-
2
-
-
12344273765
-
Effect of enzymatic aroma release on the volatile compounds of white wines presenting different aroma potentials
-
Rocha, S. M.; Coutinho, P.; Delgadillo, I.; Dias Cardoso, A.; Coimbra, M. A. Effect of enzymatic aroma release on the volatile compounds of white wines presenting different aroma potentials. J. Sci. Food. Agric. 2005, 85, 199-205.
-
(2005)
J. Sci. Food. Agric
, vol.85
, pp. 199-205
-
-
Rocha, S.M.1
Coutinho, P.2
Delgadillo, I.3
Dias Cardoso, A.4
Coimbra, M.A.5
-
3
-
-
80052571022
-
Synthesis and biological evaluation of α,β-unsaturated lactones as potent immunosuppressive agents
-
2012, 22, 1287
-
Lee, S.-M.; Lee, W.-G.; Kim, Y.-C.; Ko, H. Synthesis and biological evaluation of α,β-unsaturated lactones as potent immunosuppressive agents. Bioorg. Med. Chem. Lett. 2011, 21, 5726-5729; 2012, 22, 1287
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 5726-5729
-
-
Lee, S.-M.1
Lee, W.-G.2
Kim, Y.-C.3
Ko, H.4
-
4
-
-
33644961939
-
Synthesis and biological properties of new α-methylene-γ-butyrolactones and α,β- unsaturated-δ-lactones
-
Cateni, F.; Zilic, J.; Zacchigna, M.; Bonivento, P.; Frausin, F.; Scarcia, V. Synthesis and biological properties of new α-methylene-γ-butyrolactones and α,β- unsaturated-δ-lactones. Eur. J. Med. Chem. 2006, 41, 192-200
-
(2006)
Eur. J. Med. Chem
, vol.41
, pp. 192-200
-
-
Cateni, F.1
Zilic, J.2
Zacchigna, M.3
Bonivento, P.4
Frausin, F.5
Scarcia, V.6
-
5
-
-
33845370152
-
Styryl lactones and their derivatives: Biological activities, mechanisms of action and potential leads for drug design
-
de Fátima, A.; Modolo, L. V.; Conegero, L. S.; Pilli, R. A.; Ferreira, C. V.; Kohn, L. K.; de Carvalho, J. Styryl lactones and their derivatives: biological activities, mechanisms of action and potential leads for drug design. Curr. Med. Chem. 2006, 13, 3371-3384
-
(2006)
Curr. Med. Chem
, vol.13
, pp. 3371-3384
-
-
de Fátima, A.1
Modolo, L.V.2
Conegero, L.S.3
Pilli, R.A.4
Ferreira, C.V.5
Kohn, L.K.6
de Carvalho, J.7
-
7
-
-
33847799053
-
Recent advances in the chemistry of unsaturated lactones
-
For early accounts on classical synthetic methods, see
-
For early accounts on classical synthetic methods, see: (a) Rao, Y. S. Recent advances in the chemistry of unsaturated lactones. Chem. Rev. 1976, 76, 625-694
-
(1976)
Chem. Rev
, vol.76
, pp. 625-694
-
-
Rao, Y.S.1
-
8
-
-
0003855123
-
-
S. Patai, Z. Rappoport Eds.; Wiley & Sons: Chichester, UK, Selected examples of non metathetic approaches
-
Ogliaruso, M. A.; Wolfe, J. F. Synthesis of Lactones and Lactams (The Chemistry of Functional Groups); S. Patai, Z. Rappoport Eds.; Wiley & Sons: Chichester, UK, 1993. Selected examples of non metathetic approaches
-
(1993)
Synthesis of Lactones and Lactams (The Chemistry of Functional Groups)
-
-
Ogliaruso, M.A.1
Wolfe, J.F.2
-
9
-
-
0028232231
-
Unsaturated lactones: Synthesis and applications
-
Yu, H.; Kayser, M. M. Unsaturated lactones: synthesis and applications. Synth. Commun. 1994, 24, 1583-1588
-
(1994)
Synth. Commun
, vol.24
, pp. 1583-1588
-
-
Yu, H.1
Kayser, M.M.2
-
10
-
-
0000510920
-
Ruthenium-catalyzed synthesis of butenolides and pentenolides via contra-electronic α-alkylation of hydroxyalkynoates
-
Trost, B. M.; Müller, T. J. J.; Martinez, J. Ruthenium-catalyzed synthesis of butenolides and pentenolides via contra-electronic α-alkylation of hydroxyalkynoates. J. Am. Chem. Soc. 1995, 117, 1888-1899
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 1888-1899
-
-
Trost, B.M.1
Müller, T.J.J.2
Martinez, J.3
-
11
-
-
0033549671
-
A versatile preparation of α,β-unsaturated Lactones from homoallylic alcohols
-
Keck, G. E.; Li, X.-Y.; Knutson, C. E. A versatile preparation of α,β-unsaturated Lactones from homoallylic alcohols. Org. Lett. 1999, 1, 411-413.
