Functionalizations
-
Fokin, A. A.; Schreiner, P. R. Metal-Free, Selective Alkane Functionalizations Adv. Synth. Catal. 2003, 345, 1035-1052 10.1002/adsc.200303049
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 1035-1052
-
-
Fokin, A.A.1
Schreiner, P.R.2
-
182
-
-
84908388181
-
Site-Selective Aliphatic C-H Bromination Using N-Bromoamides and Visible Light
-
Schmidt, V. A.; Quinn, R. K.; Brusoe, A. T.; Alexanian, E. J. Site-Selective Aliphatic C-H Bromination Using N-Bromoamides and Visible Light J. Am. Chem. Soc. 2014, 136, 14389-14392 10.1021/ja508469u
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14389-14392
-
-
Schmidt, V.A.1
Quinn, R.K.2
Brusoe, A.T.3
Alexanian, E.J.4
-
183
-
-
71949100419
-
Strain Release in C-H Bond Activation?
-
Chen, K.; Eschenmoser, A.; Baran, P. S. Strain Release in C-H Bond Activation? Angew. Chem., Int. Ed. 2009, 48, 9705-9708 10.1002/anie.200904474
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9705-9708
-
-
Chen, K.1
Eschenmoser, A.2
Baran, P.S.3
-
184
-
-
79953249140
-
If C-H bonds could talk: Selective C-H bond oxidation
-
Newhouse, T.; Baran, P. S. If C-H bonds could talk: selective C-H bond oxidation Angew. Chem., Int. Ed. 2011, 50, 3362-3374 10.1002/anie.201006368
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 3362-3374
-
-
Newhouse, T.1
Baran, P.S.2
-
185
-
-
75749110908
-
Combined Effects on Selectivity in Fe-Catalyzed Methylene Oxidation
-
Chen, M. S.; White, M. C. Combined Effects on Selectivity in Fe-Catalyzed Methylene Oxidation Science 2010, 327, 566-571 10.1126/science.1183602
-
(2010)
Science
, vol.327
, pp. 566-571
-
-
Chen, M.S.1
White, M.C.2
-
186
-
-
84948739332
-
Transition-Metal-Free Oxidative Aliphatic C-H Azidation
-
Zhang, X.; Yang, H.; Tang, P. Transition-Metal-Free Oxidative Aliphatic C-H Azidation Org. Lett. 2015, 17, 5828-5831 10.1021/acs.orglett.5b03001
-
(2015)
Org. Lett.
, vol.17
, pp. 5828-5831
-
-
Zhang, X.1
Yang, H.2
Tang, P.3
-
187
-
-
84928709381
-
Manganese-Catalyzed Late-Stage Aliphatic C-H Azidation
-
Huang, X.; Bergsten, T. M.; Groves, J. T. Manganese-Catalyzed Late-Stage Aliphatic C-H Azidation J. Am. Chem. Soc. 2015, 137, 5300-5303 10.1021/jacs.5b01983
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 5300-5303
-
-
Huang, X.1
Bergsten, T.M.2
Groves, J.T.3
-
188
-
-
84866068267
-
Oxidative Aliphatic C-H Fluorination with Fluoride Ion Catalyzed by a Manganese Porphyrin
-
Liu, W.; Huang, X.; Cheng, M.-J.; Nielsen, R. J.; Goddard, W. A., III; Groves, J. T. Oxidative Aliphatic C-H Fluorination with Fluoride Ion Catalyzed by a Manganese Porphyrin Science 2012, 337, 1322-1325 10.1126/science.1222327
-
(2012)
Science
, vol.337
, pp. 1322-1325
-
-
Liu, W.1
Huang, X.2
Cheng, M.-J.3
Nielsen, R.J.4
Goddard, W.A.5
Groves, J.T.6
-
189
-
-
84903976893
-
Vanadium-Catalyzed C(sp3)-H Fluorination Reactions
-
Xia, J.-B.; Ma, Y.; Chen, C. Vanadium-Catalyzed C(sp3)-H Fluorination Reactions Org. Chem. Front. 2014, 1, 468-472 10.1039/c4qo00057a
-
(2014)
Org. Chem. Front.
, vol.1
, pp. 468-472
-
-
Xia, J.-B.1
Ma, Y.2
Chen, C.3
-
190
-
-
84899650866
-
A Convenient Photocatalytic Fluorination of Unactivated C-H Bonds
-
Halperin, S. D.; Fan, H.; Chang, S.; Martin, R. E.; Britton, R. A Convenient Photocatalytic Fluorination of Unactivated C-H Bonds Angew. Chem., Int. Ed. 2014, 53, 4690-4693 10.1002/anie.201400420
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 4690-4693
-
-
Halperin, S.D.1
Fan, H.2
Chang, S.3
Martin, R.E.4
Britton, R.5
-
191
-
-
84893492645
-
A photocatalyzed aliphatic fluorination
-
Bloom, S.; Knippel, J. L.; Lectka, T. A photocatalyzed aliphatic fluorination Chem. Sci. 2014, 5, 1175-1178 10.1039/c3sc53261e
-
(2014)
Chem. Sci.
, vol.5
, pp. 1175-1178
-
-
Bloom, S.1
Knippel, J.L.2
Lectka, T.3
-
193
-
-
77956634705
-
Manganese Porphyrins Catalyze Selective C-H Bond Halogenations
-
Liu, W.; Groves, J. T. Manganese Porphyrins Catalyze Selective C-H Bond Halogenations J. Am. Chem. Soc. 2010, 132, 12847-12849 10.1021/ja105548x
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 12847-12849
-
-
Liu, W.1
Groves, J.T.2
-
194
-
-
84908893256
-
Selective fluorination of alkyl C-H bonds via photocatalysis
-
Kee, C. W.; Chin, K. F.; Wong, M. W.; Tan, C.-H. Selective fluorination of alkyl C-H bonds via photocatalysis Chem. Commun. 2014, 50, 8211-8214 10.1039/C4CC01848F
-
(2014)
Chem. Commun.
, vol.50
, pp. 8211-8214
-
-
Kee, C.W.1
Chin, K.F.2
Wong, M.W.3
Tan, C.-H.4
-
195
-
-
84939574763
-
Transition-metal free oxidative aliphatic C-H fluorination
-
Zhang, X.; Guo, S.; Tang, P. Transition-metal free oxidative aliphatic C-H fluorination Org. Chem. Front. 2015, 2, 806-810 10.1039/C5QO00095E
-
(2015)
Org. Chem. Front.
, vol.2
, pp. 806-810
-
-
Zhang, X.1
Guo, S.2
Tang, P.3
-
196
-
-
78049238949
-
A fast and straightforward route towards the synthesis of the lissoclimide class of anti-tumour agents
-
Nguyen, T. M.; Vu, N. Q.; Youte, J.-J.; Lau, J.; Cheong, A.; Ho, Y. S.; Tan, B. S. W.; Yoganathan, K.; Butler, M. S.; Chai, C. L. L. A fast and straightforward route towards the synthesis of the lissoclimide class of anti-tumour agents Tetrahedron 2010, 66, 9270-9276 10.1016/j.tet.2010.09.031
-
(2010)
Tetrahedron
, vol.66
, pp. 9270-9276
-
-
Nguyen, T.M.1
Vu, N.Q.2
Youte, J.-J.3
Lau, J.4
Cheong, A.5
Ho, Y.S.6
Tan, B.S.W.7
Yoganathan, K.8
Butler, M.S.9
Chai, C.L.L.10
-
197
-
-
33845280449
-
Synthesis of cembranes and cembranolides
-
Tius, M. A. Synthesis of cembranes and cembranolides Chem. Rev. 1988, 88, 719-732 10.1021/cr00087a001
-
(1988)
Chem. Rev.
, vol.88
, pp. 719-732
-
-
Tius, M.A.1
-
198
-
-
0042752593
-
Cubitene: An Irregular Twelve-Membered-Ring Diterpene from a Termite Soldier
-
Prestwich, G. D.; Wiemer, D. F.; Meinwald, J.; Clardy, J. Cubitene: An Irregular Twelve-Membered-Ring Diterpene from a Termite Soldier J. Am. Chem. Soc. 1978, 100, 2560-2561 10.1021/ja00476a056
-
(1978)
J. Am. Chem. Soc.
, vol.100
, pp. 2560-2561
-
-
Prestwich, G.D.1
Wiemer, D.F.2
Meinwald, J.3
Clardy, J.4
-
199
-
-
0001651497
-
Cembranoids, Pseudopteranoids, and Cubitanoids of Natural Occurrence
-
Herz, W. Kirby, G. W. Moore, R. E. Steglich, W. Tamm, C. Springer: New York
-
Wahlberg, I.; Eklund, A.-M. Cembranoids, Pseudopteranoids, and Cubitanoids of Natural Occurrence. In Progress in the Chemistry of Organic Natural Products; Herz, W.; Kirby, G. W.; Moore, R. E.; Steglich, W.; Tamm, C., Eds.; Springer: New York, 1992; pp 142-294.
-
(1992)
Progress in the Chemistry of Organic Natural Products
, pp. 142-294
-
-
Wahlberg, I.1
Eklund, A.-M.2
-
200
-
-
79958832724
-
A Concise, Stereocontrolled Total Synthesis of Rippertenol
-
Snyder, S. A.; Wespe, D. A.; von Hof, J. M. A Concise, Stereocontrolled Total Synthesis of Rippertenol J. Am. Chem. Soc. 2011, 133, 8850-8853 10.1021/ja202859f
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 8850-8853
-
-
Snyder, S.A.1
Wespe, D.A.2
Von Hof, J.M.3
-
201
-
-
76849083416
-
-
Vig, O. P.; Bari, S. S.; Trehan, I. R.; Vig, R. Indian J. Chem., Sect. B 1980, 446-449
-
(1980)
Indian J. Chem., Sect. B
, pp. 446-449
-
-
Vig, O.P.1
Bari, S.S.2
Trehan, I.R.3
Vig, R.4
-
202
-
-
0010329437
-
Synthesis of Macrocyclic Terpenoids by Intramolecular Cyclization VII. Total Synthesis of (±)-cubitene
-
Kodama, M.; Takahashi, T.; Kojima, T.; Itô, S. Synthesis of Macrocyclic Terpenoids by Intramolecular Cyclization VII. Total Synthesis of (±)-cubitene Tetrahedron Lett. 1982, 23, 3397-3400 10.1016/S0040-4039(00)87625-X
-
(1982)
Tetrahedron Lett.
, vol.23
, pp. 3397-3400
-
-
Kodama, M.1
Takahashi, T.2
Kojima, T.3
Itô, S.4
-
203
-
-
0030363064
-
Enantioselective Synthesis and Absolute Configuration of (+)-Cubitene
-
Kodama, M.; Maeda, H.; Hioki, H. Enantioselective Synthesis and Absolute Configuration of (+)-Cubitene Chem. Lett. 1996, 25, 809-810 10.1246/cl.1996.809
-
(1996)
Chem. Lett.
, vol.25
, pp. 809-810
-
-
Kodama, M.1
Maeda, H.2
Hioki, H.3
-
204
-
-
84867535755
-
Enantioselective Total Synthesis of the Diterpene (+)-Cubitene
-
Simon, K.; Wefer, J.; Schöttner, E.; Lindel, T. Enantioselective Total Synthesis of the Diterpene (+)-Cubitene Angew. Chem., Int. Ed. 2012, 51, 10889-10892 10.1002/anie.201205143
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 10889-10892
-
-
Simon, K.1
Wefer, J.2
Schöttner, E.3
Lindel, T.4
-
205
-
-
76849104501
-
Enantiospecific Synthesis of the Cubitane Skeleton
-
Schöttner, E.; Wiechoczek, M.; Jones, P. G.; Lindel, T. Enantiospecific Synthesis of the Cubitane Skeleton Org. Lett. 2010, 12, 784-787 10.1021/ol902854t
-
(2010)
Org. Lett.
, vol.12
, pp. 784-787
-
-
Schöttner, E.1
Wiechoczek, M.2
Jones, P.G.3
Lindel, T.4
-
207
-
-
20344394459
-
Vigulariol, a New Metabolite from the Sea Pen Vigularia juncea
-
Su, J.-H.; Huang, H.-C.; Chao, C.-H.; Yan, L.-Y.; Wu, Y.-C.; Sheu, J.-H.; Wu, C.-C. Vigulariol, a New Metabolite from the Sea Pen Vigularia juncea Bull. Chem. Soc. Jpn. 2005, 78, 877-879 10.1246/bcsj.78.877
-
(2005)
Bull. Chem. Soc. Jpn.
, vol.78
, pp. 877-879
-
-
Su, J.-H.1
Huang, H.-C.2
Chao, C.-H.3
Yan, L.-Y.4
Wu, Y.-C.5
Sheu, J.-H.6
Wu, C.-C.7
-
208
-
-
0036727043
-
The Heterocyclic Natural Products of Gorgonian Corals of Genus Briareum Exclusive of Briarane-Type Diterpenoids
-
Sung, P.-J.; Chen, M.-C. The Heterocyclic Natural Products of Gorgonian Corals of Genus Briareum Exclusive of Briarane-Type Diterpenoids Heterocycles 2002, 57, 1705-1715 10.3987/REV-02-553
-
(2002)
Heterocycles
, vol.57
, pp. 1705-1715
-
-
Sung, P.-J.1
Chen, M.-C.2
-
209
-
-
80055097831
-
The 2,11-Cyclized Cembranoids: Cladiellins, Asbestinins, and Briarellins (Period 1998-2010)
-
Welford, A. J.; Collins, I. The 2,11-Cyclized Cembranoids: Cladiellins, Asbestinins, and Briarellins (Period 1998-2010) J. Nat. Prod. 2011, 74, 2318-2328 10.1021/np200125v
-
(2011)
J. Nat. Prod.
, vol.74
, pp. 2318-2328
-
-
Welford, A.J.1
Collins, I.2
-
210
-
-
61949398187
-
Strategies for the Total Synthesis of C2-C11 Cyclized Cembranoids
-
Ellis, J. M.; Crimmins, M. T. Strategies for the Total Synthesis of C2-C11 Cyclized Cembranoids Chem. Rev. 2008, 108, 5278-5298 10.1021/cr078117u
-
(2008)
Chem. Rev.
, vol.108
, pp. 5278-5298
-
-
Ellis, J.M.1
Crimmins, M.T.2
-
211
-
-
0035913732
-
Total Asymmetric Synthesis of the Putative Structure of the Cytotoxic Diterpenoid (-)-Sclerophytin A and of the Authentic Natural Sclerophytins A and B
-
Bernardelli, P.; Moradei, O. M.; Friedrich, D.; Yang, J.; Gallou, F.; Dyck, B. P.; Doskotch, R. W.; Lange, T.; Paquette, L. A. Total Asymmetric Synthesis of the Putative Structure of the Cytotoxic Diterpenoid (-)-Sclerophytin A and of the Authentic Natural Sclerophytins A and B J. Am. Chem. Soc. 2001, 123, 9021-9032 10.1021/ja011285y
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9021-9032
-
-
Bernardelli, P.1
Moradei, O.M.2
Friedrich, D.3
Yang, J.4
Gallou, F.5
Dyck, B.P.6
Doskotch, R.W.7
Lange, T.8
Paquette, L.A.9
-
212
-
-
33846448716
-
A Concise Total Synthesis of (±)-Vigulariol
-
Clark, J. S.; Hayes, S. T.; Wilson, C.; Gobbi, L. A Concise Total Synthesis of (±)-Vigulariol Angew. Chem., Int. Ed. 2007, 46, 437-440 10.1002/anie.200603880
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 437-440
-
-
Clark, J.S.1
Hayes, S.T.2
Wilson, C.3
Gobbi, L.4
-
213
-
-
41049115005
-
Asymmetric Total Synthesis and X-Ray Crystal Structure of the Cytotoxic Marine Diterpene (+)-Vigulariol
-
Becker, J.; Bergander, K.; Fröhlich, R.; Hoppe, D. Asymmetric Total Synthesis and X-Ray Crystal Structure of the Cytotoxic Marine Diterpene (+)-Vigulariol Angew. Chem., Int. Ed. 2008, 47, 1654-1657 10.1002/anie.200704678
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 1654-1657
-
-
Becker, J.1
Bergander, K.2
Fröhlich, R.3
Hoppe, D.4
-
214
-
-
80052782155
-
Total Syntheses of (+)-Vigulariol and (-)-Sclerophytin A
-
Crimmins, M. T.; Stauffer, C. S.; Mans, M. C. Total Syntheses of (+)-Vigulariol and (-)-Sclerophytin A Org. Lett. 2011, 13, 4890-4893 10.1021/ol201981j
-
(2011)
Org. Lett.
, vol.13
, pp. 4890-4893
-
-
Crimmins, M.T.1
Stauffer, C.S.2
Mans, M.C.3
-
215
-
-
67349149964
-
Total synthesis of eudesmane terpenes by site-selective C-H oxidations
-
Chen, K.; Baran, P. S. Total synthesis of eudesmane terpenes by site-selective C-H oxidations Nature 2009, 459, 824-828 10.1038/nature08043
-
(2009)
Nature
, vol.459
, pp. 824-828
-
-
Chen, K.1
Baran, P.S.2
-
216
-
-
27544464237
-
Diastereoselective Synthesis of Enantioenriched, Annulated Tetrahydrofurans by Simultaneous Formation of the O-1-C-5 and the C-5-C-4 bonds
-
Ünaldi, S.; Özlügedik, M.; Fröhlich, R.; Hoppe, D. Diastereoselective Synthesis of Enantioenriched, Annulated Tetrahydrofurans by Simultaneous Formation of the O-1-C-5 and the C-5-C-4 bonds Adv. Synth. Catal. 2005, 347, 1621-1626 10.1002/adsc.200505142
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1621-1626
-
-
Ünaldi, S.1
Özlügedik, M.2
Fröhlich, R.3
Hoppe, D.4
-
217
-
-
0142174551
-
-
Hodgson, D. M. Springer: Heidelberg
-
Hoppe, D.; Marr, F.; Brüggemann, M. In Organolithiums in Enantioselective Synthesis; Hodgson, D. M., Ed.; Springer: Heidelberg, 2003; pp 61-137.