-
(1999)
Org. Lett
, vol.1
, pp. 411-413
-
-
Keck, G.E.1
Li, X.-Y.2
Knutson, C.E.3
-
12
-
-
0344006321
-
Olefin metathesis and beyond
-
: (a) Fürstner, A. Olefin metathesis and beyond. Angew. Chem. Int. Ed. 2000, 39, 3012-3043
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 3012-3043
-
-
Fürstner, A.1
-
13
-
-
0034746687
-
The development of L2X2Ru=CHR olefin metathesis catalysts: An organometallic success story
-
Trnka, T. M.; Grubbs, R. H. The development of L2X2Ru=CHR olefin metathesis catalysts: an organometallic success story. Acc. Chem. Res. 2001, 34, 18-29
-
(2001)
Acc. Chem. Res
, vol.34
, pp. 18-29
-
-
Trnka, T.M.1
Grubbs, R.H.2
-
14
-
-
0035793845
-
Catalytic asymmetric olefin metathesis
-
Hoveyda, A. H.; Schrock, R. R. Catalytic asymmetric olefin metathesis. Chem. Eur. J. 2001, 7, 945-950
-
(2001)
Chem. Eur. J
, vol.7
, pp. 945-950
-
-
Hoveyda, A.H.1
Schrock, R.R.2
-
15
-
-
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
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 4490-4527
-
-
Nicolaou, K.C.1
Bulger, P.G.2
Sarlah, D.3
-
16
-
-
77954897138
-
Chemoselective olefin metathesis transformations mediated by ruthenium complexes
-
Nolan, S. P.; Clavier, H. Chemoselective olefin metathesis transformations mediated by ruthenium complexes. Chem. Soc. Rev. 2010, 39, 3305-3316.
-
(2010)
Chem. Soc. Rev
, vol.39
, pp. 3305-3316
-
-
Nolan, S.P.1
Clavier, H.2
-
17
-
-
79955869493
-
Stereoselective synthesis of five biologically active, naturally occurring medium and large ring lactones
-
Reviews
-
Reviews: (a) Marco, J. A.; Carda, M. Stereoselective synthesis of five biologically active, naturally occurring medium and large ring lactones. Nat. Prod. Commun. 2011, 6, 505-514
-
(2011)
Nat. Prod. Commun
, vol.6
, pp. 505-514
-
-
Marco, J.A.1
Carda, M.2
-
19
-
-
77949437221
-
Naturally occurring δ-hydroxy-γ-lactones: Muricatacins and related compounds
-
Murcia, M. C.; Navarro, C.; Moreno, A.; Csákÿ, A. G. Naturally occurring δ-hydroxy-γ-lactones: muricatacins and related compounds. Curr. Org. Chem. 2010, 14, 15-47
-
(2010)
Curr. Org. Chem
, vol.14
, pp. 15-47
-
-
Murcia, M.C.1
Navarro, C.2
Moreno, A.3
Csákÿ, A.G.4
-
20
-
-
29744469214
-
The application of olefin metathesis to the synthesis of biologically active macrocyclic agents
-
Van de Weghe, P.; Eustache, J. The application of olefin metathesis to the synthesis of biologically active macrocyclic agents. Curr. Top. Med. Chem. 2005, 5, 1495-1519.
-
(2005)
Curr. Top. Med. Chem
, vol.5
, pp. 1495-1519
-
-
van de Weghe, P.1
Eustache, J.2
-
21
-
-
2942589152
-
Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis
-
Deiters, A.; Martin, S. F. Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis. Chem. Rev. 2004, 104, 2199-2238
-
(2004)
Chem. Rev
, vol.104
, pp. 2199-2238
-
-
Deiters, A.1
Martin, S.F.2
-
22
-
-
33847623822
-
Stereoselective synthesis of naturally occurring 5,6-dihydropyran-2-ones
-
Marco, J. A.; Carda, M.; Murga, J.; Falomir, E. Stereoselective synthesis of naturally occurring 5,6-dihydropyran-2-ones. Tetrahedron 2007, 63, 2929-2958
-
(2007)
Tetrahedron
, vol.63
, pp. 2929-2958
-
-
Marco, J.A.1
Carda, M.2
Murga, J.3
Falomir, E.4
-
23
-
-
77953764647
-
Formation of fiveand six-membered heterocyclic compounds by ring closing metathesis
-
Majumdar, K. C.; Chattopadhyay, B.; Ray, K. Formation of fiveand six-membered heterocyclic compounds by ring closing metathesis. Curr. Org. Synth. 2010, 7, 153-176
-
(2010)
Curr. Org. Synth
, vol.7
, pp. 153-176
-
-
Majumdar, K.C.1
Chattopadhyay, B.2
Ray, K.3
-
24
-
-
78649664717
-
Recent applications of ring-closing metathesis in the synthesis of lactams and macrolactams
-
Hassan, H. M. A. Recent applications of ring-closing metathesis in the synthesis of lactams and macrolactams. Chem. Commun. 2010, 46, 9100-9106.
-
(2010)
Chem. Commun
, vol.46
, pp. 9100-9106
-
-
Hassan, H.M.A.1
-
25
-
-
0000680470
-
Application of olefin metathesis to organic synthesis. Synthesis of civetone and macrolides
-
Tsuji, J.; Hashiguchi, S. Application of olefin metathesis to organic synthesis. Synthesis of civetone and macrolides. Tetrahedron Lett. 1980, 21, 2955-2958.
-
(1980)
Tetrahedron Lett
, vol.21
, pp. 2955-2958
-
-
Tsuji, J.1
Hashiguchi, S.2
-
26
-
-
0001263185
-
The application of catalytic ring-closing olefin metathesis to the synthesis of unsaturated oxygen heterocycles
-
Fu, G. C.; Grubbs, R. H. The application of catalytic ring-closing olefin metathesis to the synthesis of unsaturated oxygen heterocycles. J. Am. Chem. Soc. 1992, 114, 5426-5427
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 5426-5427
-
-
Fu, G.C.1
Grubbs, R.H.2
-
27
-
-
0000587503
-
Synthesis of nitrogen heterocycles via catalytic ring-closing metathesis of dienes
-
Fu, G. C.; Grubbs, R. H. Synthesis of nitrogen heterocycles via catalytic ring-closing metathesis of dienes. J. Am. Chem. Soc. 1992, 114, 7324-7325
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 7324-7325
-
-
Fu, G.C.1
Grubbs, R.H.2
-
28
-
-
78249281266
-
Catalytic ring-closing metathesis of functionalized dienes by a ruthenium carbene complex
-
Fu, G. C.; Nguyen, S. T.; Grubbs, R. H. Catalytic ring-closing metathesis of functionalized dienes by a ruthenium carbene complex. J. Am. Chem. Soc. 1993, 115, 9856-9857.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 9856-9857
-
-
Fu, G.C.1
Nguyen, S.T.2
Grubbs, R.H.3
-
29
-
-
0000315733
-
Practical catalyst for cyclic metathesis. Synthesis of functional and/or enantiopure cycloalkenes
-
Nugent, W. A.; Feldman, J.; Calabrese, J. C. Practical catalyst for cyclic metathesis. Synthesis of functional and/or enantiopure cycloalkenes. J. Am. Chem. Soc. 1995, 117, 8992-8998.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 8992-8998
-
-
Nugent, W.A.1
Feldman, J.2
Calabrese, J.C.3
-
30
-
-
0001101871
-
Effect of olefin substitution on the ringclosing metathesis of dienes
-
Kirkland, T. A.; Grubbs, R. H. Effect of olefin substitution on the ringclosing metathesis of dienes. J. Org. Chem. 1997, 62, 7310-7318.
-
(1997)
J. Org. Chem
, vol.62
, pp. 7310-7318
-
-
Kirkland, T.A.1
Grubbs, R.H.2
-
31
-
-
0030051890
-
A formal synthesis of castanospermine using an olefin metathesis cyclisation reaction as a key step
-
Overkleeft, H. S.; Pandit, U. K. A formal synthesis of castanospermine using an olefin metathesis cyclisation reaction as a key step. Tetrahedron Lett. 1996, 37, 547-550.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 547-550
-
-
Overkleeft, H.S.1
Pandit, U.K.2
-
32
-
-
0038206375
-
Conformationally unbiased macrocyclization reactions by ring closing metathesis
-
Fürstner, A.; Langemann, K. Conformationally unbiased macrocyclization reactions by ring closing metathesis. J. Org. Chem. 1996, 61, 3942-3943.
-
(1996)
J. Org. Chem
, vol.61
, pp. 3942-3943
-
-
Fürstner, A.1
Langemann, K.2
-
33
-
-
0038163433
-
Total synthesis of (+)-ricinelaidic acid lactone and of (-)-gloeosporone based on transition-metal-catalyzed C-C bond formations
-
Fürstner, A.; Langemann, K. Total synthesis of (+)-ricinelaidic acid lactone and of (-)-gloeosporone based on transition-metal-catalyzed C-C bond formations. J. Am. Chem. Soc. 1997, 119, 9130-9136.
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 9130-9136
-
-
Fürstner, A.1
Langemann, K.2
-
34
-
-
0010515564
-
Unsaturated macrocyclic lactone synthesis via catalytic ring-closing metathesis
-
Litinas, K. E.; Salteris, B. E. Unsaturated macrocyclic lactone synthesis via catalytic ring-closing metathesis. J. Chem. Soc. Perkin Trans. 1 1997, 2869-2872.
-
(1997)
J. Chem. Soc. Perkin Trans. 1
, pp. 2869-2872
-
-
Litinas, K.E.1
Salteris, B.E.2
-
35
-
-
0002372178
-
Cationic ruthenium allenylidene complexes as a new class of performing catalysts for ring closing metathesis
-
Fürstner, A.; Picquet, M.; Bruneau, C.; Dixneuf, P. H. Cationic ruthenium allenylidene complexes as a new class of performing catalysts for ring closing metathesis. Chem. Commun. 1998, 1315-1316.