-
(2003)
Organolithiums in Enantioselective Synthesis
, pp. 61-137
-
-
Hoppe, D.1
Marr, F.2
Brüggemann, M.3
-
218
-
-
0037503118
-
-
Rappoport, Z. Marek, I. Wiley: Chichester
-
Hoppe, D.; Christoph, G. In The Chemistry of Organolithium Compounds; Rappoport, Z.; Marek, I., Eds.; Wiley: Chichester, 2004; p 1055.
-
(2004)
The Chemistry of Organolithium Compounds
, pp. 1055
-
-
Hoppe, D.1
Christoph, G.2
-
219
-
-
33947440814
-
Plant insecticides I. Ryanodine, a new alkaloid from Ryania speciosa Vahl
-
Rogers, E. F.; Koniuszy, F. R.; Shavel, J.; Folkers, K. Plant insecticides I. Ryanodine, a new alkaloid from Ryania speciosa Vahl J. Am. Chem. Soc. 1948, 70, 3086-3088 10.1021/ja01189a074
-
(1948)
J. Am. Chem. Soc.
, vol.70
, pp. 3086-3088
-
-
Rogers, E.F.1
Koniuszy, F.R.2
Shavel, J.3
Folkers, K.4
-
220
-
-
0005980724
-
The structure of ryanodine
-
Wiesner, K.; Valenta, Z.; Findlay, J. A. The structure of ryanodine Tetrahedron Lett. 1967, 8, 221-223 10.1016/S0040-4039(00)90521-5
-
(1967)
Tetrahedron Lett.
, vol.8
, pp. 221-223
-
-
Wiesner, K.1
Valenta, Z.2
Findlay, J.A.3
-
221
-
-
1542593711
-
The molecular structure of ryanodol-p-bromo benzyl ether
-
Srivastava, S. N.; Przybylska, M. The molecular structure of ryanodol-p-bromo benzyl ether Can. J. Chem. 1968, 46, 795-797 10.1139/v68-133
-
(1968)
Can. J. Chem.
, vol.46
, pp. 795-797
-
-
Srivastava, S.N.1
Przybylska, M.2
-
222
-
-
0022395442
-
The calcium-ryanodine receptor complex of skeletal and cardiac muscle
-
Pessah, I. N.; Waterhouse, A. L.; Casida, J. E. The calcium-ryanodine receptor complex of skeletal and cardiac muscle Biochem. Biophys. Res. Commun. 1985, 128, 449-456 10.1016/0006-291X(85)91699-7
-
(1985)
Biochem. Biophys. Res. Commun.
, vol.128
, pp. 449-456
-
-
Pessah, I.N.1
Waterhouse, A.L.2
Casida, J.E.3
-
223
-
-
79952478406
-
Ryanodine receptors: Structure, expression, molecular details, and function in calcium release
-
Lanner, J. T.; Georgiou, D. K.; Joshi, A. D.; Hamilton, S. L. Ryanodine receptors: structure, expression, molecular details, and function in calcium release Cold Spring Harbor Perspect. Biol. 2010, 2, a003996 10.1101/cshperspect.a003996
-
(2010)
Cold Spring Harbor Perspect. Biol.
, vol.2
, pp. a003996
-
-
Lanner, J.T.1
Georgiou, D.K.2
Joshi, A.D.3
Hamilton, S.L.4
-
224
-
-
0023202869
-
Structural aspects of ryanodine action and selectivity
-
Waterhouse, A. L.; Pessah, I. N.; Francini, A. O.; Casida, J. E. Structural aspects of ryanodine action and selectivity J. Med. Chem. 1987, 30, 710-716 10.1021/jm00387a022
-
(1987)
J. Med. Chem.
, vol.30
, pp. 710-716
-
-
Waterhouse, A.L.1
Pessah, I.N.2
Francini, A.O.3
Casida, J.E.4
-
225
-
-
0028227183
-
Structural determinants of high-affinity binding of ryanoids to the vertebrate skeletal muscle ryanodine receptor: A comparative molecular field analysis
-
Welch, W.; Ahmad, S.; Airey, J. A.; Gerzon, K.; Humerickhouse, R. A.; Besch, H. R.; Ruest, L.; Deslongchamps, P.; Sutko, J. L. Structural determinants of high-affinity binding of ryanoids to the vertebrate skeletal muscle ryanodine receptor: A comparative molecular field analysis Biochemistry 1994, 33, 6074-6085 10.1021/bi00186a006
-
(1994)
Biochemistry
, vol.33
, pp. 6074-6085
-
-
Welch, W.1
Ahmad, S.2
Airey, J.A.3
Gerzon, K.4
Humerickhouse, R.A.5
Besch, H.R.6
Ruest, L.7
Deslongchamps, P.8
Sutko, J.L.9
-
226
-
-
0030893595
-
The pharmacology of ryanodine and related compounds
-
Sutko, J. L.; Airey, J. A.; Welch, W.; Ruest, L. The pharmacology of ryanodine and related compounds Pharmacol. Rev. 1997, 49, 53-98
-
(1997)
Pharmacol. Rev.
, vol.49
, pp. 53-98
-
-
Sutko, J.L.1
Airey, J.A.2
Welch, W.3
Ruest, L.4
-
227
-
-
0000623741
-
Total synthesis of ryanodol
-
Bélanger, A.; Berney, D. J. F.; Borschberg, H.-J.; Brousseau, R.; Doutheau, A.; Durand, R.; Katayama, H.; Lapalme, R.; Leturc, D. M.; Liao, C.-C. et al. Total synthesis of ryanodol Can. J. Chem. 1979, 57, 3348-3354 10.1139/v79-547
-
(1979)
Can. J. Chem.
, vol.57
, pp. 3348-3354
-
-
Bélanger, A.1
Berney, D.J.F.2
Borschberg, H.-J.3
Brousseau, R.4
Doutheau, A.5
Durand, R.6
Katayama, H.7
Lapalme, R.8
Leturc, D.M.9
Liao, C.-C.10
-
228
-
-
0025214273
-
The total synthesis of (+)-ryanodol. Part I. General strategy and search for a convenient diene for the construction of a key tricyclic intermediate
-
Deslongchamps, P.; Bélanger, A.; Berney, D. J. F.; Borschberg, H.-J.; Brousseau, R.; Doutheau, A.; Durand, R.; Katayama, H.; Lapalme, R.; Leturc, D. M. et al. The total synthesis of (+)-ryanodol. Part I. General strategy and search for a convenient diene for the construction of a key tricyclic intermediate Can. J. Chem. 1990, 68, 115-126 10.1139/v90-021
-
(1990)
Can. J. Chem.
, vol.68
, pp. 115-126
-
-
Deslongchamps, P.1
Bélanger, A.2
Berney, D.J.F.3
Borschberg, H.-J.4
Brousseau, R.5
Doutheau, A.6
Durand, R.7
Katayama, H.8
Lapalme, R.9
Leturc, D.M.10
-
229
-
-
0025219656
-
The total synthesis of (+)-ryanodol. Part II. Model studies for rings B and C and of (+)-anhydroryanodol. Preparation of a key pentacyclic intermediate
-
Deslongchamps, P.; Bélanger, A.; Berney, D. J. F.; Borschberg, H.-J.; Brousseau, R.; Doutheau, A.; Durand, R.; Katayama, H.; Lapalme, R.; Leturc, D. M. et al. The total synthesis of (+)-ryanodol. Part II. Model studies for rings B and C and of (+)-anhydroryanodol. Preparation of a key pentacyclic intermediate Can. J. Chem. 1990, 68, 127-152 10.1139/v90-022
-
(1990)
Can. J. Chem.
, vol.68
, pp. 127-152
-
-
Deslongchamps, P.1
Bélanger, A.2
Berney, D.J.F.3
Borschberg, H.-J.4
Brousseau, R.5
Doutheau, A.6
Durand, R.7
Katayama, H.8
Lapalme, R.9
Leturc, D.M.10
-
230
-
-
0025232665
-
The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate
-
Deslongchamps, P.; Bélanger, A.; Berney, D. J. F.; Borschberg, H.-J.; Brousseau, R.; Doutheau, A.; Durand, R.; Katayama, H.; Lapalme, R.; Leturc, D. M. et al. The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate Can. J. Chem. 1990, 68, 153-185 10.1139/v90-023
-
(1990)
Can. J. Chem.
, vol.68
, pp. 153-185
-
-
Deslongchamps, P.1
Bélanger, A.2
Berney, D.J.F.3
Borschberg, H.-J.4
Brousseau, R.5
Doutheau, A.6
Durand, R.7
Katayama, H.8
Lapalme, R.9
Leturc, D.M.10
-
231
-
-
0025254089
-
The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol
-
Deslongchamps, P.; Bélanger, A.; Berney, D. J. F.; Borschberg, H.-J.; Brousseau, R.; Doutheau, A.; Durand, R.; Katayama, H.; Lapalme, R.; Leturc, D. M. et al. The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol Can. J. Chem. 1990, 68, 186-192 10.1139/v90-024
-
(1990)
Can. J. Chem.
, vol.68
, pp. 186-192
-
-
Deslongchamps, P.1
Bélanger, A.2
Berney, D.J.F.3
Borschberg, H.-J.4
Brousseau, R.5
Doutheau, A.6
Durand, R.7
Katayama, H.8
Lapalme, R.9
Leturc, D.M.10
-
232
-
-
84899580834
-
Total synthesis of ryanodol
-
Nagatomo, M.; Koshimizu, M.; Masuda, K.; Tabuchi, T.; Urabe, D.; Inoue, M. Total synthesis of ryanodol J. Am. Chem. Soc. 2014, 136, 5916-5919 10.1021/ja502770n
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5916-5919
-
-
Nagatomo, M.1
Koshimizu, M.2
Masuda, K.3
Tabuchi, T.4
Urabe, D.5
Inoue, M.6
-
233
-
-
84984908039
-
A 15-step synthesis of (+)-ryanodol
-
Chuang, K. V.; Xu, C.; Reisman, S. E. A 15-step synthesis of (+)-ryanodol Science 2016, 353, 912-915 10.1126/science.aag1028
-
(2016)
Science
, vol.353
, pp. 912-915
-
-
Chuang, K.V.1
Xu, C.2
Reisman, S.E.3
-
234
-
-
84954357113
-
Symmetry-driven strategy for the assembly of the core tetracycle of (+)-ryanodine: Synthetic utility of a cobalt-catalyzed olefin oxidation and α-alkoxy bridgehead radical reaction
-
Nagatomo, M.; Hagiwara, K.; Masuda, K.; Koshimizu, M.; Kawamata, T.; Matsui, Y.; Urabe, D.; Inoue, M. Symmetry-driven strategy for the assembly of the core tetracycle of (+)-ryanodine: Synthetic utility of a cobalt-catalyzed olefin oxidation and α-alkoxy bridgehead radical reaction Chem.-Eur. J. 2016, 22, 222-229 10.1002/chem.201503640
-
(2016)
Chem. - Eur. J.
, vol.22
, pp. 222-229
-
-
Nagatomo, M.1
Hagiwara, K.2
Masuda, K.3
Koshimizu, M.4
Kawamata, T.5
Matsui, Y.6
Urabe, D.7
Inoue, M.8
-
235
-
-
84954317506
-
Asymmetric total synthesis of (+)-ryanodol and (+)-ryanodine
-
Masuda, K.; Koshimizu, M.; Nagatomo, M.; Inoue, M. Asymmetric total synthesis of (+)-ryanodol and (+)-ryanodine Chem.-Eur. J. 2016, 22, 230-236 10.1002/chem.201503641
-
(2016)
Chem. - Eur. J.
, vol.22
, pp. 230-236
-
-
Masuda, K.1
Koshimizu, M.2
Nagatomo, M.3
Inoue, M.4
-
236
-
-
84882808258
-
Efficient intramolecular cyclizations of phenoxyethynyl diols into multisubstituted α,β-unsaturated lactones
-
Egi, M.; Ota, Y.; Nishimura, Y.; Shimizu, K.; Azechi, K.; Akai, S. Efficient intramolecular cyclizations of phenoxyethynyl diols into multisubstituted α,β-unsaturated lactones Org. Lett. 2013, 15, 4150-4153 10.1021/ol401824v
-
(2013)
Org. Lett.
, vol.15
, pp. 4150-4153
-
-
Egi, M.1
Ota, Y.2
Nishimura, Y.3
Shimizu, K.4
Azechi, K.5
Akai, S.6
-
237
-
-
0032360438
-
Rhodium-catalyzed intramolecular Pauson-Khand reaction
-
Koga, Y.; Kobayashi, T.; Narasaka, K. Rhodium-catalyzed intramolecular Pauson-Khand reaction Chem. Lett. 1998, 27, 249-250 10.1246/cl.1998.249
-
(1998)
Chem. Lett.
, vol.27
, pp. 249-250
-
-
Koga, Y.1
Kobayashi, T.2
Narasaka, K.3
-
238
-
-
0026721571
-
The synthesis of carbocyclic eight-membered rings
-
Petasis, N. A.; Patane, M. A. The synthesis of carbocyclic eight-membered rings Tetrahedron 1992, 48, 5757-5821 10.1016/S0040-4020(01)90172-3
-
(1992)
Tetrahedron
, vol.48
, pp. 5757-5821
-
-
Petasis, N.A.1
Patane, M.A.2
-
239
-
-
0031081679
-
Fusicoccin - A key to multiple 14-3-3 locks?
-
DeBoer, B. Fusicoccin-a key to multiple 14-3-3 locks? Trends Plant Sci. 1997, 2, 60-66 10.1016/S1360-1385(97)82564-2
-
(1997)
Trends Plant Sci.
, vol.2
, pp. 60-66
-
-
DeBoer, B.1
-
240
-
-
0031590284
-
Cotylenin A, a Plant-Growth Regulator, Induces the Differentiation in Murine and Human Myeloid Leukemia Cells
-
Asahi, K.; Honma, Y.; Hazeki, K.; Sassa, T.; Kubohara, Y.; Sakurai, A.; Takahashi, N. Cotylenin A, a Plant-Growth Regulator, Induces the Differentiation in Murine and Human Myeloid Leukemia Cells Biochem. Biophys. Res. Commun. 1997, 238, 758-763 10.1006/bbrc.1997.7385
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.238
, pp. 758-763
-
-
Asahi, K.1
Honma, Y.2
Hazeki, K.3
Sassa, T.4
Kubohara, Y.5
Sakurai, A.6
Takahashi, N.7
-
241
-
-
84861886597
-
Fusicoccanes: Diterpenes with surprising biological functions
-
De Boer, A. H.; de Vries-Van Leeuwen, I. J. Fusicoccanes: diterpenes with surprising biological functions Trends Plant Sci. 2012, 17, 360-368 10.1016/j.tplants.2012.02.007
-
(2012)
Trends Plant Sci.
, vol.17
, pp. 360-368
-
-
De Boer, A.H.1
De Vries-Van Leeuwen, I.J.2
-
242
-
-
0002654035
-
Total Synthesis of (-)-Cotylenol, a Fungal Metabolite Having a Leaf Growth Activity
-
Okamoto, H.; Arita, H.; Kato, N.; Takeshita, H. Total Synthesis of (-)-Cotylenol, a Fungal Metabolite Having a Leaf Growth Activity Chem. Lett. 1994, 23, 2335-2338 10.1246/cl.1994.2335
-
(1994)
Chem. Lett.
, vol.23
, pp. 2335-2338
-
-
Okamoto, H.1
Arita, H.2
Kato, N.3
Takeshita, H.4
-
243
-
-
0029930377
-
Total Synthesis of (-)-Cotylenol, a Fungal Metabolite Having a Leaf Growth Activity
-
Kato, N.; Okamoto, H.; Takeshita, H. Total Synthesis of (-)-Cotylenol, a Fungal Metabolite Having a Leaf Growth Activity Tetrahedron 1996, 52, 3921-3932 10.1016/S0040-4020(96)00059-2
-
(1996)
Tetrahedron
, vol.52
, pp. 3921-3932
-
-
Kato, N.1
Okamoto, H.2
Takeshita, H.3
-
244
-
-
0030826214
-
Total Synthesis of (+)-Epoxydictymene. Application of Alkoxy-Directed Cyclization to Diterpenoid Construction
-
Paquette, L. A.; Sun, L.-Q.; Friedrich, D.; Savage, P. B. Total Synthesis of (+)-Epoxydictymene. Application of Alkoxy-Directed Cyclization to Diterpenoid Construction J. Am. Chem. Soc. 1997, 119, 8438-8450 10.1021/ja971526v
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 8438-8450
-
-
Paquette, L.A.1
Sun, L.-Q.2
Friedrich, D.3
Savage, P.B.4
-
245
-
-
0028107984
-
Cobalt-Mediated Total Synthesis of (+)-Epoxydictymene
-
Jamison, T. F.; Shambayati, S.; Crowe, W. E.; Schreiber, S. L. Cobalt-Mediated Total Synthesis of (+)-Epoxydictymene J. Am. Chem. Soc. 1994, 116, 5505-5506 10.1021/ja00091a079
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 5505-5506
-
-
Jamison, T.F.1
Shambayati, S.2
Crowe, W.E.3
Schreiber, S.L.4
-
246
-
-
33846699839
-
Strategies for the Synthesis of Fusicoccanes by Nazarov Reaction of Dolabelladienones: Total Synthesis of (+)-Fusicoauritone
-
Williams, D. R.; Robinson, L. A.; Nevill, C. R.; Reddy, J. P. Strategies for the Synthesis of Fusicoccanes by Nazarov Reaction of Dolabelladienones: Total Synthesis of (+)-Fusicoauritone Angew. Chem., Int. Ed. 2007, 46, 915-918 10.1002/anie.200603853
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 915-918
-
-
Williams, D.R.1
Robinson, L.A.2
Nevill, C.R.3
Reddy, J.P.4
-
247
-
-
0028002692
-
Sphenolobane and fusicoccane diterpenoids from the liverword Anastrophyllum auritum
-
Zapp, J.; Burkhardt, G.; Becker, H. Sphenolobane and fusicoccane diterpenoids from the liverword Anastrophyllum auritum Phytochemistry 1994, 37, 787-793 10.1016/S0031-9422(00)90359-5
-
(1994)
Phytochemistry
, vol.37
, pp. 787-793
-
-
Zapp, J.1
Burkhardt, G.2
Becker, H.3
-
248
-
-
84873391260
-
Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus
-
Chiba, R.; Minami, A.; Gomi, K.; Oikawa, H. Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus Org. Lett. 2013, 15, 594-597 10.1021/ol303408a
-
(2013)
Org. Lett.
, vol.15
, pp. 594-597
-
-
Chiba, R.1
Minami, A.2
Gomi, K.3
Oikawa, H.4
-
249
-
-
0001691069
-
Spiroannelation via intramolecular ketocarbenoid addition. Stereocontrolled synthesis of (-)-acorenone B and (±)-alpha-chamigrene
-
White, J. D.; Ruppert, J. F.; Avery, A.; Torii, S.; Nokami, J. Spiroannelation via intramolecular ketocarbenoid addition. Stereocontrolled synthesis of (-)-acorenone B and (±)-alpha-chamigrene J. Am. Chem. Soc. 1981, 103, 1813-1821 10.1021/ja00397a040
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 1813-1821
-
-
White, J.D.1
Ruppert, J.F.2
Avery, A.3
Torii, S.4
Nokami, J.5
-
250
-
-
0028798174
-
Studies on the Dolabellanes: Stereoselective Transannular Cyclizations of Dolabelladiene Macrocycles
-
Williams, D. R.; Coleman, P. J. Studies on the Dolabellanes: Stereoselective Transannular Cyclizations of Dolabelladiene Macrocycles Tetrahedron Lett. 1995, 36, 39-42 10.1016/0040-4039(94)02164-7
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 39-42
-
-
Williams, D.R.1
Coleman, P.J.2
-
252
-
-
81355123306
-
Lessons and revelations from biomimetic syntheses
-
Razzak, M.; De Brabander, J. K. Lessons and revelations from biomimetic syntheses Nat. Chem. Biol. 2011, 7, 865-875 10.1038/nchembio.709
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 865-875
-
-
Razzak, M.1
De Brabander, J.K.2
-
253
-
-
41749104435
-
Recent advances in biomimetic natural product synthesis
-
Bulger, P. G.; Bagal, S. K.; Marquez, R. Recent advances in biomimetic natural product synthesis Nat. Prod. Rep. 2008, 25, 254-297 10.1039/b705909b
-
(2008)
Nat. Prod. Rep.
, vol.25
, pp. 254-297
-
-
Bulger, P.G.1
Bagal, S.K.2
Marquez, R.3
-
254
-
-
33750574345
-
Biomimetic cyclizations of functionalized isoprenoid polyenes: A cornucopia of synthetic opportunities
-
Brunoldi, E.; Luparia, M.; Porta, A.; Zanoni, G.; Vidari, G. Biomimetic cyclizations of functionalized isoprenoid polyenes: a cornucopia of synthetic opportunities Curr. Org. Chem. 2006, 10, 2259-2282 10.2174/138527206778742614
-
(2006)
Curr. Org. Chem.
, vol.10
, pp. 2259-2282
-
-
Brunoldi, E.1
Luparia, M.2
Porta, A.3
Zanoni, G.4
Vidari, G.5
-
255
-
-
0345862320
-
Comments on recent achievements in biomimetic organic synthesis
-
de la Torre, M. C.; Sierra, M. A. Comments on recent achievements in biomimetic organic synthesis Angew. Chem., Int. Ed. 2004, 43, 160-181 10.1002/anie.200200545
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 160-181
-
-
De La Torre, M.C.1
Sierra, M.A.2
-
256
-
-
70350519149
-
[3,3]-Sigmatropic rearrangements: Recent applications in the total synthesis of natural products
-
Ilardi, E. A.; Stivala, C. E.; Zakarian, A. [3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products Chem. Soc. Rev. 2009, 38, 3133-3148 10.1039/b901177n
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3133-3148
-
-
Ilardi, E.A.1
Stivala, C.E.2
Zakarian, A.3
-
257
-
-
84880136270
-
The Claisen rearrangement in the syntheses of bioactive natural products
-
Majumdar, K. C.; Nandi, R. K. The Claisen rearrangement in the syntheses of bioactive natural products Tetrahedron 2013, 69, 6921-6957 10.1016/j.tet.2013.06.003
-
(2013)
Tetrahedron
, vol.69
, pp. 6921-6957
-
-
Majumdar, K.C.1
Nandi, R.K.2
-
258
-
-
84899978340
-
The Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates - Recent Advances
-
Fernandes, R. A.; Chowdhury, A. K.; Kattanguru, P. The Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates-Recent Advances Eur. J. Org. Chem. 2014, 2014, 2833-2871 10.1002/ejoc.201301033
-
(2014)
Eur. J. Org. Chem.
, vol.2014
, pp. 2833-2871
-
-
Fernandes, R.A.1
Chowdhury, A.K.2
Kattanguru, P.3
-
259
-
-
54849439280
-
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
-
Shi, Q.-W.; Su, X.-H.; Kiyota, H. Chemical and Pharmacological Research of the Plants in Genus Euphorbia Chem. Rev. 2008, 108, 4295-4327 10.1021/cr078350s
-
(2008)
Chem. Rev.
, vol.108
, pp. 4295-4327
-
-
Shi, Q.-W.1
Su, X.-H.2
Kiyota, H.3
-
260
-
-
84921450307
-
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008-2012)
-
Vasas, A.; Hohmann, J. Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008-2012) Chem. Rev. 2014, 114, 8579-8612 10.1021/cr400541j
-
(2014)
Chem. Rev.
, vol.114
, pp. 8579-8612
-
-
Vasas, A.1
Hohmann, J.2
-
261
-
-
0002040960
-
Diterpenoid Irritants and Cocarcinogens in Euphorbiaceae and Thymelacaceae: Structural Relationships in View of their Biogenesis
-
Adolf, W.; Hecker, E. Diterpenoid Irritants and Cocarcinogens in Euphorbiaceae and Thymelacaceae: Structural Relationships in View of their Biogenesis Isr. J. Chem. 1977, 16, 75-83 10.1002/ijch.197700015
-
(1977)
Isr. J. Chem.
, vol.16
, pp. 75-83
-
-
Adolf, W.1
Hecker, E.2
-
262
-
-
65249145156
-
Plant Orthoesters
-
Liao, S.-G.; Chen, H.-D.; Yue, J.-M. Plant Orthoesters Chem. Rev. 2009, 109, 1092-1140 10.1021/cr0782832
-
(2009)
Chem. Rev.
, vol.109
, pp. 1092-1140
-
-
Liao, S.-G.1
Chen, H.-D.2
Yue, J.-M.3
-
263
-
-
0035413601
-
Protein Kinase C: Structural and Spatial Regulation by Phosphorylation, Cofactors, and Macromolecular Interactions
-
Newton, A. C. Protein Kinase C: Structural and Spatial Regulation by Phosphorylation, Cofactors, and Macromolecular Interactions Chem. Rev. 2001, 101, 2353-2364 10.1021/cr0002801
-
(2001)
Chem. Rev.
, vol.101
, pp. 2353-2364
-
-
Newton, A.C.1
-
264
-
-
38349023182
-
Painful toxins acting at TRPV1
-
Cromer, B. A.; McIntyre, P. Painful toxins acting at TRPV1 Toxicon 2008, 51, 163-173 10.1016/j.toxicon.2007.10.012
-
(2008)
Toxicon
, vol.51
, pp. 163-173
-
-
Cromer, B.A.1
McIntyre, P.2
-
265
-
-
0014353314
-
Cocarcinogenic Principles from the Seed Oil of Croton tiglium and from Other Euphorbiaceae
-
Hecker, E. Cocarcinogenic Principles from the Seed Oil of Croton tiglium and from Other Euphorbiaceae Cancer Res. 1968, 28, 2338-2349
-
(1968)
Cancer Res.
, vol.28
, pp. 2338-2349
-
-
Hecker, E.1
-
266
-
-
12344290175
-
Antitumor activity of 3-ingenyl angelate: Plasma membrane and mitochondrial disruption and necrotic cell death
-
Ogbourne, S. M.; Suhrbier, A.; Jones, B.; Cozzi, S. J.; Boyle, G. M.; Morris, M.; McAlpine, D.; Johns, J.; Scott, T. M.; Sutherland, K. P. et al. Antitumor activity of 3-ingenyl angelate: Plasma membrane and mitochondrial disruption and necrotic cell death Cancer Res. 2004, 64, 2833-2839 10.1158/0008-5472.CAN-03-2837
-
(2004)
Cancer Res.
, vol.64
, pp. 2833-2839
-
-
Ogbourne, S.M.1
Suhrbier, A.2
Jones, B.3
Cozzi, S.J.4
Boyle, G.M.5
Morris, M.6
McAlpine, D.7
Johns, J.8
Scott, T.M.9
Sutherland, K.P.10
-
267
-
-
0030044459
-
Mechanism of selective inhibition of human immunodeficiency virus by ingenol triacetate
-
Fujiwara, M.; Ijichi, K.; Tokuhisa, K.; Katsuura, K.; Shigeta, S.; Konno, K.; Wang, G. Y.; Uemura, D.; Yokota, T.; Baba, M. Mechanism of selective inhibition of human immunodeficiency virus by ingenol triacetate Antimicrob. Agents Chemother. 1996, 40, 271-273
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 271-273
-
-
Fujiwara, M.1
Ijichi, K.2
Tokuhisa, K.3
Katsuura, K.4
Shigeta, S.5
Konno, K.6
Wang, G.Y.7
Uemura, D.8
Yokota, T.9
Baba, M.10
-
268
-
-
0026518042
-
Specific binding to protein kinase C by ingenol and its induction of biological responses
-
Hasler, C. M.; Acs, G.; Blumberg, P. M. Specific binding to protein kinase C by ingenol and its induction of biological responses Cancer Res. 1992, 52, 202-208
-
(1992)
Cancer Res.
, vol.52
, pp. 202-208
-
-
Hasler, C.M.1
Acs, G.2
Blumberg, P.M.3
-
269
-
-
85030096213
-
-
U.S. Food and Drug Administration. 2012 Novel New DrugsSummary; FDA: Washington, DC
-
U.S. Food and Drug Administration. 2012 Novel New DrugsSummary; FDA: Washington, DC, 2013. www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/DrugInnovation/UCM337830.pdf.
-
(2013)
-
-
-
270
-
-
0000560130
-
In/out Isomerism
-
Alder, R. W.; East, S. P. In/out Isomerism Chem. Rev. 1996, 96, 2097-2112 10.1021/cr940246k
-
(1996)
Chem. Rev.
, vol.96
, pp. 2097-2112
-
-
Alder, R.W.1
East, S.P.2
-
271
-
-
30744431862
-
Total Syntheses of Ingenol
-
Kuwajima, I.; Tanino, K. Total Syntheses of Ingenol Chem. Rev. 2005, 105, 4661-4670 10.1021/cr040636z
-
(2005)
Chem. Rev.
, vol.105
, pp. 4661-4670
-
-
Kuwajima, I.1
Tanino, K.2
-
272
-
-
0037151671
-
The First Total Synthesis of (±)-Ingenol
-
Winkler, J. D.; Rouse, M. B.; Greaney, M. F.; Harrison, S. J.; Jeon, Y. T. The First Total Synthesis of (±)-Ingenol J. Am. Chem. Soc. 2002, 124, 9726-9728 10.1021/ja026600a
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 9726-9728
-
-
Winkler, J.D.1
Rouse, M.B.2
Greaney, M.F.3
Harrison, S.J.4
Jeon, Y.T.5
-
273
-
-
0037433234
-
Total Synthesis of Ingenol
-
Tanino, K.; Onuki, K.; Asano, K.; Miyashita, M.; Nakamura, T.; Takahashi, Y.; Kuwajima, I. Total Synthesis of Ingenol J. Am. Chem. Soc. 2003, 125, 1498-1500 10.1021/ja029226n
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 1498-1500
-
-
Tanino, K.1
Onuki, K.2
Asano, K.3
Miyashita, M.4
Nakamura, T.5
Takahashi, Y.6
Kuwajima, I.7
-
274
-
-
8644260018
-
Formal Synthesis of Optically Active Ingenol via Ring-Closing Olefin Metathesis
-
Watanabe, K.; Suzuki, Y.; Aoki, K.; Sakakura, A.; Suenaga, K.; Kigoshi, H. Formal Synthesis of Optically Active Ingenol via Ring-Closing Olefin Metathesis J. Org. Chem. 2004, 69, 7802-7808 10.1021/jo048833l
-
(2004)
J. Org. Chem.
, vol.69
, pp. 7802-7808
-
-
Watanabe, K.1
Suzuki, Y.2
Aoki, K.3
Sakakura, A.4
Suenaga, K.5
Kigoshi, H.6
-
275
-
-
11444258937
-
Total Synthesis of Ingenol
-
Nickel, A.; Maruyama, T.; Tang, H.; Murphy, P. D.; Greene, B.; Yusuff, N.; Wood, J. L. Total Synthesis of Ingenol J. Am. Chem. Soc. 2004, 126, 16300-16301 10.1021/ja044123l
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16300-16301
-
-
Nickel, A.1
Maruyama, T.2
Tang, H.3
Murphy, P.D.4
Greene, B.5
Yusuff, N.6
Wood, J.L.7
-
276
-
-
84882907547
-
14-Step Synthesis of (+)-Ingenol from (+)-3-Carene
-
Jørgensen, L.; McKerrall, S. J.; Kuttruff, C. A.; Ungeheuer, F.; Felding, J.; Baran, P. S. 14-Step Synthesis of (+)-Ingenol from (+)-3-Carene Science 2013, 341, 878-882 10.1126/science.1241606
-
(2013)
Science
, vol.341
, pp. 878-882
-
-
Jørgensen, L.1
McKerrall, S.J.2
Kuttruff, C.A.3
Ungeheuer, F.4
Felding, J.5
Baran, P.S.6
-
277
-
-
0001252145
-
A Solution to the in,out-Bicyclo[4.4.1]undecan-7-one Problem Inherent in Ingenane Total Synthesis
-
Funk, R. L.; Olmstead, T. A.; Parvez, M. A Solution to the in,out-Bicyclo[4.4.1]undecan-7-one Problem Inherent in Ingenane Total Synthesis J. Am. Chem. Soc. 1988, 110, 3298-3300 10.1021/ja00218a049
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 3298-3300
-
-
Funk, R.L.1
Olmstead, T.A.2
Parvez, M.3
-
278
-
-
0035902262
-
Progress toward the Total Synthesis of Ingenol: Construction of the Complete Carbocyclic Skeleton
-
Tang, H.; Yusuff, N.; Wood, J. L. Progress toward the Total Synthesis of Ingenol: Construction of the Complete Carbocyclic Skeleton Org. Lett. 2001, 3, 1563-1566 10.1021/ol015855a
-
(2001)
Org. Lett.
, vol.3
, pp. 1563-1566
-
-
Tang, H.1
Yusuff, N.2
Wood, J.L.3
-
279
-
-
22744448499
-
Metathesis Reactions in Total Synthesis
-
Nicolaou, K. C.; Bulger, P. G.; Sarlah, D. Metathesis Reactions in Total Synthesis Angew. Chem., Int. Ed. 2005, 44, 4490-4527 10.1002/anie.200500369
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4490-4527
-
-
Nicolaou, K.C.1
Bulger, P.G.2
Sarlah, D.3
-
280
-
-
84898979567
-
Development of a Concise Synthesis of (+)-Ingenol
-
McKerrall, S. J.; Jørgensen, L.; Kuttruff, C. A.; Ungeheuer, F.; Baran, P. S. Development of a Concise Synthesis of (+)-Ingenol J. Am. Chem. Soc. 2014, 136, 5799-5810 10.1021/ja501881p
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5799-5810
-
-
McKerrall, S.J.1
Jørgensen, L.2
Kuttruff, C.A.3
Ungeheuer, F.4
Baran, P.S.5
-
281
-
-
11244300691
-
Rapid Access to the "in,out"-Tetracyclic Core of Ingenol
-
Epstein, O. L.; Cha, J. K. Rapid Access to the "in,out"-Tetracyclic Core of Ingenol Angew. Chem., Int. Ed. 2004, 44, 121-123 10.1002/anie.200461807
-
(2004)
Angew. Chem., Int. Ed.
, vol.44
, pp. 121-123
-
-
Epstein, O.L.1
Cha, J.K.2
-
282
-
-
0037198748
-
An Allenic Pauson-Khand-Type Reaction: A Reversal in π-Bond Selectivity and the Formation of Seven-Membered Rings
-
Brummond, K. M.; Chen, H.; Fisher, K. D.; Kerekes, A. D.; Rickards, B.; Sill, P. C.; Geib, S. J. An Allenic Pauson-Khand-Type Reaction: A Reversal in π-Bond Selectivity and the Formation of Seven-Membered Rings Org. Lett. 2002, 4, 1931-1934 10.1021/ol025955w
-
(2002)
Org. Lett.