-
(1998)
Chem. Commun
, pp. 1315-1316
-
-
Fürstner, A.1
Picquet, M.2
Bruneau, C.3
Dixneuf, P.H.4
-
36
-
-
0037610332
-
A most user-friendly protocol for ring closing metathesis reactions
-
Fürstner, A.; Ackermann, L. A most user-friendly protocol for ring closing metathesis reactions. Chem. Commun. 1999, 95-96.
-
(1999)
Chem. Commun
, pp. 95-96
-
-
Fürstner, A.1
Ackermann, L.2
-
37
-
-
0035914638
-
Indenylidene complexes of ruthenium: Optimized synthesis, structure elucidation, and performance as catalysts for olefin metathesis - application to the synthesis of the ADE-ring system of nakadomarin A
-
Fürstner, A.; Guth, O.; Düffels, A.; Seidel, G.; Liebl, M.; Gabor, B.; Mynott, R. Indenylidene complexes of ruthenium: optimized synthesis, structure elucidation, and performance as catalysts for olefin metathesis - application to the synthesis of the ADE-ring system of nakadomarin A. Chem. Eur. J. 2001, 7, 4811-4820.
-
(2001)
Chem. Eur. J
, vol.7
, pp. 4811-4820
-
-
Fürstner, A.1
Guth, O.2
Düffels, A.3
Seidel, G.4
Liebl, M.5
Gabor, B.6
Mynott, R.7
-
38
-
-
0000021785
-
Reaction of neopentylidene complexes of the type M(CH-t-Bu)(N-2,6-C6H3-i-Pr2)(OR)2 (M = W, Mo) with methyl acrylate and N,N-dimethylacrylamide to give metallacyclobutane complexes
-
Feldman, J.; Murdzek, J. S.; Davis, W. M.; Schrock, R. R. Reaction of neopentylidene complexes of the type M(CH-t-Bu)(N-2,6-C6H3-i-Pr2)(OR)2 (M = W, Mo) with methyl acrylate and N,N-dimethylacrylamide to give metallacyclobutane complexes. Organometallics 1989, 8, 2260-2265.
-
(1989)
Organometallics
, vol.8
, pp. 2260-2265
-
-
Feldman, J.1
Murdzek, J.S.2
Davis, W.M.3
Schrock, R.R.4
-
39
-
-
0033804280
-
The role of ring strain on the ease of ring closure of bifunctional chain molecules
-
Galli, C.; Mandolini, L. The role of ring strain on the ease of ring closure of bifunctional chain molecules. Eur. J. Org. Chem. 2000, 3117-3125.
-
(2000)
Eur. J. Org. Chem
, pp. 3117-3125
-
-
Galli, C.1
Mandolini, L.2
-
40
-
-
0344972893
-
Stereocontrolled synthesis of the everninomicin A1B(A)C ring framework
-
Nicolaou, K. C.; Rodríguez, R. M.; Mitchell, H. J.; van Delft, F. L. Stereocontrolled synthesis of the everninomicin A1B(A)C ring framework. Angew. Chem. Int. Ed. 1998, 37, 1874-1876.
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 1874-1876
-
-
Nicolaou, K.C.1
Rodríguez, R.M.2
Mitchell, H.J.3
van Delft, F.L.4
-
41
-
-
0032566021
-
Ring-closing metathesis strategy to unsaturated γ-and δ-lactones: Synthesis of hydroxyethylene isostere for protease inhibitors
-
Ghosh, A. K.; Cappiello, J.; Shin, D. Ring-closing metathesis strategy to unsaturated γ-and δ-lactones: synthesis of hydroxyethylene isostere for protease inhibitors. Tetrahedron Lett. 1998, 39, 4651-4654.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4651-4654
-
-
Ghosh, A.K.1
Cappiello, J.2
Shin, D.3
-
42
-
-
0034728178
-
Asymmetric synthesis of goniothalamin, hexadecanolide, massoia lactone, and parascorbic acid via sequential allylboration-esterification ring-closing metathesis reactions
-
Ramachandran, P. V.; Reddy, M. V. R.; Brown, H. C. Asymmetric synthesis of goniothalamin, hexadecanolide, massoia lactone, and parascorbic acid via sequential allylboration-esterification ring-closing metathesis reactions. Tetrahedron Lett. 2000, 41, 583-586.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 583-586
-
-
Ramachandran, P.V.1
Reddy, M.V.R.2
Brown, H.C.3
-
43
-
-
0033551874
-
Double diastereoselection in asymmetric [2+3] cycloaddition of chiral oxazoline Noxides: Application to the kinetic resolution of a racemic a, b-unsaturated dlactone
-
Dirat, O.; Kouklovsky, C.; Langlois, Y.; Lesot, P.; Courtieu, J. Double diastereoselection in asymmetric [2+3] cycloaddition of chiral oxazoline Noxides: application to the kinetic resolution of a racemic a, b-unsaturated dlactone. Tetrahedron Asymmetry 1999, 10, 3197-3207.