, vol.4
, pp. 1931-1934
-
-
Brummond, K.M.1
Chen, H.2
Fisher, K.D.3
Kerekes, A.D.4
Rickards, B.5
Sill, P.C.6
Geib, S.J.7
-
283
-
-
34250948041
-
Über die Wirksamkeit von Substanzen aus dem Krotonöl
-
Bohm, R.; Flaschentrager, B.; Lendle, L. Über die Wirksamkeit von Substanzen aus dem Krotonöl Arch. Exp. Pathol. Pharmakol. 1934, 177, 212-220 10.1007/BF02023126
-
(1934)
Arch. Exp. Pathol. Pharmakol.
, vol.177
, pp. 212-220
-
-
Bohm, R.1
Flaschentrager, B.2
Lendle, L.3
-
284
-
-
84929335336
-
Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families
-
Wang, H.-B.; Wang, X.-Y.; Liu, L.-P.; Qin, G.-W.; Kang, T.-G. Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families Chem. Rev. 2015, 115, 2975-3011 10.1021/cr200397n
-
(2015)
Chem. Rev.
, vol.115
, pp. 2975-3011
-
-
Wang, H.-B.1
Wang, X.-Y.2
Liu, L.-P.3
Qin, G.-W.4
Kang, T.-G.5
-
285
-
-
84890417449
-
Regulation of immune system cell functions by protein kinase C
-
Isakov, N.; Altman, A. Regulation of immune system cell functions by protein kinase C Front. Immunol. 2013, 4, 384 10.3389/fimmu.2013.00384
-
(2013)
Front. Immunol.
, vol.4
, pp. 384
-
-
Isakov, N.1
Altman, A.2
-
286
-
-
84864939469
-
Protein Kinase C: One Pathway towards the Eradication of Latent HIV-1 Reservoirs
-
McKernan, L. N.; Momjian, D.; Kulkosky, J. Protein Kinase C: One Pathway towards the Eradication of Latent HIV-1 Reservoirs Adv. Virol. 2012, 2012, 805347 10.1155/2012/805347
-
(2012)
Adv. Virol.
, vol.2012
, pp. 805347
-
-
McKernan, L.N.1
Momjian, D.2
Kulkosky, J.3
-
287
-
-
34250902930
-
Targeting the protein kinase C family: Are we there yet?
-
Mackay, H. J.; Twelves, C. J. Targeting the protein kinase C family: are we there yet? Nat. Rev. Cancer 2007, 7, 554-562 10.1038/nrc2168
-
(2007)
Nat. Rev. Cancer
, vol.7
, pp. 554-562
-
-
Mackay, H.J.1
Twelves, C.J.2
-
288
-
-
0024827695
-
Studies on tumor promoters. 7. the synthesis of a potentially general precursor of the tiglianes, daphnanes, and ingenanes
-
Wender, P. A.; Lee, H. Y.; Wilhelm, R. S.; Williams, P. D. Studies on tumor promoters. 7. The synthesis of a potentially general precursor of the tiglianes, daphnanes, and ingenanes J. Am. Chem. Soc. 1989, 111, 8954-8957 10.1021/ja00206a049
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 8954-8957
-
-
Wender, P.A.1
Lee, H.Y.2
Wilhelm, R.S.3
Williams, P.D.4
-
289
-
-
0024847252
-
Studies on tumor promoters. 8. the synthesis of phorbol
-
Wender, P. A.; Kogen, H.; Lee, H. Y.; Munger, J. D.; Wilhelm, R. S.; Williams, P. D. Studies on tumor promoters. 8. The synthesis of phorbol J. Am. Chem. Soc. 1989, 111, 8957-8958 10.1021/ja00206a050
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 8957-8958
-
-
Wender, P.A.1
Kogen, H.2
Lee, H.Y.3
Munger, J.D.4
Wilhelm, R.S.5
Williams, P.D.6
-
290
-
-
0025039722
-
Studies on tumor promoters. 9. A second-generation synthesis of phorbol
-
Wender, P. A.; McDonald, F. E. Studies on tumor promoters. 9. A second-generation synthesis of phorbol J. Am. Chem. Soc. 1990, 112, 4956-4958 10.1021/ja00168a050
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4956-4958
-
-
Wender, P.A.1
McDonald, F.E.2
-
291
-
-
0030884126
-
The first formal asymmetric synthesis of phorbol
-
Wender, P. A.; Rice, K. D.; Schnute, M. E. The first formal asymmetric synthesis of phorbol J. Am. Chem. Soc. 1997, 119, 7897-7898 10.1021/ja9706256
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 7897-7898
-
-
Wender, P.A.1
Rice, K.D.2
Schnute, M.E.3
-
292
-
-
0034824177
-
Formal Synthesis of (+)-Phorbol
-
Lee, K.; Cha, J. K. Formal Synthesis of (+)-Phorbol J. Am. Chem. Soc. 2001, 123, 5590-5591 10.1021/ja010643u
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5590-5591
-
-
Lee, K.1
Cha, J.K.2
-
293
-
-
84963500354
-
Nineteen-step total synthesis of (+)-phorbol
-
Kawamura, S.; Chu, H.; Felding, J.; Baran, P. S. Nineteen-step total synthesis of (+)-phorbol Nature 2016, 532, 90-93 10.1038/nature17153
-
(2016)
Nature
, vol.532
, pp. 90-93
-
-
Kawamura, S.1
Chu, H.2
Felding, J.3
Baran, P.S.4
-
294
-
-
84876541085
-
Enhanced Reactivity in Dioxirane C-H Oxidations via Strain Release: A Computational and Experimental Study
-
Zou, L.; Paton, R. S.; Eschenmoser, A.; Newhouse, T. R.; Baran, P. S.; Houk, K. N. Enhanced Reactivity in Dioxirane C-H Oxidations via Strain Release: A Computational and Experimental Study J. Org. Chem. 2013, 78, 4037-4048 10.1021/jo400350v
-
(2013)
J. Org. Chem.
, vol.78
, pp. 4037-4048
-
-
Zou, L.1
Paton, R.S.2
Eschenmoser, A.3
Newhouse, T.R.4
Baran, P.S.5
Houk, K.N.6
-
295
-
-
0001742543
-
Dioxiranes: A new class of powerful oxidants
-
Adam, W.; Curci, R.; Edwards, J. O. Dioxiranes: a new class of powerful oxidants Acc. Chem. Res. 1989, 22, 205-211 10.1021/ar00162a002
-
(1989)
Acc. Chem. Res.
, vol.22
, pp. 205-211
-
-
Adam, W.1
Curci, R.2
Edwards, J.O.3
-
296
-
-
84973826074
-
Frhr. Über den Giftstoff im Krotonöl. II. Zur Konstitution von Krotophorbolon
-
Flaschenträger, B.; von Falkenhausen, F. Frhr. Über den Giftstoff im Krotonöl. II. Zur Konstitution von Krotophorbolon Justus Liebigs Ann. Chem. 1934, 514, 252-260 10.1002/jlac.19345140113
-
(1934)
Justus Liebigs Ann. Chem.
, vol.514
, pp. 252-260
-
-
Flaschenträger, B.1
Von Falkenhausen, F.2
-
297
-
-
78650141070
-
Diterpenoids from the roots of Euphorbia fischeriana
-
Wang, H. B.; Chu, W.-J.; Wang, Y.; Ji, P.; Wang, Y.-B.; Yu, Q.; Qin, G.-W. Diterpenoids from the roots of Euphorbia fischeriana J. Asian Nat. Prod. Res. 2010, 12, 1038-1043 10.1080/10286020.2010.532490
-
(2010)
J. Asian Nat. Prod. Res.
, vol.12
, pp. 1038-1043
-
-
Wang, H.B.1
Chu, W.-J.2
Wang, Y.3
Ji, P.4
Wang, Y.-B.5
Yu, Q.6
Qin, G.-W.7
-
298
-
-
43249122214
-
Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV
-
Wender, P. A.; Kee, J.-M.; Warrington, J. M. Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV Science 2008, 320, 649-652 10.1126/science.1154690
-
(2008)
Science
, vol.320
, pp. 649-652
-
-
Wender, P.A.1
Kee, J.-M.2
Warrington, J.M.3
-
299
-
-
84880351418
-
Highly potent, synthetically accessible prostratin analogs induce latent HIV expression in vitro and ex vivo
-
Beans, E. J.; Fournogerakis, D.; Gauntlett, C.; Heumann, L. V.; Kramer, R.; Marsden, M. D.; Murray, D.; Chun, T.-W.; Zack, J. A.; Wender, P. A. Highly potent, synthetically accessible prostratin analogs induce latent HIV expression in vitro and ex vivo Proc. Natl. Acad. Sci. U. S. A. 2013, 110, 11698-11703 10.1073/pnas.1302634110
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 11698-11703
-
-
Beans, E.J.1
Fournogerakis, D.2
Gauntlett, C.3
Heumann, L.V.4
Kramer, R.5
Marsden, M.D.6
Murray, D.7
Chun, T.-W.8
Zack, J.A.9
Wender, P.A.10
-
300
-
-
84954368405
-
Total Synthesis of Crotophorbolone
-
Asaba, T.; Katoh, Y.; Urabe, D.; Inoue, M. Total Synthesis of Crotophorbolone Angew. Chem., Int. Ed. 2015, 54, 14457-14461 10.1002/anie.201509160
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 14457-14461
-
-
Asaba, T.1
Katoh, Y.2
Urabe, D.3
Inoue, M.4
-
301
-
-
0342379406
-
The Kharasch Reagent. Regioselective Generation of Dienol Ethers from Enones
-
Krafft, M. E.; Holton, R. A. The Kharasch Reagent. Regioselective Generation of Dienol Ethers from Enones J. Am. Chem. Soc. 1984, 106, 7619-7621 10.1021/ja00336a051
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 7619-7621
-
-
Krafft, M.E.1
Holton, R.A.2
-
302
-
-
0000702878
-
Radical reactions in natural product synthesis
-
Jasperse, C. P.; Curran, D. P.; Fevig, T. L. Radical reactions in natural product synthesis Chem. Rev. 1991, 91, 1237-1286 10.1021/cr00006a006
-
(1991)
Chem. Rev.
, vol.91
, pp. 1237-1286
-
-
Jasperse, C.P.1
Curran, D.P.2
Fevig, T.L.3
-
305
-
-
84990060779
-
Radicals: Reactive Intermediates with Translational Potential
-
Yan, M.; Lo, J. C.; Edwards, J. T.; Baran, P. S. Radicals: Reactive Intermediates with Translational Potential J. Am. Chem. Soc. 2016, 138, 12692-12714 10.1021/jacs.6b08856
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 12692-12714
-
-
Yan, M.1
Lo, J.C.2
Edwards, J.T.3
Baran, P.S.4
-
306
-
-
0000355156
-
The pseudopterosins: Anti-inflammatory and analgesic natural products from the sea whip Pseudoptergorgia elisabethae
-
Look, S. A.; Fenical, W.; Jacobs, R. S.; Clardy, J. The pseudopterosins: Anti-inflammatory and analgesic natural products from the sea whip Pseudoptergorgia elisabethae Proc. Natl. Acad. Sci. U. S. A. 1986, 83, 6238-6240 10.1073/pnas.83.17.6238
-
(1986)
Proc. Natl. Acad. Sci. U. S. A.
, vol.83
, pp. 6238-6240
-
-
Look, S.A.1
Fenical, W.2
Jacobs, R.S.3
Clardy, J.4
-
307
-
-
0023877469
-
Total synthesis of (-)-pseudopterosin A
-
Broka, C. A.; Chan, S.; Peterson, B. Total synthesis of (-)-pseudopterosin A J. Org. Chem. 1988, 53, 1584-1586 10.1021/jo00242a053
-
(1988)
J. Org. Chem.
, vol.53
, pp. 1584-1586
-
-
Broka, C.A.1
Chan, S.2
Peterson, B.3
-
308
-
-
0024348148
-
Enantiospecific total synthesis of pseudopterosins A and e
-
Corey, E. J.; Carpino, P. Enantiospecific total synthesis of pseudopterosins A and E J. Am. Chem. Soc. 1989, 111, 5472-5474 10.1021/ja00196a067
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 5472-5474
-
-
Corey, E.J.1
Carpino, P.2
-
309
-
-
0025351606
-
A new enantiospecific route to the pseudopterosins
-
Corey, E. J.; Carpino, P. A new enantiospecific route to the pseudopterosins Tetrahedron Lett. 1990, 31, 3857-3858 10.1016/S0040-4039(00)97487-2
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 3857-3858
-
-
Corey, E.J.1
Carpino, P.2
-
310
-
-
0025878235
-
Controlling benzylic functionality and stereochemistry: 1. Synthesis of the secopseudopterosin aglycone
-
McCombie, S. W.; Cox, B.; Lin, S.-I.; Ganguly, A. K.; McPhail, A. T. Controlling benzylic functionality and stereochemistry: 1. Synthesis of the secopseudopterosin aglycone Tetrahedron Lett. 1991, 32, 2083-2086 10.1016/S0040-4039(00)71242-1
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2083-2086
-
-
McCombie, S.W.1
Cox, B.2
Lin, S.-I.3
Ganguly, A.K.4
McPhail, A.T.5
-
311
-
-
85022401078
-
Controlling Benzylic and Anomeric Functionality and Stereochemistry: Methodology and Syntheses Utilizing Intramolecular Ionic Hydrogenation
-
McCombie, S. W.; Ortiz, C.; Cox, B.; Ganguly, A. K. Controlling Benzylic and Anomeric Functionality and Stereochemistry: Methodology and Syntheses Utilizing Intramolecular Ionic Hydrogenation Synlett 1993, 1993, 541-547 10.1055/s-1993-22522
-
(1993)
Synlett
, vol.1993
, pp. 541-547
-
-
McCombie, S.W.1
Ortiz, C.2
Cox, B.3
Ganguly, A.K.4
-
312
-
-
0028860543
-
Total synthesis of pseudopterosin A and e aglycon
-
Buszek, K. R.; Bixby, D. L. Total synthesis of pseudopterosin A and E aglycon Tetrahedron Lett. 1995, 36, 9129-9132 10.1016/0040-4039(95)01981-M
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 9129-9132
-
-
Buszek, K.R.1
Bixby, D.L.2
-
313
-
-
0029763519
-
A synthetic approach to the pseudopterosins
-
Gill, S.; Kocienski, P.; Kohler, A.; Pontiroli, A.; Qun, L. A synthetic approach to the pseudopterosins Chem. Commun. 1996, 1743-1744 10.1039/cc9960001743
-
(1996)
Chem. Commun.
, pp. 1743-1744
-
-
Gill, S.1
Kocienski, P.2
Kohler, A.3
Pontiroli, A.4
Qun, L.5
-
314
-
-
0030913414
-
3 complexes in organic synthesis: A short and highly selective synthesis of the 18-nor-seco-pseudopterosin aglycone
-
3 complexes in organic synthesis: A short and highly selective synthesis of the 18-nor-seco-pseudopterosin aglycone Tetrahedron Lett. 1997, 38, 4545-4548 10.1016/S0040-4039(97)00995-7
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 4545-4548
-
-
Majdalani, A.1
Schmalz, H.-G.2
-
315
-
-
0002931771
-
Enantioselective Synthesis of the Aglycones of Pseudopterosin and seco-Pseudopterosin via a Common Synthetic Intermediate
-
Majdalani, A.; Schmalz, H.-G. Enantioselective Synthesis of the Aglycones of Pseudopterosin and seco-Pseudopterosin via a Common Synthetic Intermediate Synlett 1997, 1997, 1303-1305 10.1055/s-1997-1012
-
(1997)
Synlett
, vol.1997
, pp. 1303-1305
-
-
Majdalani, A.1
Schmalz, H.-G.2
-
316
-
-
33748653813
-
Synthetic approaches to pseudopterosin G aglycone dimethyl ether
-
LeBrazidec, J.-Y.; Kocienski, P. J.; Connolly, J. D.; Muir, K. W. Synthetic approaches to pseudopterosin G aglycone dimethyl ether J. Chem. Soc., Perkin Trans. 1 1998, 2475-2478 10.1039/a803888k
-
(1998)
J. Chem. Soc., Perkin Trans. 1
, pp. 2475-2478
-
-
LeBrazidec, J.-Y.1
Kocienski, P.J.2
Connolly, J.D.3
Muir, K.W.4
-
317
-
-
0032539199
-
A Direct and Efficient Stereocontrolled Synthetic Route to the Pseudopterosins, Potent Marine Antiinflamatory Agents
-
Corey, E. J.; Lazerwith, S. E. A Direct and Efficient Stereocontrolled Synthetic Route to the Pseudopterosins, Potent Marine Antiinflamatory Agents J. Am. Chem. Soc. 1998, 120, 12777-12782 10.1021/ja983041s
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 12777-12782
-
-
Corey, E.J.1
Lazerwith, S.E.2
-
318
-
-
0034740837
-
Enantiospecific syntheses of pseudopterosin aglycones. Part 2. Synthesis of pseudopterosin K-L aglycone and pseudopterosin A-F aglycone via a B→BA→BAC annulation strategy
-
Kocienski, P. J.; Pontiroli, A.; Qun, L. Enantiospecific syntheses of pseudopterosin aglycones. Part 2. Synthesis of pseudopterosin K-L aglycone and pseudopterosin A-F aglycone via a B→BA→BAC annulation strategy J. Chem. Soc. Perkin Trans 1 2001, 2356-2366 10.1039/b102961b
-
(2001)
J. Chem. Soc. Perkin Trans 1
, pp. 2356-2366
-
-
Kocienski, P.J.1
Pontiroli, A.2
Qun, L.3
-
319
-
-
1242273585
-
Total synthesis of (±)-pseudopterosin A-F and K-L aglycone
-
Harrowven, D. C.; Tyte, M. J. Total synthesis of (±)-pseudopterosin A-F and K-L aglycone Tetrahedron Lett. 2004, 45, 2089-2091 10.1016/j.tetlet.2004.01.060
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 2089-2091
-
-
Harrowven, D.C.1
Tyte, M.J.2
-
320
-
-
79954490071
-
Ethylene in organic synthesis. Repetitive hydrovinylation of alkenes for highly enantioselective syntheses of pseudopterosins
-
Mans, D. J.; Cox, G. A.; RajanBabu, T. V. Ethylene in organic synthesis. Repetitive hydrovinylation of alkenes for highly enantioselective syntheses of pseudopterosins J. Am. Chem. Soc. 2011, 133, 5776-5779 10.1021/ja201321v
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 5776-5779
-
-
Mans, D.J.1
Cox, G.A.2
RajanBabu, T.V.3
-
321
-
-
84865478752
-
A synthesis of the pseudopterosin A-F aglycone
-
Cooksey, J. P.; Kocieński, P. J.; Schmidt, A. W.; Snaddon, T. N.; Kilner, C. A. A synthesis of the pseudopterosin A-F aglycone Synthesis 2012, 44, 2779-2785 10.1055/s-0032-1316643
-
(2012)
Synthesis
, vol.44
, pp. 2779-2785
-
-
Cooksey, J.P.1
Kocieński, P.J.2
Schmidt, A.W.3
Snaddon, T.N.4
Kilner, C.A.5
-
322
-
-
84902667388
-
Total Synthesis of (+)-Ileabethoxazole via an Iron-Mediated Pauson-Khand [2 + 2+1] Carbocyclization
-
Williams, D. R.; Shah, A. A. Total Synthesis of (+)-Ileabethoxazole via an Iron-Mediated Pauson-Khand [2 + 2+1] Carbocyclization J. Am. Chem. Soc. 2014, 136, 8829-8836 10.1021/ja5043462
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 8829-8836
-
-
Williams, D.R.1
Shah, A.A.2
-
323
-
-
84926207825
-
Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions
-
Newton, C. G.; Drew, S. L.; Lawrence, A. L.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions Nat. Chem. 2015, 7, 82-86 10.1038/nchem.2112
-
(2015)
Nat. Chem.