-
(1999)
Tetrahedron Asymmetry
, vol.10
, pp. 3197-3207
-
-
Dirat, O.1
Kouklovsky, C.2
Langlois, Y.3
Lesot, P.4
Courtieu, J.5
-
44
-
-
0033533447
-
A Stereoselective synthesis of (-)-tetrahydrolipstatin
-
Ghosh, A. K.; Liu, C. A Stereoselective synthesis of (-)-tetrahydrolipstatin. Chem. Commun. 1999, 1743-1744.
-
(1999)
Chem. Commun
, pp. 1743-1744
-
-
Ghosh, A.K.1
Liu, C.2
-
45
-
-
0033612270
-
A short synthesis of the C1-C7 fragment of methymycin by ring-closing olefin metathesis
-
Cossy, J.; Bauer, D.; Bellosta, V. A short synthesis of the C1-C7 fragment of methymycin by ring-closing olefin metathesis. Tetrahedron Lett. 1999, 40, 4187-4188.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 4187-4188
-
-
Cossy, J.1
Bauer, D.2
Bellosta, V.3
-
46
-
-
0035959508
-
Regioselective ring-closing metathesis on terpenoid acrylates and acrylamides
-
Du, Y.; Wiemer, D. F. Regioselective ring-closing metathesis on terpenoid acrylates and acrylamides. Tetrahedron Lett. 2001, 42, 6069-6072.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 6069-6072
-
-
Du, Y.1
Wiemer, D.F.2
-
47
-
-
0037415524
-
Stereoselective synthesis of (-)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis
-
and references therein
-
Carda, M.; Rodríguez, S.; Castillo, E.; Bellido, A.; Díaz-Oltra, S.; Marco, J. A. Stereoselective synthesis of (-)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis. Tetrahedron 2003, 59, 857-864; and references therein.
-
(2003)
Tetrahedron
, vol.59
, pp. 857-864
-
-
Carda, M.1
Rodríguez, S.2
Castillo, E.3
Bellido, A.4
Díaz-Oltra, S.5
Marco, J.A.6
-
48
-
-
34547645846
-
Synthesis of alkylsubstituted six-membered lactones through ring-closing metathesis of homoallyl acrylates. An easy route to pyran-2-ones, constituents of tobacco flavor
-
D'Annibale, A.; Ciaralli, L.; Bassetti, M.; Pasquini, C. Synthesis of alkylsubstituted six-membered lactones through ring-closing metathesis of homoallyl acrylates. An easy route to pyran-2-ones, constituents of tobacco flavor. J. Org. Chem. 2007, 72, 6067-6074.
-
(2007)
J. Org. Chem
, vol.72
, pp. 6067-6074
-
-
D'Annibale, A.1
Ciaralli, L.2
Bassetti, M.3
Pasquini, C.4
-
49
-
-
0343777362
-
Total synthesis of everninomicin 13,384-1 - part 1: Retrosynthetic analysis and synthesis of the A1B(A)C fragment
-
Synthesis of pentenolides by RCM promoted by first-generation Grubbs catalysts
-
Synthesis of pentenolides by RCM promoted by first-generation Grubbs catalysts: (a) Nicolaou, K. C.; Rodríguez, R. M.; Mitchell, H. J.; Suzuki, H.; Fylaktakidou, K. C.; Baudoin, O.; van Delft, F. L. Total synthesis of everninomicin 13,384-1 - part 1: retrosynthetic analysis and synthesis of the A1B(A)C fragment. Chem. Eur. J. 2000, 6, 3095-3115
-
(2000)
Chem. Eur. J
, vol.6
, pp. 3095-3115
-
-
Nicolaou, K.C.1
Rodríguez, R.M.2
Mitchell, H.J.3
Suzuki, H.4
Fylaktakidou, K.C.5
Baudoin, O.6
van Delft, F.L.7
-
50
-
-
0035843312
-
Asymmetric synthesis of umuravumbolide
-
Reddy, M. V. R.; Rearick, J. P.; Hoch, N.; Ramachandran, P. V. Asymmetric synthesis of umuravumbolide. Org. Lett. 2001, 3, 19-20
-
(2001)
Org. Lett
, vol.3
, pp. 19-20
-
-
Reddy, M.V.R.1
Rearick, J.P.2
Hoch, N.3
Ramachandran, P.V.4
-
51
-
-
0035850265
-
Synthesis of the C1-C12 fragment of fostriecin
-
Cossy, J.; Pradaux, F.; BouzBouz, S. Synthesis of the C1-C12 fragment of fostriecin. Org. Lett. 2001, 3, 2233-2235
-
(2001)
Org. Lett
, vol.3
, pp. 2233-2235
-
-
Cossy, J.1
Pradaux, F.2
Bouzbouz, S.3
-
52
-
-
0035966208
-
Total synthesis of microtubule-stabilizing agent (-)-laulimalide
-