, vol.7
, pp. 82-86
-
-
Newton, C.G.1
Drew, S.L.2
Lawrence, A.L.3
Willis, A.C.4
Paddon-Row, M.N.5
Sherburn, M.S.6
-
324
-
-
0033549680
-
Novel Antimycobacterial Benzoxazole Alkaloids, from the West Indian Sea Whip Pseudopterogorgia elisabethae
-
Rodríguez, A. D.; Ramírez, C.; Rodríguez, I. I.; González, E. Novel Antimycobacterial Benzoxazole Alkaloids, from the West Indian Sea Whip Pseudopterogorgia elisabethae Org. Lett. 1999, 1, 527-530 10.1021/ol9907116
-
(1999)
Org. Lett.
, vol.1
, pp. 527-530
-
-
Rodríguez, A.D.1
Ramírez, C.2
Rodríguez, I.I.3
González, E.4
-
325
-
-
0034720927
-
Syntheses and Stereochemical Revision of Pseudopterosin G-J Aglycon and Helioporin e
-
Lazerwith, S. E.; Johnson, T. W.; Corey, E. J. Syntheses and Stereochemical Revision of Pseudopterosin G-J Aglycon and Helioporin E Org. Lett. 2000, 2, 2389-2392 10.1021/ol006192k
-
(2000)
Org. Lett.
, vol.2
, pp. 2389-2392
-
-
Lazerwith, S.E.1
Johnson, T.W.2
Corey, E.J.3
-
326
-
-
15444378803
-
Chasing Molecules That Were Never There: Misassigned Natural Products and the Role of Chemical Synthesis in Modern Structure Elucidation
-
Nicolaou, K. C.; Snyder, S. A. Chasing Molecules That Were Never There: Misassigned Natural Products and the Role of Chemical Synthesis in Modern Structure Elucidation Angew. Chem., Int. Ed. 2005, 44, 1012-1044 10.1002/anie.200460864
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 1012-1044
-
-
Nicolaou, K.C.1
Snyder, S.A.2
-
327
-
-
0242299243
-
First Enantiospecific Total Synthesis of the Antitubercular Marine Natural Product Pseudopteroxazole. Revision of Assigned Stereochemistry
-
Davidson, J. P.; Corey, E. J. First Enantiospecific Total Synthesis of the Antitubercular Marine Natural Product Pseudopteroxazole. Revision of Assigned Stereochemistry J. Am. Chem. Soc. 2003, 125, 13486-13489 10.1021/ja0378916
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 13486-13489
-
-
Davidson, J.P.1
Corey, E.J.2
-
328
-
-
23944487696
-
Benzothiazines in Synthesis. A Total Synthesis of Pseudopteroxazole
-
Harmata, M.; Hong, X. Benzothiazines in Synthesis. A Total Synthesis of Pseudopteroxazole Org. Lett. 2005, 7, 3581-3583 10.1021/ol0515412
-
(2005)
Org. Lett.
, vol.7
, pp. 3581-3583
-
-
Harmata, M.1
Hong, X.2
-
329
-
-
84958281141
-
Total Synthesis of Ileabethoxazole, Pseudopteroxazole and seco-Pseudopteroxazole
-
Yang, M.; Yang, X.; Sun, H.; Li, A. Total Synthesis of Ileabethoxazole, Pseudopteroxazole and seco-Pseudopteroxazole Angew. Chem., Int. Ed. 2016, 55, 2851-2855 10.1002/anie.201510568
-
(2016)
Angew. Chem., Int. Ed.
, vol.55
, pp. 2851-2855
-
-
Yang, M.1
Yang, X.2
Sun, H.3
Li, A.4
-
330
-
-
84971330884
-
Enantioselective Total Syntheses of Various Amphilectane and Serrulatane Diterpenoids via Cope Rearrangements
-
Yu, X.; Su, F.; Liu, C.; Yuan, H.; Zhao, S.; Zhou, Z.; Quan, T.; Luo, T. Enantioselective Total Syntheses of Various Amphilectane and Serrulatane Diterpenoids via Cope Rearrangements J. Am. Chem. Soc. 2016, 138, 6261-6270 10.1021/jacs.6b02624
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 6261-6270
-
-
Yu, X.1
Su, F.2
Liu, C.3
Yuan, H.4
Zhao, S.5
Zhou, Z.6
Quan, T.7
Luo, T.8
-
331
-
-
33645239517
-
Hydroboration of terpenes - VIII: Cyclic hydroboration of D-(+)-limonene. A stereoselective synthesis of D-(-)-(1R, 2R, 4R)-limonene-2,9-diol and D-(-)-(1R, 2R, 4R)-carvomenthol
-
Brown, H. C.; Pfaffenberger, C. D. Hydroboration of terpenes-VIII: Cyclic hydroboration of D-(+)-limonene. A stereoselective synthesis of D-(-)-(1R, 2R, 4R)-limonene-2,9-diol and D-(-)-(1R, 2R, 4R)-carvomenthol Tetrahedron 1975, 31, 925-928 10.1016/0040-4020(75)80101-3
-
(1975)
Tetrahedron
, vol.31
, pp. 925-928
-
-
Brown, H.C.1
Pfaffenberger, C.D.2
-
332
-
-
84903434851
-
Rearrangement of N-Oxyenamines and Related Reactions
-
Tabolin, A. A.; Ioffe, S. L. Rearrangement of N-Oxyenamines and Related Reactions Chem. Rev. 2014, 114, 5426-5476 10.1021/cr400196x
-
(2014)
Chem. Rev.
, vol.114
, pp. 5426-5476
-
-
Tabolin, A.A.1
Ioffe, S.L.2
-
333
-
-
0000169733
-
An E-selective 1,3-diene synthesis from moderated ylides and aldehydes
-
Vedejs, E.; Fang, H. W. An E-selective 1,3-diene synthesis from moderated ylides and aldehydes J. Org. Chem. 1984, 49, 210-212 10.1021/jo00175a057
-
(1984)
J. Org. Chem.
, vol.49
, pp. 210-212
-
-
Vedejs, E.1
Fang, H.W.2
-
334
-
-
23944520724
-
Marine Natural Products from Pseudopterogorgia elisabethae: Structures, Biosynthesis, Pharmacology, and Total Synthesis
-
Heckrodt, T. J.; Mulzer, J. Marine Natural Products from Pseudopterogorgia elisabethae: Structures, Biosynthesis, Pharmacology, and Total Synthesis Top. Curr. Chem. 2005, 244, 1-41 10.1007/b96886
-
(2005)
Top. Curr. Chem.
, vol.244
, pp. 1-41
-
-
Heckrodt, T.J.1
Mulzer, J.2
-
335
-
-
76449107766
-
Synthesis of a key intermediate for the total synthesis of pseudopteroxazole
-
Yadav, J. S.; Bhasker, E. V.; Srihari, P. Synthesis of a key intermediate for the total synthesis of pseudopteroxazole Tetrahedron 2010, 66, 1997-2004 10.1016/j.tet.2010.01.054
-
(2010)
Tetrahedron
, vol.66
, pp. 1997-2004
-
-
Yadav, J.S.1
Bhasker, E.V.2
Srihari, P.3
-
336
-
-
0025353115
-
Effects of organometals on the palladium-catalyzed carbopalladation-cross coupling for preparing stereodefined exocyclic alkenes
-
Negishi, E.; Noda, Y.; Lamaty, F.; Vawter, E. J. Effects of organometals on the palladium-catalyzed carbopalladation-cross coupling for preparing stereodefined exocyclic alkenes Tetrahedron Lett. 1990, 31, 4393-4396 10.1016/S0040-4039(00)97630-5
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 4393-4396
-
-
Negishi, E.1
Noda, Y.2
Lamaty, F.3
Vawter, E.J.4
-
337
-
-
4544224672
-
A straightforward and mild synthesis of functionalized 3-alkynoates
-
Suárez, A.; Fu, G. C. A straightforward and mild synthesis of functionalized 3-alkynoates Angew. Chem., Int. Ed. 2004, 43, 3580-3582 10.1002/anie.200454070
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 3580-3582
-
-
Suárez, A.1
Fu, G.C.2
-
338
-
-
69049104186
-
Enantioselective α-Arylation of Aldehydes via Organo-SOMO Catalysis. An Ortho-Selective Arylation Reaction Based on an Open-Shell Pathway
-
Conrad, J. C.; Kong, J.; Laforteza, B. N.; MacMillan, D. W. C. Enantioselective α-Arylation of Aldehydes via Organo-SOMO Catalysis. An Ortho-Selective Arylation Reaction Based on an Open-Shell Pathway J. Am. Chem. Soc. 2009, 131, 11640-11641 10.1021/ja9026902
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11640-11641
-
-
Conrad, J.C.1
Kong, J.2
Laforteza, B.N.3
MacMillan, D.W.C.4
-
339
-
-
33744994317
-
Platensimycin is a selective FabF inhibitor with potent antibiotic properties
-
Wang, J.; Soisson, S. M.; Young, K.; Shoop, W.; Kodali, S.; Galgoci, A.; Painter, R.; Parthasarathy, G.; Tang, Y. S.; Cummings, R. et al. Platensimycin is a selective FabF inhibitor with potent antibiotic properties Nature 2006, 441, 358-361 10.1038/nature04784
-
(2006)
Nature
, vol.441
, pp. 358-361
-
-
Wang, J.1
Soisson, S.M.2
Young, K.3
Shoop, W.4
Kodali, S.5
Galgoci, A.6
Painter, R.7
Parthasarathy, G.8
Tang, Y.S.9
Cummings, R.10
-
340
-
-
33748482185
-
Isolation, Structure, and Absolute Stereochemistry of Platensimycin, A Broad Spectrum Antibiotic Discovered Using an Antisense Differential Sensitivity Strategy
-
Singh, S. B.; Jayasuriya, H.; Ondeyka, J. G.; Herath, K. B.; Zhang, C.; Zink, D. L.; Tsou, N. N.; Ball, R. G.; Basilio, A.; Genilloud, O. et al. Isolation, Structure, and Absolute Stereochemistry of Platensimycin, A Broad Spectrum Antibiotic Discovered Using an Antisense Differential Sensitivity Strategy J. Am. Chem. Soc. 2006, 128, 11916-11920 10.1021/ja062232p
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 11916-11920
-
-
Singh, S.B.1
Jayasuriya, H.2
Ondeyka, J.G.3
Herath, K.B.4
Zhang, C.5
Zink, D.L.6
Tsou, N.N.7
Ball, R.G.8
Basilio, A.9
Genilloud, O.10
-
341
-
-
77950790357
-
Discovery and syntheses of "superbug challengers" - Platensimycin and platencin
-
Palanichamy, K.; Kaliappan, K. P. Discovery and syntheses of "superbug challengers"-platensimycin and platencin Chem.-Asian J. 2010, 5, 668-703 10.1002/asia.200900423
-
(2010)
Chem. - Asian J.
, vol.5
, pp. 668-703
-
-
Palanichamy, K.1
Kaliappan, K.P.2
-
342
-
-
80052101291
-
Platensimycin and its relatives: A recent story in the struggle to develop new naturally derived antibiotics
-
Saleem, M.; Hussain, H.; Ahmed, I.; van Ree, T.; Krohn, K. Platensimycin and its relatives: A recent story in the struggle to develop new naturally derived antibiotics Nat. Prod. Rep. 2011, 28, 1534-1579 10.1039/c1np00010a
-
(2011)
Nat. Prod. Rep.
, vol.28
, pp. 1534-1579
-
-
Saleem, M.1
Hussain, H.2
Ahmed, I.3
Van Ree, T.4
Krohn, K.5
-
343
-
-
82355175618
-
Platensimycin and platencin: Promising antibiotics for future application in human medicine
-
Martens, E.; Demain, A. L. Platensimycin and platencin: Promising antibiotics for future application in human medicine J. Antibiot. 2011, 64, 705-710 10.1038/ja.2011.80
-
(2011)
J. Antibiot.
, vol.64
, pp. 705-710
-
-
Martens, E.1
Demain, A.L.2
-
344
-
-
84884653895
-
The use of platensimycin and platencin to fight antibiotic resistance
-
Allahverdiyev, A. M.; Bagirova, M.; Abamor, E. S.; Ates, S. C.; Koc, R. C.; Miraloglu, M.; Elcicek, S.; Yaman, S.; Unal, G. The use of platensimycin and platencin to fight antibiotic resistance Infect. Drug Resist. 2013, 6, 99-114 10.2147/IDR.S25076
-
(2013)
Infect. Drug Resist.
, vol.6
, pp. 99-114
-
-
Allahverdiyev, A.M.1
Bagirova, M.2
Abamor, E.S.3
Ates, S.C.4
Koc, R.C.5
Miraloglu, M.6
Elcicek, S.7
Yaman, S.8
Unal, G.9
-
345
-
-
41949129210
-
Synthesis of Platensimycin
-
Tiefenbacher, K.; Mulzer, J. Synthesis of Platensimycin Angew. Chem., Int. Ed. 2008, 47, 2548-2555 10.1002/anie.200705303
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 2548-2555
-
-
Tiefenbacher, K.1
Mulzer, J.2
-
346
-
-
85030100506
-
A Review on Platensimycin: A Selective FabF Inhibitor
-
Das, M.; Ghosh, P. S.; Manna, K. A Review on Platensimycin: A Selective FabF Inhibitor Int. J. Med. Chem. 2016, 2016, 1-16 10.1155/2016/9706753
-
(2016)
Int. J. Med. Chem.
, vol.2016
, pp. 1-16
-
-
Das, M.1
Ghosh, P.S.2
Manna, K.3
-
347
-
-
33750629319
-
Total Synthesis of Platensimycin
-
Nicolaou, K. C.; Li, A.; Edmonds, D. J. Total Synthesis of Platensimycin Angew. Chem., Int. Ed. 2006, 45, 7086-7090 10.1002/anie.200603892
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 7086-7090
-
-
Nicolaou, K.C.1
Li, A.2
Edmonds, D.J.3
-
348
-
-
34250812701
-
Formal synthesis of (±)-platensimycin
-
Nicolaou, K. C.; Tang, Y.; Wang, J. Formal synthesis of (±)-platensimycin Chem. Commun. 2007, 1922-1923 10.1039/B704589A
-
(2007)
Chem. Commun.
, pp. 1922-1923
-
-
Nicolaou, K.C.1
Tang, Y.2
Wang, J.3
-
349
-
-
34250702223
-
Asymmetric Total Syntheses of Platensimycin
-
Nicolaou, K. C.; Edmonds, D. J.; Li, A.; Tria, G. S. Asymmetric Total Syntheses of Platensimycin Angew. Chem., Int. Ed. 2007, 46, 3942-3945 10.1002/anie.200700586
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 3942-3945
-
-
Nicolaou, K.C.1
Edmonds, D.J.2
Li, A.3
Tria, G.S.4
-
350
-
-
70450188974
-
Total Synthesis of Platensimycin and Related Natural Products
-
Nicolaou, K. C.; Li, A.; Edmonds, D. J.; Tria, G. S.; Ellery, S. P. Total Synthesis of Platensimycin and Related Natural Products J. Am. Chem. Soc. 2009, 131, 16905-16918 10.1021/ja9068003
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 16905-16918
-
-
Nicolaou, K.C.1
Li, A.2
Edmonds, D.J.3
Tria, G.S.4
Ellery, S.P.5
-
351
-
-
70349895948
-
Rhodium-Catalyzed Asymmetric Enyne Cycloisomerization of Terminal Alkynes and Formal Total Synthesis of (-)-Platensimycin
-
Nicolaou, K. C.; Li, A.; Ellery, S. P.; Edmonds, D. J. Rhodium-Catalyzed Asymmetric Enyne Cycloisomerization of Terminal Alkynes and Formal Total Synthesis of (-)-Platensimycin Angew. Chem., Int. Ed. 2009, 48, 6293-6295 10.1002/anie.200901992
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 6293-6295
-
-
Nicolaou, K.C.1
Li, A.2
Ellery, S.P.3
Edmonds, D.J.4
-
352
-
-
35649019236
-
Protecting-Group-Free Formal Synthesis of Platensimycin
-
Tiefenbacher, K.; Mulzer, J. Protecting-Group-Free Formal Synthesis of Platensimycin Angew. Chem., Int. Ed. 2007, 46, 8074-8075 10.1002/anie.200702852
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 8074-8075
-
-
Tiefenbacher, K.1
Mulzer, J.2
-
353
-
-
34248329634
-
Formal Synthesis of (±)-Platensimycin
-
Zou, Y.; Chen, C.-H.; Taylor, C. D.; Foxman, B. M.; Snider, B. B. Formal Synthesis of (±)-Platensimycin Org. Lett. 2007, 9, 1825-1828 10.1021/ol070563g
-
(2007)
Org. Lett.