Ghosh, A. K.; Wang, Y.; Kim, J. T. Total synthesis of microtubule-stabilizing agent (-)-laulimalide. J. Org. Chem. 2001, 66, 8973-8982
-
(2001)
J. Org. Chem
, vol.66
, pp. 8973-8982
-
-
Ghosh, A.K.1
Wang, Y.2
Kim, J.T.3
-
53
-
-
0036329749
-
Stereoselective synthesis of the naturally occurring lactones (-)-osmundalactone and (-)-muricatacine using ring-closing metathesis
-
Carda, M.; Rodríguez, S.; González, F.; Castillo, E.; Villanueva, A.; Marco, J. A. Stereoselective synthesis of the naturally occurring lactones (-)-osmundalactone and (-)-muricatacine using ring-closing metathesis. Eur. J. Org. Chem. 2002, 2649-2655
-
(2002)
Eur. J. Org. Chem
, pp. 2649-2655
-
-
Carda, M.1
Rodríguez, S.2
González, F.3
Castillo, E.4
Villanueva, A.5
Marco, J.A.6
-
54
-
-
0037433834
-
An enantioselective synthesis of the C1-C9 segment of antitumor macrolide peloruside A
-
Ghosh, A. K.; Kim, J.-H. An enantioselective synthesis of the C1-C9 segment of antitumor macrolide peloruside A. Tetrahedron Lett. 2003, 44, 3967-3969
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 3967-3969
-
-
Ghosh, A.K.1
Kim, J.-H.2
-
55
-
-
0346157330
-
A practical enantioselective synthesis of massoialactone via hydrolytic kinetic resolution
-
Gupta, P.; Naidu, S. V.; Kumar, P. A practical enantioselective synthesis of massoialactone via hydrolytic kinetic resolution. Tetrahedron Lett. 2004, 45, 849-851.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 849-851
-
-
Gupta, P.1
Naidu, S.V.2
Kumar, P.3
-
56
-
-
0036418965
-
Synthesis of spirocyclic butenolides by ring closing metathesis
-
Langer, P.; Albrecht, U. Synthesis of spirocyclic butenolides by ring closing metathesis. Synlett 2002, 1841-1842
-
(2002)
Synlett
, pp. 1841-1842
-
-
Langer, P.1
Albrecht, U.2
-
57
-
-
33846346518
-
First asymmetric synthesis of both enantiomers of andirolactone
-
Li, Y.; Zhang, T.; Li, Y.-L. First asymmetric synthesis of both enantiomers of andirolactone. Tetrahedron Lett. 2007, 48, 1503-1505
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 1503-1505
-
-
Li, Y.1
Zhang, T.2
Li, Y.-L.3
-
58
-
-
34247271295
-
Synthesis of spirocyclic butenolides by ring closing metathesis
-
Albrecht, U.; Langer, P. Synthesis of spirocyclic butenolides by ring closing metathesis. Tetrahedron 2007, 63, 4648-4654.
-
(2007)
Tetrahedron
, vol.63
, pp. 4648-4654
-
-
Albrecht, U.1
Langer, P.2
-
59
-
-
18844454773
-
Synthesis of α,β- unsaturated 4,5-disubstituted γ-lactones via ring-closing metathesis catalyzed by the first-generation Grubbs' catalyst
-
Bassetti, M.; D'Annibale, A.; Fanfoni, A.; Minissi, F. Synthesis of α,β- unsaturated 4,5-disubstituted γ-lactones via ring-closing metathesis catalyzed by the first-generation Grubbs' catalyst. Org. Lett. 2005, 7, 1805-1808.
-
(2005)
Org. Lett
, vol.7
, pp. 1805-1808
-
-
Bassetti, M.1
D'Annibale, A.2
Fanfoni, A.3
Minissi, F.4
-
60
-
-
4143062538
-
Relay ring-closing metathesis (RRCM): A strategy for directing metal movement throughout olefin metathesis sequences
-
Hoye, T. R.; Jeffrey, C. S.; Tennakoon, M. A.; Wang, J.; Zhao, H. Relay ring-closing metathesis (RRCM): a strategy for directing metal movement throughout olefin metathesis sequences. J. Am. Chem. Soc. 2004, 126, 10210-10211.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 10210-10211
-
-
Hoye, T.R.1
Jeffrey, C.S.2
Tennakoon, M.A.3
Wang, J.4
Zhao, H.5
-
61
-
-
68949140962
-
Ruthenium-based olefin metathesis catalysts bearing N-heterocyclic carbene ligands
-
Samojowicz, C.; Bieniek, M.; Grela, K. Ruthenium-based olefin metathesis catalysts bearing N-heterocyclic carbene ligands. Chem. Rev. 2009, 109, 3708-3742.