, vol.9
, pp. 1825-1828
-
-
Zou, Y.1
Chen, C.-H.2
Taylor, C.D.3
Foxman, B.M.4
Snider, B.B.5
-
354
-
-
34547811676
-
Enantioselective Route to Platensimycin: An Intramolecular Robinson Annulation Approach
-
Li, P.; Payette, J. N.; Yamamoto, H. Enantioselective Route to Platensimycin: An Intramolecular Robinson Annulation Approach J. Am. Chem. Soc. 2007, 129, 9534-9535 10.1021/ja073547n
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9534-9535
-
-
Li, P.1
Payette, J.N.2
Yamamoto, H.3
-
355
-
-
36348961991
-
An Effective Enantioselective Route to the Platensimycin Core
-
Lalic, G.; Corey, E. J. An Effective Enantioselective Route to the Platensimycin Core Org. Lett. 2007, 9, 4921-4923 10.1021/ol702323s
-
(2007)
Org. Lett.
, vol.9
, pp. 4921-4923
-
-
Lalic, G.1
Corey, E.J.2
-
356
-
-
38549174642
-
A Chiral Pool Based Synthesis of Platensimycin
-
Nicolaou, K. C.; Pappo, D.; Tsang, K. Y.; Gibe, R.; Chen, D. Y.-K. A Chiral Pool Based Synthesis of Platensimycin Angew. Chem., Int. Ed. 2008, 47, 944-946 10.1002/anie.200705080
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 944-946
-
-
Nicolaou, K.C.1
Pappo, D.2
Tsang, K.Y.3
Gibe, R.4
Chen, D.Y.-K.5
-
357
-
-
47049122357
-
A Carbonyl Ylide Cycloaddition Approach to Platensimycin
-
Kim, C. H.; Jang, K. P.; Choi, S. Y.; Chung, Y. K.; Lee, E. A Carbonyl Ylide Cycloaddition Approach to Platensimycin Angew. Chem., Int. Ed. 2008, 47, 4009-4011 10.1002/anie.200800568
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 4009-4011
-
-
Kim, C.H.1
Jang, K.P.2
Choi, S.Y.3
Chung, Y.K.4
Lee, E.5
-
358
-
-
55949084611
-
Stereocontrolled Formal Synthesis of (±)-Platensimycin
-
Matsuo, J.-I.; Takeuchi, K.; Ishibashi, H. Stereocontrolled Formal Synthesis of (±)-Platensimycin Org. Lett. 2008, 10, 4049-4052 10.1021/ol801584r
-
(2008)
Org. Lett.
, vol.10
, pp. 4049-4052
-
-
Matsuo, J.-I.1
Takeuchi, K.2
Ishibashi, H.3
-
359
-
-
70350303174
-
A Concise Ring-Expansion Route to the Compact Core of Platensimycin
-
McGrath, N. A.; Bartlett, E. S.; Sittihan, S.; Njardarson, J. T. A Concise Ring-Expansion Route to the Compact Core of Platensimycin Angew. Chem., Int. Ed. 2009, 48, 8543-8546 10.1002/anie.200903347
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 8543-8546
-
-
McGrath, N.A.1
Bartlett, E.S.2
Sittihan, S.3
Njardarson, J.T.4
-
360
-
-
35048904473
-
Enantioselective Synthesis of (-)-Platensimycin Oxatetracyclic Core by Using an Intramolecular Diels-Alder Reaction
-
Ghosh, A. K.; Xi, K. Enantioselective Synthesis of (-)-Platensimycin Oxatetracyclic Core by Using an Intramolecular Diels-Alder Reaction Org. Lett. 2007, 9, 4013-4016 10.1021/ol701783z
-
(2007)
Org. Lett.
, vol.9
, pp. 4013-4016
-
-
Ghosh, A.K.1
Xi, K.2
-
361
-
-
67650545673
-
Stereoelectronic Effect for the Selectivity in C-H Insertion of Alkylidene Carbenes and Its Application to the Synthesis of Platensimycin
-
Yun, S. Y.; Zheng, J.-C.; Lee, D. Stereoelectronic Effect for the Selectivity in C-H Insertion of Alkylidene Carbenes and Its Application to the Synthesis of Platensimycin J. Am. Chem. Soc. 2009, 131, 8413-8415 10.1021/ja903526g
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8413-8415
-
-
Yun, S.Y.1
Zheng, J.-C.2
Lee, D.3
-
362
-
-
77957201390
-
An Oxidative Prins-Pinacol Tandem Process and its Application to the synthesis of (-)-Platensimycin
-
Beaulieu, M.-A.; Sabot, C.; Achache, N.; Guérard, K. C.; Canesi, S. An Oxidative Prins-Pinacol Tandem Process and its Application to the synthesis of (-)-Platensimycin Chem.-Eur. J. 2010, 16, 11224-11228 10.1002/chem.201001813
-
(2010)
Chem. - Eur. J.
, vol.16
, pp. 11224-11228
-
-
Beaulieu, M.-A.1
Sabot, C.2
Achache, N.3
Guérard, K.C.4
Canesi, S.5
-
363
-
-
78650376380
-
Concise Formal Total Synthesis of Platensimycin Mediated by a Stereoselective Autoxidation and Hydroxyl Group Directed Conjugative Reduction
-
Magnus, P.; Rivera, H.; Lynch, V. Concise Formal Total Synthesis of Platensimycin Mediated by a Stereoselective Autoxidation and Hydroxyl Group Directed Conjugative Reduction Org. Lett. 2010, 12, 5677-5679 10.1021/ol102557k
-
(2010)
Org. Lett.
, vol.12
, pp. 5677-5679
-
-
Magnus, P.1
Rivera, H.2
Lynch, V.3
-
364
-
-
78650174098
-
Enantioselective divergent approaches to both (-)-platensimycin and (-)-platencin
-
Hirai, S.; Nakada, M. Enantioselective divergent approaches to both (-)-platensimycin and (-)-platencin Tetrahedron 2011, 67, 518-530 10.1016/j.tet.2010.10.076
-
(2011)
Tetrahedron
, vol.67
, pp. 518-530
-
-
Hirai, S.1
Nakada, M.2
-
365
-
-
79955844784
-
Enantioselective Synthesis of the Tetracyclic Core of Platensimycin
-
Ueda, Y.; Iwahashi, K.; Iguchi, K.; Ito, H. Enantioselective Synthesis of the Tetracyclic Core of Platensimycin Synthesis 2011, 2011, 1532-1536 10.1055/s-0030-1260002
-
(2011)
Synthesis
, vol.2011
, pp. 1532-1536
-
-
Ueda, Y.1
Iwahashi, K.2
Iguchi, K.3
Ito, H.4
-
366
-
-
79955577386
-
Highly Substituted Oxabicyclic Derivatives from Furan: Synthesis of (±)-Platensimycin
-
Oblak, E. Z.; Wright, D. L. Highly Substituted Oxabicyclic Derivatives from Furan: Synthesis of (±)-Platensimycin Org. Lett. 2011, 13, 2263-2265 10.1021/ol2005775
-
(2011)
Org. Lett.
, vol.13
, pp. 2263-2265
-
-
Oblak, E.Z.1
Wright, D.L.2
-
367
-
-
84873354064
-
A Bifunctional Lewis Acid Induced Cascade Cyclization to the Tricyclic Core of ent-Kaurenoids and Its Application to the Formal Synthesis of (±)-Platensimycin
-
Zhu, L.; Han, Y.; Du, G.; Lee, C.-S. A Bifunctional Lewis Acid Induced Cascade Cyclization to the Tricyclic Core of ent-Kaurenoids and Its Application to the Formal Synthesis of (±)-Platensimycin Org. Lett. 2013, 15, 524-527 10.1021/ol3033412
-
(2013)
Org. Lett.
, vol.15
, pp. 524-527
-
-
Zhu, L.1
Han, Y.2
Du, G.3
Lee, C.-S.4
-
368
-
-
84875189849
-
Stereoselective Approach to the Racemic Oxatetracyclic Core of Platensimycin
-
Horii, S.; Torihata, M.; Nagasawa, T.; Kuwahara, S. Stereoselective Approach to the Racemic Oxatetracyclic Core of Platensimycin J. Org. Chem. 2013, 78, 2798-2801 10.1021/jo302813y
-
(2013)
J. Org. Chem.
, vol.78
, pp. 2798-2801
-
-
Horii, S.1
Torihata, M.2
Nagasawa, T.3
Kuwahara, S.4
-
369
-
-
84882295512
-
Formal Syntheses of (±)-Platensimycin and (±)-Platencin via a Dual-Mode Lewis Acid Induced Cascade Cyclization Approach
-
Zhu, L.; Zhou, C.; Yang, W.; He, S.; Cheng, G.-J.; Zhang, X.; Lee, C.-S. Formal Syntheses of (±)-Platensimycin and (±)-Platencin via a Dual-Mode Lewis Acid Induced Cascade Cyclization Approach J. Org. Chem. 2013, 78, 7912-7929 10.1021/jo401105q
-
(2013)
J. Org. Chem.
, vol.78
, pp. 7912-7929
-
-
Zhu, L.1
Zhou, C.2
Yang, W.3
He, S.4
Cheng, G.-J.5
Zhang, X.6
Lee, C.-S.7
-
370
-
-
84906951303
-
Total Synthesis of (-)-Platensimycin by Advancing Oxocarbenium- and Iminium-Mediated Catalytic Methods
-
Eey, S. T. C.; Lear, M. J. Total Synthesis of (-)-Platensimycin by Advancing Oxocarbenium- and Iminium-Mediated Catalytic Methods Chem.-Eur. J. 2014, 20, 11556-11573 10.1002/chem.201400131
-
(2014)
Chem. - Eur. J.
, vol.20
, pp. 11556-11573
-
-
Eey, S.T.C.1
Lear, M.J.2
-
371
-
-
78650333065
-
A Bismuth(III)-Catalyzed Friedel-Crafts Cyclization and Stereocontrolled Organocatalytic Approach to (-)-Platensimycin
-
Eey, S. T. C.; Lear, M. J. A Bismuth(III)-Catalyzed Friedel-Crafts Cyclization and Stereocontrolled Organocatalytic Approach to (-)-Platensimycin Org. Lett. 2010, 12, 5510-5513 10.1021/ol102390t
-
(2010)
Org. Lett.
, vol.12
, pp. 5510-5513
-
-
Eey, S.T.C.1
Lear, M.J.2
-
372
-
-
84946721764
-
Formal synthesis of (-)-platensimycin
-
Jiao, Z.-W.; Tu, Y.-Q.; Zhang, Q.; Liu, W.-X.; Wang, S.-H.; Wang, M. Formal synthesis of (-)-platensimycin Org. Chem. Front. 2015, 2, 913-916 10.1039/C5QO00109A
-
(2015)
Org. Chem. Front.
, vol.2
, pp. 913-916
-
-
Jiao, Z.-W.1
Tu, Y.-Q.2
Zhang, Q.3
Liu, W.-X.4
Wang, S.-H.5
Wang, M.6
-
373
-
-
84989494001
-
Radical cyclisation of dienes; Part IV. Enantiomerically pure building blocks from (R)-(-)- and (S)-(+)-carvone for the synthesis of naturally occurring triquinanes
-
Weinges, K.; Reichert, H. Radical cyclisation of dienes; part IV. Enantiomerically pure building blocks from (R)-(-)- and (S)-(+)-carvone for the synthesis of naturally occurring triquinanes Synlett 1991, 1991, 785-786 10.1055/s-1991-20874
-
(1991)
Synlett
, vol.1991
, pp. 785-786
-
-
Weinges, K.1
Reichert, H.2
-
374
-
-
0037087571
-
Oxidation of silyl enol ethers by using IBX and IBX•N-oxide complexes: A mild and selective reaction for the synthesis of enones
-
Nicolaou, K. C.; Gray, D. L. F.; Montagnon, T.; Harrison, S. T. Oxidation of silyl enol ethers by using IBX and IBX•N-oxide complexes: A mild and selective reaction for the synthesis of enones Angew. Chem., Int. Ed. 2002, 41, 996-1000 10.1002/1521-3773(20020315)41:6<996::AID-ANIE996>3.0.CO;2-I
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 996-1000
-
-
Nicolaou, K.C.1
Gray, D.L.F.2
Montagnon, T.3
Harrison, S.T.4
-
375
-
-
0035907919
-
Programming Organic Molecules: Design and Management of Organic Syntheses through Free-Radical Cascade Processes
-
McCarroll, A. J.; Walton, J. C. Programming Organic Molecules: Design and Management of Organic Syntheses through Free-Radical Cascade Processes Angew. Chem., Int. Ed. 2001, 40, 2224-2248 10.1002/1521-3773(20010618)40:12<2224::AID-ANIE2224>3.0.CO;2-F
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 2224-2248
-
-
McCarroll, A.J.1
Walton, J.C.2
-
376
-
-
33947094631
-
Unsaturated Carbenes
-
Stang, P. J. Unsaturated Carbenes Chem. Rev. 1978, 78, 383-405 10.1021/cr60314a003
-
(1978)
Chem. Rev.
, vol.78
, pp. 383-405
-
-
Stang, P.J.1
-
377
-
-
0001331380
-
-
4 th ed. Helmchen, G. Georg Thieme Verlag: New York
-
Taber, D. F. In Methods of Organic Chemistry, 4 th ed.; Helmchen, G., Ed.; Georg Thieme Verlag: New York, 1995; Vol. E21, p 1127.
-
(1995)
Methods of Organic Chemistry
, vol.21
, pp. 1127
-
-
Taber, D.F.1
-
378
-
-
0030739039
-
Alkenylidenes in Organic Synthesis
-
Kirmse, W. Alkenylidenes in Organic Synthesis Angew. Chem., Int. Ed. Engl. 1997, 36, 1164-1170 10.1002/anie.199711641
-
(1997)
Angew. Chem., Int. Ed. Engl.
, vol.36
, pp. 1164-1170
-
-
Kirmse, W.1
-
379
-
-
4644275985
-
Alkylidenecarbenes, Alkylidenecarbenoids, and Competing Species: Which Is Responsible for Vinylic Nucleophilic Substitution, [1 + 2] Cycloadditions, 1,5-CH Insertions, and the Fritsch-Buttenberg-Wiechell Rearrangement?
-
Knorr, R. Alkylidenecarbenes, Alkylidenecarbenoids, and Competing Species: Which Is Responsible for Vinylic Nucleophilic Substitution, [1 + 2] Cycloadditions, 1,5-CH Insertions, and the Fritsch-Buttenberg-Wiechell Rearrangement? Chem. Rev. 2004, 104, 3795-2850 10.1021/cr030616h
-
(2004)
Chem. Rev.
, vol.104
, pp. 2850-3795
-
-
Knorr, R.1
-
380
-
-
84862549632
-
Synthetic approaches toward sesterterpenoids
-
Hog, D. T.; Webster, R.; Trauner, D. Synthetic approaches toward sesterterpenoids Nat. Prod. Rep. 2012, 29, 752-779 10.1039/c2np20005h
-
(2012)
Nat. Prod. Rep.
, vol.29
, pp. 752-779
-
-
Hog, D.T.1
Webster, R.2
Trauner, D.3
-
381
-
-
77953659890
-
Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids
-
Luo, S.-H.; Luo, Q.; Niu, X.-M.; Xie, M.-J.; Zhao, X.; Schneider, B.; Gershenzon, J.; Li, S.-H. Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids Angew. Chem., Int. Ed. 2010, 49, 4471-4475 10.1002/anie.201000449
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 4471-4475
-
-
Luo, S.-H.1
Luo, Q.2
Niu, X.-M.3
Xie, M.-J.4
Zhao, X.5
Schneider, B.6
Gershenzon, J.7
Li, S.-H.8
-
382
-
-
84872304811
-
Asymmetric Total Synthesis of Leucosceptroid B
-
Huang, X.; Song, L.; Xu, J.; Zhu, G.; Liu, B. Asymmetric Total Synthesis of Leucosceptroid B Angew. Chem., Int. Ed. 2013, 52, 952-955 10.1002/anie.201208687
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 952-955
-
-
Huang, X.1
Song, L.2
Xu, J.3
Zhu, G.4
Liu, B.5
-
383
-
-
84907830975
-
A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)-Norleucosceptroid A, (-)-Norleucosceptroid B, and (-)-Leucosceptroid K
-
Hugelshofer, C. L.; Magauer, T. A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)-Norleucosceptroid A, (-)-Norleucosceptroid B, and (-)-Leucosceptroid K Angew. Chem., Int. Ed. 2014, 53, 11351-11355 10.1002/anie.201407788
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 11351-11355
-
-
Hugelshofer, C.L.1
Magauer, T.2
-
384
-
-
84926142255
-
Total Synthesis of the Leucosceptroid Family of Natural Products
-
Hugelshofer, C. L.; Magauer, T. Total Synthesis of the Leucosceptroid Family of Natural Products J. Am. Chem. Soc. 2015, 137, 3807-3810 10.1021/jacs.5b02021
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 3807-3810
-
-
Hugelshofer, C.L.1
Magauer, T.2
-
385
-
-
84921059023
-
Total Synthesis of Leucosceptroids A and B
-
Guo, S.; Liu, J.; Ma, D. Total Synthesis of Leucosceptroids A and B Angew. Chem., Int. Ed. 2015, 54, 1298-1301 10.1002/anie.201410134
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 1298-1301
-
-
Guo, S.1
Liu, J.2
Ma, D.3
-
386
-
-
84879542001
-
Enantioselective Intramolecular Aldehyde α- Alkylation with Simple Olefins: Direct Access to Homo-Ene Products
-
Comito, R. J.; Finelli, F. G.; MacMillan, D. W. C. Enantioselective Intramolecular Aldehyde α- Alkylation with Simple Olefins: Direct Access to Homo-Ene Products J. Am. Chem. Soc. 2013, 135, 9358-9361 10.1021/ja4047312
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 9358-9361
-
-
Comito, R.J.1
Finelli, F.G.2
MacMillan, D.W.C.3
-
387
-
-
81355138395
-
The intramolecular asymmetric allylation of aldehydes via organo-SOMO catalysis: A novel approach to ring construction
-
Pham, P. V.; Ashton, K.; MacMillan, D. W. C. The intramolecular asymmetric allylation of aldehydes via organo-SOMO catalysis: A novel approach to ring construction Chem. Sci. 2011, 2, 1470-1473 10.1039/c1sc00176k
-
(2011)
Chem. Sci.
, vol.2
, pp. 1470-1473
-
-
Pham, P.V.1
Ashton, K.2
MacMillan, D.W.C.3
-
388
-
-
0004653167
-
Chemical constituents of Gentianella alborosea (Gilg) Fabris
-
Senatore, F.; De Feo, V.; Zhou, Z. L. Chemical constituents of Gentianella alborosea (Gilg) Fabris Ann. Chim. 1991, 81, 269-274
-
(1991)
Ann. Chim.
, vol.81
, pp. 269-274
-
-
Senatore, F.1
De Feo, V.2
Zhou, Z.L.3
-
389
-
-
0030714178
-
Nitidasin, a novel sesterterpenoid, from the Peruvian folk medicine "hercampuri" (Gentianella nitida)
-
Kawahara, N.; Nozawa, M.; Flores, D.; Bonilla, P.; Sekita, S.; Satake, M.; Kawai, K.-I. Nitidasin, a novel sesterterpenoid, from the Peruvian folk medicine "Hercampuri" (Gentianella nitida) Chem. Pharm. Bull. 1997, 45, 1717-1719 10.1248/cpb.45.1717
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 1717-1719
-
-
Kawahara, N.1
Nozawa, M.2
Flores, D.3
Bonilla, P.4
Sekita, S.5
Satake, M.6
Kawai, K.-I.7
-
390
-
-
84905366449
-
The Total Synthesis of (-)-Nitidasin
-
Hog, D. T.; Huber, F. M. E.; Mayer, P.; Trauner, D. The Total Synthesis of (-)-Nitidasin Angew. Chem., Int. Ed. 2014, 53, 8513-8517 10.1002/anie.201403605
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 8513-8517
-
-
Hog, D.T.1
Huber, F.M.E.2
Mayer, P.3
Trauner, D.4
-
391
-
-
0026548831
-
Diastereoselective zirconocene-promoted bicyclization-carbonylation of allylically methyl-substituted enynes. Synthesis of (+)-iridomyrmecin
-
Agnel, G.; Owczarczyk, Z.; Negishi, E.-I. Diastereoselective zirconocene-promoted bicyclization-carbonylation of allylically methyl-substituted enynes. Synthesis of (+)-iridomyrmecin Tetrahedron Lett. 1992, 33, 1543-1546 10.1016/S0040-4039(00)91669-1
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 1543-1546
-
-
Agnel, G.1
Owczarczyk, Z.2
Negishi, E.-I.3
-
392
-
-
0000513376
-
Alkenylzinc-Mediated Approach to the Vitamin D Skeleton. Application to the Synthesis of 6-Methyl Analogs of Vitamin and Previtamin D
-
García, A. M.; Mascarenas, J. L.; Castedo, A.; Mourino, A. Alkenylzinc-Mediated Approach to the Vitamin D Skeleton. Application to the Synthesis of 6-Methyl Analogs of Vitamin and Previtamin D J. Org. Chem. 1997, 62, 6353-6358 10.1021/jo970605m
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6353-6358
-
-
García, A.M.1
Mascarenas, J.L.2
Castedo, A.3
Mourino, A.4
-
393
-
-
0002262097
-
(+)-(7aS)-7a-methyl-2,3,7,7a-tetrahydro-1 H-indene-1,5-(6H-Dione)
-
Hajos, Z. G.; Parrish, D. R. (+)-(7aS)-7a-methyl-2,3,7,7a-tetrahydro-1 H-indene-1,5-(6H-Dione) Org. Synth. 1985, 63, 26-31 10.15227/orgsyn.063.0026
-
(1985)
Org. Synth.
, vol.63
, pp. 26-31
-
-
Hajos, Z.G.1
Parrish, D.R.2
-
394
-
-
0016691895
-
Total syntheses of optically active 19-nor steroids. (+)-Estr-4-ene-3,17-dione and (+)-13β-ethylgon-4-ene-3,17-dione
-
Micheli, R. A.; Hojos, Z. G.; Cohen, N.; Parrish, D. R.; Portland, L. A.; Sciamanna, W.; Scott, M. A.; Wehrli, P. A. Total syntheses of optically active 19-nor steroids. (+)-Estr-4-ene-3,17-dione and (+)-13β-ethylgon-4-ene-3,17-dione J. Org. Chem. 1975, 40, 675-681 10.1021/jo00894a003
-
(1975)
J. Org. Chem.
, vol.40
, pp. 675-681
-
-
Micheli, R.A.1
Hojos, Z.G.2
Cohen, N.3
Parrish, D.R.4
Portland, L.A.5
Sciamanna, W.6
Scott, M.A.7
Wehrli, P.A.8
-
395
-
-
84863620825
-
A Unified Approach to trans-Hydrindane Sesterterpenoids
-
Hog, D. T.; Mayer, P.; Trauner, D. A Unified Approach to trans-Hydrindane Sesterterpenoids J. Org. Chem. 2012, 77, 5838-5843 10.1021/jo300726z
-
(2012)
J. Org. Chem.
, vol.77
, pp. 5838-5843
-
-
Hog, D.T.1
Mayer, P.2
Trauner, D.3
-
396
-
-
0034617006
-
The biology of ophiobolins
-
Au, T. K.; Chick, W. S.; Leung, P. C. The biology of ophiobolins Life Sci. 2000, 67, 733-742 10.1016/S0024-3205(00)00668-8
-
(2000)
Life Sci.
, vol.67
, pp. 733-742
-
-
Au, T.K.1
Chick, W.S.2
Leung, P.C.3
-
397
-
-
84875907848
-
Ophiobolin A induces paraptosis-like cell death in human glioblastoma cells by decreasing BKCa channel activity
-
Bury, M.; Girault, G.; Mégalizzi, V.; Spiegl-Kreinecker, S.; Mathieu, V.; Berger, W.; Evidente, A.; Kornienko, A.; Gailly, P.; Vandier, C. et al. Ophiobolin A induces paraptosis-like cell death in human glioblastoma cells by decreasing BKCa channel activity Cell Death Dis. 2013, 4, e561 10.1038/cddis.2013.85
-
(2013)
Cell Death Dis.
, vol.4
, pp. e561
-
-
Bury, M.1
Girault, G.2
Mégalizzi, V.3
Spiegl-Kreinecker, S.4
Mathieu, V.5
Berger, W.6
Evidente, A.7
Kornienko, A.8
Gailly, P.9
Vandier, C.10
-
398
-
-
0000431466
-
Total synthesis of (+)-ophiobolin C
-
Rowley, M.; Tsukamoto, M.; Kishi, Y. Total synthesis of (+)-ophiobolin C J. Am. Chem. Soc. 1989, 111, 2735-2737 10.1021/ja00189a069
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 2735-2737
-
-
Rowley, M.1
Tsukamoto, M.2
Kishi, Y.3
-
399
-
-
80053169701
-
Convergent Total Synthesis of (+)-Opiobolin A
-
Tsuna, K.; Noguchi, N.; Nakada, M. Convergent Total Synthesis of (+)-Opiobolin A Angew. Chem., Int. Ed. 2011, 50, 9452-9455 10.1002/anie.201104447
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 9452-9455
-
-
Tsuna, K.1
Noguchi, N.2
Nakada, M.3
-
400
-
-
84876217697
-
Enantioselective Total Synthesis of (+)-Ophiobolin A
-
Tsuna, K.; Noguchi, N.; Nakada, M. Enantioselective Total Synthesis of (+)-Ophiobolin A Chem.-Eur. J. 2013, 19, 5476-5486 10.1002/chem.201204119
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 5476-5486
-
-
Tsuna, K.1
Noguchi, N.2
Nakada, M.3
-
401
-
-
84971508913
-
Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade
-
Brill, Z. G.; Grover, H. K.; Maimone, T. J. Enantioselective synthesis of an ophiobolin sesterterpene via a programmed radical cascade Science 2016, 352, 1078-1082 10.1126/science.aaf6742
-
(2016)
Science
, vol.352
, pp. 1078-1082
-
-
Brill, Z.G.1
Grover, H.K.2
Maimone, T.J.3
-
402
-
-
0032567221
-
Enantioselective Cyclopropanation of Allylic Alcohols with Dioxaborolane Ligands: Scope and Synthetic Applications
-
Charette, A. B.; Juteau, H.; Lebel, H.; Molinaro, C. Enantioselective Cyclopropanation of Allylic Alcohols with Dioxaborolane Ligands: Scope and Synthetic Applications J. Am. Chem. Soc. 1998, 120, 11943-11952 10.1021/ja982055v
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 11943-11952
-
-
Charette, A.B.1
Juteau, H.2
Lebel, H.3
Molinaro, C.4
-
403
-
-
0033484573
-
Polarity-reversal catalysis of hydrogen-atom abstraction reactions: Concepts and applications in organic chemistry
-
Roberts, B. P. Polarity-reversal catalysis of hydrogen-atom abstraction reactions: Concepts and applications in organic chemistry Chem. Soc. Rev. 1999, 28, 25-35 10.1039/a804291h
-
(1999)
Chem. Soc. Rev.
, vol.28
, pp. 25-35
-
-
Roberts, B.P.1
-
404
-
-
0036015090
-
Carbohydrate-derived thiols as protic polarity-reversal catalysts for enantioselective radical-chain reactions
-
Cai, Y.; Roberts, B. P.; Tocher, D. A. Carbohydrate-derived thiols as protic polarity-reversal catalysts for enantioselective radical-chain reactions J. Chem. Soc. Perkin Trans. 1 2002, 1376-1386 10.1039/b202022j
-
(2002)
J. Chem. Soc. Perkin Trans. 1
, pp. 1376-1386
-
-
Cai, Y.1
Roberts, B.P.2
Tocher, D.A.3
-
405
-
-
79952026605
-
Synthesis, biology and clinical significance of pentacyclic triterpenes: A multi-target approach to prevention and treatment of metabolic and vascular diseases
-
Sheng, H.; Sun, H. Synthesis, biology and clinical significance of pentacyclic triterpenes: a multi-target approach to prevention and treatment of metabolic and vascular diseases Nat. Prod. Rep. 2011, 28, 543-593 10.1039/c0np00059k
-
(2011)
Nat. Prod. Rep.
, vol.28
, pp. 543-593
-
-
Sheng, H.1
Sun, H.2
-
406
-
-
49949129079
-
Sur l'origine triterpenique des constituants amers des simarubacees
-
Moron, J.; Polonsky, J. Sur l'origine triterpenique des constituants amers des simarubacees Tetrahedron Lett. 1968, 9, 385-390 10.1016/S0040-4039(01)98767-2
-
(1968)
Tetrahedron Lett.
, vol.9
, pp. 385-390
-
-
Moron, J.1
Polonsky, J.2
-
407
-
-
49649159572
-
Sur la biosynthèse des quassinoïdes de Simaruba glauca (Simarubaceae)
-
Moron, J.; Merrien, M.-A.; Polonsky, J. Sur la biosynthèse des quassinoïdes de Simaruba glauca (Simarubaceae) Phytochemistry 1971, 10, 585-592 10.1016/S0031-9422(00)94702-2
-
(1971)
Phytochemistry
, vol.10
, pp. 585-592
-
-
Moron, J.1
Merrien, M.-A.2
Polonsky, J.3
-
408
-
-
11844255707
-
Biologically active quassinoids and their chemistry: Potential leads for drug design
-
Guo, Z.; Vangapandu, S.; Sindelar, R. W.; Walker, L. A.; Sindelar, R. D. Biologically active quassinoids and their chemistry: Potential leads for drug design Curr. Med. Chem. 2005, 12, 173-190 10.2174/0929867053363351
-
(2005)
Curr. Med. Chem.
, vol.12
, pp. 173-190
-
-
Guo, Z.1
Vangapandu, S.2
Sindelar, R.W.3
Walker, L.A.4
Sindelar, R.D.5
-
409
-
-
79251517716
-
Quassinoids: From traditional drugs to new cancer therapeutics
-
Fiaschetti, G.; Grotzer, M. A.; Shalaby, T.; Castelletti, D.; Arcaro, A. Quassinoids: From traditional drugs to new cancer therapeutics Curr. Med. Chem. 2011, 18, 316-328 10.2174/092986711794839205
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 316-328
-
-
Fiaschetti, G.1
Grotzer, M.A.2
Shalaby, T.3
Castelletti, D.4
Arcaro, A.5
-
410
-
-
84952743011
-
Synthesis of quassinoids: A review
-
Kawada, K.; Kim, M.; Watt, D. S. Synthesis of quassinoids: A review Org. Prep. Proced. Int. 1989, 21, 521-618 10.1080/00304948909356425
-
(1989)
Org. Prep. Proced. Int.
, vol.21
, pp. 521-618
-
-
Kawada, K.1
Kim, M.2
Watt, D.S.3
-
411
-
-
44349148803
-
Quassinoids: Structural diversity, biological activity and synthetic studies
-
Curcino Vieira, I. J.; Braz-Filho, R. Quassinoids: Structural diversity, biological activity and synthetic studies Stud. Nat. Prod. Chem. 2006, 33, 433-492 10.1016/S1572-5995(06)80032-3
-
(2006)
Stud. Nat. Prod. Chem.
, vol.33
, pp. 433-492
-
-
Curcino Vieira, I.J.1
Braz-Filho, R.2
-
412
-
-
0034693180
-
Total Synthesis of (+)-quassin
-
Shing, T. K. M.; Jiang, Q. Total Synthesis of (+)-quassin J. Org. Chem. 2000, 65, 7059-7069 10.1021/jo000877g
-
(2000)
J. Org. Chem.
, vol.65
, pp. 7059-7069
-
-
Shing, T.K.M.1
Jiang, Q.2
-
413
-
-
29144498430
-
Total Synthesis of (-)-Samaderine y from (S)-(+)-carvone
-
Shing, T. K. M.; Yeung, Y. Y. Total Synthesis of (-)-Samaderine Y from (S)-(+)-carvone Angew. Chem., Int. Ed. 2005, 44, 7981-7984 10.1002/anie.200502763
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 7981-7984
-
-
Shing, T.K.M.1
Yeung, Y.Y.2
-
414
-
-
0029867976
-
Synthetic studies towards pentacyclic quassinoids: Facile and stereocontrolled construction of the e ring
-
Shing, T. K. M.; Zhu, X. Y.; Mak, T. C. W. Synthetic studies towards pentacyclic quassinoids: Facile and stereocontrolled construction of the E ring Tetrahedron: Asymmetry 1996, 7, 673-676 10.1016/0957-4166(96)00062-6
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 673-676
-
-
Shing, T.K.M.1
Zhu, X.Y.2
Mak, T.C.W.3
-
415
-
-
0002613329
-
[1,3]-sigmatropic shifts of alkoxides
-
Wilson, S. R.; Mao, D. T.; Jernberg, K. M.; Ezmirly, S. T. [1,3]-sigmatropic shifts of alkoxides Tetrahedron Lett. 1977, 18, 2559-2562 10.1016/S0040-4039(01)83819-3
-
(1977)
Tetrahedron Lett.
, vol.18
, pp. 2559-2562
-
-
Wilson, S.R.1
Mao, D.T.2
Jernberg, K.M.3
Ezmirly, S.T.4
-
416
-
-
17344367543
-
Thermal [1,j] sigmatropic rearrangements
-
Spangler, C. W. Thermal [1,j] sigmatropic rearrangements Chem. Rev. 1976, 76, 187-217 10.1021/cr60300a002
-
(1976)
Chem. Rev.