-
(2009)
Chem. Rev
, vol.109
, pp. 3708-3742
-
-
Samojowicz, C.1
Bieniek, M.2
Grela, K.3
-
62
-
-
0034685462
-
Synthesis of functionalized olefins by cross and ring-closing metathesis
-
Chatterjee, A. K.; Morgan, J. P.; Scholl, M.; Grubbs, R. H. Synthesis of functionalized olefins by cross and ring-closing metathesis. J. Am. Chem. Soc. 2000, 122, 3783-3784
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 3783-3784
-
-
Chatterjee, A.K.1
Morgan, J.P.2
Scholl, M.3
Grubbs, R.H.4
-
63
-
-
0037620216
-
Ruthenium carbene complexes with N,Nbis(mesityl)imidazol-2-ylidene ligands: RCM catalysts of extended scope
-
Fürstner, A.; Thiel, O. R.; Ackermann, L.; Schanz, H.-J.; Nolan, S. P. Ruthenium carbene complexes with N,Nbis(mesityl)imidazol-2-ylidene ligands: RCM catalysts of extended scope. J. Org. Chem. 2000, 65, 2204-2207
-
(2000)
J. Org. Chem
, vol.65
, pp. 2204-2207
-
-
Fürstner, A.1
Thiel, O.R.2
Ackermann, L.3
Schanz, H.-J.4
Nolan, S.P.5
-
64
-
-
0034734340
-
Efficient and recyclable monomeric and dendritic Rubased metathesis catalysts
-
Garber, S. B.; Kingsbury, J. S.; Gray, B. L.; Hoveyda, A. H. Efficient and recyclable monomeric and dendritic Rubased metathesis catalysts. J. Am. Chem. Soc. 2000, 122, 8168-8179.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 8168-8179
-
-
Garber, S.B.1
Kingsbury, J.S.2
Gray, B.L.3
Hoveyda, A.H.4
-
65
-
-
0035977649
-
New insights into the mechanism of ruthenium-catalyzed olefin metathesis reactions
-
Sanford, M. S.; Ulman, M.; Grubbs, R. H. New insights into the mechanism of ruthenium-catalyzed olefin metathesis reactions. J. Am. Chem. Soc. 2001, 123, 749-750.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 749-750
-
-
Sanford, M.S.1
Ulman, M.2
Grubbs, R.H.3
-
66
-
-
0035944467
-
Olefin metathesis involving ruthenium enoic carbene complexes
-
Choi, T.-L.; Lee, C. W.; Chatterjee, A. K.; Grubbs, R. H. Olefin metathesis involving ruthenium enoic carbene complexes. J. Am. Chem. Soc. 2001, 123, 10417-10418.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 10417-10418
-
-
Choi, T.-L.1
Lee, C.W.2
Chatterjee, A.K.3
Grubbs, R.H.4
-
67
-
-
33748714103
-
Chemoenzymatic synthesis of optically active γ-alkyl-γ-butenolides
-
Fujii, M.; Fukumura, M.; Hori, Y.; Hirai, Y.; Akita, H.; Nakamura, K.; Toriizuka, K.; Ida, Y. Chemoenzymatic synthesis of optically active γ-alkyl-γ-butenolides. Tetrahedron: Asymmetry 2006, 17, 2292-2298.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2292-2298
-
-
Fujii, M.1
Fukumura, M.2
Hori, Y.3
Hirai, Y.4
Akita, H.5
Nakamura, K.6
Toriizuka, K.7
Ida, Y.8
-
68
-
-
0042693206
-
Catalytic enantioselective conjugate reduction of lactones and lactames
-
Hughes, G.; Kimura, M.; Buchwald, S. L. Catalytic enantioselective conjugate reduction of lactones and lactames. J. Am. Chem. Soc. 2003, 125, 11253-11258.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 11253-11258
-
-
Hughes, G.1
Kimura, M.2
Buchwald, S.L.3
-
69
-
-
0034632359
-
Concise synthesis of (S,S)-(+)-dehydrohomoancepsenolide
-
Fürstner, A.; Dierkes, T. Concise synthesis of (S,S)-(+)-dehydrohomoancepsenolide. Org. Lett. 2000, 2, 2463-2465.
-
(2000)
Org. Lett
, vol.2
, pp. 2463-2465
-
-
Fürstner, A.1
Dierkes, T.2
-
70
-
-
18144418558
-
A domino ring-closing metathesis as a key-step in the synthesis of chiral lactones from D-mannitol
-
Nay, B.; Gaboriaud-Kolar, N.; Bodo, B. A domino ring-closing metathesis as a key-step in the synthesis of chiral lactones from D-mannitol. Tetrahedron Lett. 2005, 46, 3867-3870.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 3867-3870
-
-
Nay, B.1
Gaboriaud-Kolar, N.2
Bodo, B.3
-
71
-
-
77955806531
-
Ring-closing metathesis of acrylates: A comparative study
-
Schmidt, B.; Geibler, D. Ring-closing metathesis of acrylates: a comparative study. ChemCatChem 2010, 2, 423-429.
-
(2010)
ChemCatChem
, vol.2
, pp. 423-429
-
-
Schmidt, B.1
Geibler, D.2
-
72
-
-
38949088658
-
Indenylidene-ruthenium complexes bearing saturated N-heterocyclic carbenes: Synthesis and catalytic investigation in olefn metathesis reactions
-
Monsaert, S.; Drozdzak, R.; Dragutan, V.; Dragutan, I.; Verpoort, F. Indenylidene-ruthenium complexes bearing saturated N-heterocyclic carbenes: synthesis and catalytic investigation in olefn metathesis reactions. Eur. J. Inorg. Chem. 2008, 432-440.