, vol.76
, pp. 187-217
-
-
Spangler, C.W.1
-
417
-
-
79960911912
-
Diastereoselective Total Synthesis of (±)-Schindilactone A
-
Xiao, Q.; Ren, W.-W.; Chen, Z.-X.; Sun, T.-W.; Li, Y.; Ye, Q.-D.; Gong, J.-X.; Meng, F.-K.; You, L.; Liu, Y.-F. et al. Diastereoselective Total Synthesis of (±)-Schindilactone A Angew. Chem., Int. Ed. 2011, 50, 7373-7377 10.1002/anie.201103088
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7373-7377
-
-
Xiao, Q.1
Ren, W.-W.2
Chen, Z.-X.3
Sun, T.-W.4
Li, Y.5
Ye, Q.-D.6
Gong, J.-X.7
Meng, F.-K.8
You, L.9
Liu, Y.-F.10
-
418
-
-
84914129269
-
Total Synthesis of Rubriflordilactone A
-
Li, J.; Yang, P.; Yao, M.; Deng, J.; Li, A. Total Synthesis of Rubriflordilactone A J. Am. Chem. Soc. 2014, 136, 16477-16480 10.1021/ja5092563
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 16477-16480
-
-
Li, J.1
Yang, P.2
Yao, M.3
Deng, J.4
Li, A.5
-
419
-
-
84929460337
-
Total Synthesis of Schilancitrilactones B and C
-
Wang, L.; Wang, H.; Li, Y.; Tang, P. Total Synthesis of Schilancitrilactones B and C Angew. Chem., Int. Ed. 2015, 54, 5732-5735 10.1002/anie.201501169
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 5732-5735
-
-
Wang, L.1
Wang, H.2
Li, Y.3
Tang, P.4
-
420
-
-
84939779150
-
Asymmetric Total Synthesis of Propindilactone G
-
You, L.; Liang, X.-T.; Xu, L.-M.; Wang, Y.-F.; Zhang, J.-J.; Su, Q.; Li, Y.-H.; Zhang, B.; Yang, S.-L.; Chen, J.-H. et al. Asymmetric Total Synthesis of Propindilactone G J. Am. Chem. Soc. 2015, 137, 10120-10123 10.1021/jacs.5b06480
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 10120-10123
-
-
You, L.1
Liang, X.-T.2
Xu, L.-M.3
Wang, Y.-F.4
Zhang, J.-J.5
Su, Q.6
Li, Y.-H.7
Zhang, B.8
Yang, S.-L.9
Chen, J.-H.10
-
421
-
-
84944239873
-
Total Synthesis of (+)-Rubriflordilactone A
-
Goh, S.-S.; Chaubet, G.; Gockel, B.; Cordonnier, M.-C. A.; Baars, H.; Phillips, A. W.; Anderson, E. A. Total Synthesis of (+)-Rubriflordilactone A Angew. Chem., Int. Ed. 2015, 54, 12618-12621 10.1002/anie.201506366
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 12618-12621
-
-
Goh, S.-S.1
Chaubet, G.2
Gockel, B.3
Cordonnier, M.-C.A.4
Baars, H.5
Phillips, A.W.6
Anderson, E.A.7
-
422
-
-
84973139122
-
Total Synthesis of Rubriflordilactone B
-
Yang, P.; Yao, M.; Li, J.; Li, Y.; Li, A. Total Synthesis of Rubriflordilactone B Angew. Chem., Int. Ed. 2016, 55, 6964-6968 10.1002/anie.201601915
-
(2016)
Angew. Chem., Int. Ed.
, vol.55
, pp. 6964-6968
-
-
Yang, P.1
Yao, M.2
Li, J.3
Li, Y.4
Li, A.5
-
423
-
-
52649111043
-
Triterpenoids from the Schisandraceae family
-
Xiao, W.-L.; Li, R.-T.; Huang, S.-X.; Pu, J.-X.; Sun, H.-D. Triterpenoids from the Schisandraceae family Nat. Prod. Rep. 2008, 25, 871-891 10.1039/b719905h
-
(2008)
Nat. Prod. Rep.
, vol.25
, pp. 871-891
-
-
Xiao, W.-L.1
Li, R.-T.2
Huang, S.-X.3
Pu, J.-X.4
Sun, H.-D.5
-
424
-
-
84924431751
-
Triterpenoids from the Schisandraceae family: An update
-
Shi, Y.-M.; Xiao, W.-L.; Pu, J.-X.; Sun, H. D. Triterpenoids from the Schisandraceae family: An update Nat. Prod. Rep. 2015, 32, 367-410 10.1039/C4NP00117F
-
(2015)
Nat. Prod. Rep.
, vol.32
, pp. 367-410
-
-
Shi, Y.-M.1
Xiao, W.-L.2
Pu, J.-X.3
Sun, H.D.4
-
425
-
-
33644963538
-
Rubriflordilactones A and B, Two Novel Bisnortriterpenoids from Schisandra rubriflora and Their Biological Activities
-
Xiao, W.-L.; Yang, L.-M.; Gong, N.-B.; Wu, L.; Wang, R.-R.; Pu, J.-X.; Li, X.-L.; Huang, S.-X.; Zheng, Y.-T.; Li, R.-T. et al. Rubriflordilactones A and B, Two Novel Bisnortriterpenoids from Schisandra rubriflora and Their Biological Activities Org. Lett. 2006, 8, 991-994 10.1021/ol060062f
-
(2006)
Org. Lett.
, vol.8
, pp. 991-994
-
-
Xiao, W.-L.1
Yang, L.-M.2
Gong, N.-B.3
Wu, L.4
Wang, R.-R.5
Pu, J.-X.6
Li, X.-L.7
Huang, S.-X.8
Zheng, Y.-T.9
Li, R.-T.10
-
426
-
-
85011245852
-
Scandium Trifluoromethanesulfonate as an Extremely Active Acylation Catalyst
-
Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H. Scandium Trifluoromethanesulfonate as an Extremely Active Acylation Catalyst J. Am. Chem. Soc. 1995, 117, 4413-4414 10.1021/ja00120a030
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 4413-4414
-
-
Ishihara, K.1
Kubota, M.2
Kurihara, H.3
Yamamoto, H.4
-
427
-
-
84881117009
-
Total synthesis of the Daphniphyllum alkaloid daphenylline
-
Lu, Z.; Li, Y.; Deng, J.; Li, A. Total synthesis of the Daphniphyllum alkaloid daphenylline Nat. Chem. 2013, 5, 679-684 10.1038/nchem.1694
-
(2013)
Nat. Chem.
, vol.5
, pp. 679-684
-
-
Lu, Z.1
Li, Y.2
Deng, J.3
Li, A.4
-
428
-
-
84924794981
-
Total synthesis of clostrubin
-
Yang, M.; Li, J.; Li, A. Total synthesis of clostrubin Nat. Commun. 2015, 6, 6445 10.1038/ncomms7445
-
(2015)
Nat. Commun.
, vol.6
, pp. 6445
-
-
Yang, M.1
Li, J.2
Li, A.3
-
429
-
-
85006314785
-
Computational Chemistry Driven Solution to Rubriflordilactone B
-
Grimblat, N.; Kaufman, T. S.; Sarotti, A. M. Computational Chemistry Driven Solution to Rubriflordilactone B Org. Lett. 2016, 18, 6420-6423 10.1021/acs.orglett.6b03318
-
(2016)
Org. Lett.
, vol.18
, pp. 6420-6423
-
-
Grimblat, N.1
Kaufman, T.S.2
Sarotti, A.M.3
-
430
-
-
84863281880
-
Schilancitrilactones A-C: Three Unique Nortriterpenoids from Schisandra lancifolia
-
Luo, X.; Shi, Y.-M.; Luo, R.-H.; Luo, S.-H.; Li, X.-N.; Wang, R.-R.; Li, S.-H.; Zheng, Y.-T.; Du, X.; Xiao, W.-L. et al. Schilancitrilactones A-C: Three Unique Nortriterpenoids from Schisandra lancifolia Org. Lett. 2012, 14, 1286-1289 10.1021/ol300099e
-
(2012)
Org. Lett.
, vol.14
, pp. 1286-1289
-
-
Luo, X.1
Shi, Y.-M.2
Luo, R.-H.3
Luo, S.-H.4
Li, X.-N.5
Wang, R.-R.6
Li, S.-H.7
Zheng, Y.-T.8
Du, X.9
Xiao, W.-L.10
-
431
-
-
0000852344
-
Stereoselective synthesis of cis-decalins via Diels-Alder and double Michael addition of substituted Nazarov reagents
-
Lavallée, J.-F.; Spino, C.; Ruel, R.; Hogan, T. K.; Deslongchamps, P. Stereoselective synthesis of cis-decalins via Diels-Alder and double Michael addition of substituted Nazarov reagents Can. J. Chem. 1992, 70, 1406-1426 10.1139/v92-179
-
(1992)
Can. J. Chem.
, vol.70
, pp. 1406-1426
-
-
Lavallée, J.-F.1
Spino, C.2
Ruel, R.3
Hogan, T.K.4
Deslongchamps, P.5
-
432
-
-
0000727176
-
Ultrasound in organic synthesis 16. Optimisation of the conjugate additions to α,β-unsaturated carbonyl compounds in aqueous media
-
Luche, J. L.; Allavena, C. Ultrasound in organic synthesis 16. Optimisation of the conjugate additions to α,β-unsaturated carbonyl compounds in aqueous media Tetrahedron Lett. 1988, 29, 5369-5372 10.1016/S0040-4039(00)82870-1
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 5369-5372
-
-
Luche, J.L.1
Allavena, C.2
-
433
-
-
52449097167
-
Synthesis of 5-(bromomethylene)furan-2-(5H)-ones and 3-(bromomethylene)isobenzofuran-1(3H)-ones as inhibitors of microbial quorum sensing
-
Benneche, T.; Hussain, Z.; Aamdal Scheie, A.; Lonn-Stensrud, J. Synthesis of 5-(bromomethylene)furan-2-(5H)-ones and 3-(bromomethylene)isobenzofuran-1(3H)-ones as inhibitors of microbial quorum sensing New J. Chem. 2008, 32, 1567-1572 10.1039/b803926g
-
(2008)
New J. Chem.
, vol.32
, pp. 1567-1572
-
-
Benneche, T.1
Hussain, Z.2
Aamdal Scheie, A.3
Lonn-Stensrud, J.4
-
434
-
-
84935029826
-
Current complexity: A tool for assessing the complexity of organic molecules
-
Li, J.; Eastgate, M. D. Current complexity: a tool for assessing the complexity of organic molecules Org. Biomol. Chem. 2015, 13, 7164-7176 10.1039/C5OB00709G
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 7164-7176
-
-
Li, J.1
Eastgate, M.D.2
-
435
-
-
77954562085
-
Aiming for the Ideal Synthesis
-
Gaich, T.; Baran, P. S. Aiming for the Ideal Synthesis J. Org. Chem. 2010, 75, 4657-4673 10.1021/jo1006812
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4657-4673
-
-
Gaich, T.1
Baran, P.S.2
-
436
-
-
17244375099
-
A Convergent Enantioselective Route to Structurally Diverse 6-Deoxytetracycline Antibiotics
-
Charest, M. G.; Lerner, C. D.; Brubaker, J. D.; Siegel, D. R.; Myers, A. G. A Convergent Enantioselective Route to Structurally Diverse 6-Deoxytetracycline Antibiotics Science 2005, 308, 395-398 10.1126/science.1109755
-
(2005)
Science
, vol.308
, pp. 395-398
-
-
Charest, M.G.1
Lerner, C.D.2
Brubaker, J.D.3
Siegel, D.R.4
Myers, A.G.5
-
437
-
-
84970948129
-
A Platform for the Discovery of New Macrolide Antibiotics
-
Seiple, I. B.; Zhang, Z.; Jakubec, P.; Langlois-Mercier, A.; Wright, P. M.; Hog, D. T.; Yabu, K.; Allu, S. R.; Fukuzaki, T.; Carlsen, P. N. et al. A Platform for the Discovery of New Macrolide Antibiotics Nature 2016, 533, 338-345 10.1038/nature17967
-
(2016)
Nature
, vol.533
, pp. 338-345
-
-
Seiple, I.B.1
Zhang, Z.2
Jakubec, P.3
Langlois-Mercier, A.4
Wright, P.M.5
Hog, D.T.6
Yabu, K.7
Allu, S.R.8
Fukuzaki, T.9
Carlsen, P.N.10
-
438
-
-
84989227776
-
Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin
-
Feng, J.; Noack, F.; Krische, M. J. Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin J. Am. Chem. Soc. 2016, 138, 12364-12367 10.1021/jacs.6b08902
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 12364-12367
-
-
Feng, J.1
Noack, F.2
Krische, M.J.3
-
439
-
-
84941130834
-
Discovery of Novel Synthetic Methodologies and Reagents during Natural Product Synthesis in the Post-Palytoxin Era
-
Armaly, A. M.; DePorre, Y. C.; Groso, E. J.; Riehl, P. S.; Schindler, C. S. Discovery of Novel Synthetic Methodologies and Reagents during Natural Product Synthesis in the Post-Palytoxin Era Chem. Rev. 2015, 115, 9232-9276 10.1021/acs.chemrev.5b00034
-
(2015)
Chem. Rev.
, vol.115
, pp. 9232-9276
-
-
Armaly, A.M.1
DePorre, Y.C.2
Groso, E.J.3
Riehl, P.S.4
Schindler, C.S.5
-
440
-
-
84934908603
-
-
Ed. Topics in Current Chemistry 346; Springer: Berlin
-
C-C Bond Activation; Dong, G., Ed.; Topics in Current Chemistry 346; Springer: Berlin, 2014.
-
(2014)
C-C Bond Activation
-
-
Dong, G.1
-
441
-
-
0002583629
-
Cleavage of Carbon-Carbon Single Bonds by Transition Metals
-
Murai, S. Springer: Berlin
-
Murakami, M.; Ito, Y. Cleavage of Carbon-Carbon Single Bonds by Transition Metals. In Topics in Organometallic Chemistry; Murai, S., Ed.; Springer: Berlin, 1999; Vol. 3, p 97.
-
(1999)
Topics in Organometallic Chemistry
, vol.3
, pp. 97
-
-
Murakami, M.1
Ito, Y.2
-
442
-
-
0033119285
-
Metal Insertion into C-C Bonds in Solution
-
Rybtchinski, B.; Milstein, D. Metal Insertion into C-C Bonds in Solution Angew. Chem., Int. Ed. 1999, 38, 870-883 10.1002/(SICI)1521-3773(19990401)38:7<870::AID-ANIE870>3.0.CO;2-3
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 870-883
-
-
Rybtchinski, B.1
Milstein, D.2
-
443
-
-
11844273927
-
Transition metal-catalyzed carbon-carbon bond activation
-
Jun, C. H. Transition metal-catalyzed carbon-carbon bond activation Chem. Soc. Rev. 2004, 33, 610-618 10.1039/B308864M
-
(2004)
Chem. Soc. Rev.
, vol.33
, pp. 610-618
-
-
Jun, C.H.1
-
444
-
-
84930225615
-
Selective C-C and C-H Bond Activation/Cleavage of Pinene Derivatives: Synthesis of Enantiopure Cyclohexenone Scaffolds and Mechanistic Insights
-
Masarwa, A.; Weber, M.; Sarpong, R. Selective C-C and C-H Bond Activation/Cleavage of Pinene Derivatives: Synthesis of Enantiopure Cyclohexenone Scaffolds and Mechanistic Insights J. Am. Chem. Soc. 2015, 137, 6327-6334 10.1021/jacs.5b02254
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 6327-6334
-
-
Masarwa, A.1
Weber, M.2
Sarpong, R.3
-
445
-
-
84946781054
-
Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction
-
Weber, M.; Owens, K.; Masarwa, A.; Sarpong, R. Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction Org. Lett. 2015, 17, 5432-5435 10.1021/acs.orglett.5b02797
-
(2015)
Org. Lett.
, vol.17
, pp. 5432-5435
-
-
Weber, M.1
Owens, K.2
Masarwa, A.3
Sarpong, R.4
-
446
-
-
85008319081
-
Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin
-
Hung, K.; Condakes, M. L.; Morikawa, T.; Maimone, T. J. Oxidative Entry into the Illicium Sesquiterpenes: Enantiospecific Synthesis of (+)-Pseudoanisatin J. Am. Chem. Soc. 2016, 138, 16616-16619 10.1021/jacs.6b11739
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 16616-16619
-
-
Hung, K.1
Condakes, M.L.2
Morikawa, T.3
Maimone, T.J.4
-
447
-
-
0034686072
-
Recent Advances in the Pauson-Khand Reaction and Related [2+2+1] Cycloadditions
-
Brummond, K. M.; Kent, J. L. Recent Advances in the Pauson-Khand Reaction and Related [2+2+1] Cycloadditions Tetrahedron 2000, 56, 3263-3283 10.1016/S0040-4020(00)00148-4
-
(2000)
Tetrahedron
, vol.56
, pp. 3263-3283
-
-
Brummond, K.M.1
Kent, J.L.2
-
448
-
-
84890069342
-
Natural Products as Starting Points for the Synthesis of Complex and Diverse Compounds
-
Morrison, K. C.; Hergenrother, P. Natural Products as Starting Points for the Synthesis of Complex and Diverse Compounds Nat. Prod. Rep. 2014, 31, 6 10.1039/C3NP70063A
-
(2014)
Nat. Prod. Rep.
, vol.31
, pp. 6
-
-
Morrison, K.C.1
Hergenrother, P.2
-
449
-
-
79952683877
-
Enzymatic Functionalization of Carbon-hydrogen Bonds
-
Lewis, J. C.; Coelho, P. S.; Arnold, F. H. Enzymatic Functionalization of Carbon-hydrogen Bonds Chem. Soc. Rev. 2011, 40, 2003-2021 10.1039/C0CS00067A
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 2003-2021
-
-
Lewis, J.C.1
Coelho, P.S.2
Arnold, F.H.3
-
450
-
-
84859565523
-
Tuning P450 Enzymes as Oxidation Catalysts
-
Fasan, R. Tuning P450 Enzymes as Oxidation Catalysts ACS Catal. 2012, 2, 647-666 10.1021/cs300001x
-
(2012)
ACS Catal.
, vol.2
, pp. 647-666
-
-
Fasan, R.1
-
451
-
-
84863466093
-
Achieving regio- and enantioselectivity of P450-catalyzed oxidative C-H activation of small functionalized molecules by structure-guided directed evolution
-
Agudo, R.; Roiban, G. D.; Reetz, M. T. Achieving regio- and enantioselectivity of P450-catalyzed oxidative C-H activation of small functionalized molecules by structure-guided directed evolution ChemBioChem 2012, 13, 1465-1473 10.1002/cbic.201200244
-
(2012)
ChemBioChem
, vol.13
, pp. 1465-1473
-
-
Agudo, R.1
Roiban, G.D.2
Reetz, M.T.3
|