-
(2008)
Eur. J. Inorg. Chem
, pp. 432-440
-
-
Monsaert, S.1
Drozdzak, R.2
Dragutan, V.3
Dragutan, I.4
Verpoort, F.5
-
73
-
-
78751538864
-
The catalytic performance of Ru-NHC alkylidene complexes: PCy3 versus pyridine as the dissociating ligand
-
Krehl, S.; Geibler, D.; Hauke, S.; Kunz, O.; Staude, L.; Schmidt, B. The catalytic performance of Ru-NHC alkylidene complexes: PCy3 versus pyridine as the dissociating ligand. Beilstein J. Org. Chem. 2010, 6, 1188-1198.
-
(2010)
Beilstein J. Org. Chem
, vol.6
, pp. 1188-1198
-
-
Krehl, S.1
Geibler, D.2
Hauke, S.3
Kunz, O.4
Staude, L.5
Schmidt, B.6
-
74
-
-
3342982883
-
Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation
-
Michrowska, A.; Bujok, R.; Harutyunyan, S.; Sashuk, V.; Dolgonos, G.; Grela, K. Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: enhancement of catalyst activity through electronic activation. J. Am. Chem. Soc. 2004, 126, 9318-9325.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 9318-9325
-
-
Michrowska, A.1
Bujok, R.2
Harutyunyan, S.3
Sashuk, V.4
Dolgonos, G.5
Grela, K.6
-
75
-
-
0037355464
-
A good bargain: An inexpensive, air-stable ruthenium metathesis catalyst derived from α-asarone
-
Grela, K.; Kim, M. A good bargain: an inexpensive, air-stable ruthenium metathesis catalyst derived from α-asarone. Eur. J. Org. Chem. 2003, 963-966.
-
(2003)
Eur. J. Org. Chem
, pp. 963-966
-
-
Grela, K.1
Kim, M.2
-
76
-
-
0037049171
-
A PS-DES immobilized ruthenium carbene: A robust and easily recyclable catalyst for olefin metathesis
-
Grela, K.; Tryznowski, M.; Bieniek, M. A PS-DES immobilized ruthenium carbene: a robust and easily recyclable catalyst for olefin metathesis. Tetrahedron Lett. 2002, 43, 9055-9059.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 9055-9059
-
-
Grela, K.1
Tryznowski, M.2
Bieniek, M.3
-
77
-
-
79952161685
-
Catalytic enantioselective synthesis of naturally occurring butenolides via hetero-allylic alkylation and ring closing metathesis
-
Mao, B.; Geurts, K.; Fañanás-Mastral, M.; van Zijl, A. W.; Fletcher, S. P.; Minnaard, A. J.; Feringa, B. L. Catalytic enantioselective synthesis of naturally occurring butenolides via hetero-allylic alkylation and ring closing metathesis. Org. Lett. 2011, 13, 948-951.
-
(2011)
Org. Lett
, vol.13
, pp. 948-951
-
-
Mao, B.1
Geurts, K.2
Fañanás-Mastral, M.3
van Zijl, A.W.4
Fletcher, S.P.5
Minnaard, A.J.6
Feringa, B.L.7
-
78
-
-
33846925525
-
Synthesis of substituted butenolides by the ring closing metathesis of two electron deficient olefins: A general route to the natural products of paraconic acids class
-
Selvakumar, N.; Kumar, P. K.; Reddy, K. C. S.; Chary, B. C. Synthesis of substituted butenolides by the ring closing metathesis of two electron deficient olefins: a general route to the natural products of paraconic acids class. Tetrahedron Lett. 2007, 48, 2021-2024.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 2021-2024
-
-
Selvakumar, N.1
Kumar, P.K.2
Reddy, K.C.S.3
Chary, B.C.4
-
79
-
-
0035857579
-
Enantioselective synthesis of the ricciocarpins A and B
-
Held, C.; Fröhlich, R.; Metz, P. Enantioselective synthesis of the ricciocarpins A and B. Angew. Chem. Int. Ed. 2001, 40, 1058-1060.
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 1058-1060
-
-
Held, C.1
Fröhlich, R.2
Metz, P.3
-
80
-
-
0043011081
-
α-Phospono lactone analogues of cytidine and cytosine arabinoside diphosphates: Synthesis via ring closing metathesis
-
Chen, X.; Wiemer, D. F. α-Phospono lactone analogues of cytidine and cytosine arabinoside diphosphates: synthesis via ring closing metathesis. J. Org. Chem. 2003, 68, 6597-6604.
-
(2003)
J. Org. Chem
, vol.68
, pp. 6597-6604
-
-
Chen, X.1
Wiemer, D.F.2
-
81
-
-
0034639734
-
A stereoselective synthesis of (+)-boronolide
-
Ghosh, A. K.; Bilcer, G. A stereoselective synthesis of (+)-boronolide. Tetrahedron Lett. 2000, 41, 1003-1006
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 1003-1006
-
-
Ghosh, A.K.1
Bilcer, G.2
-
82
-
-
0037015434
-
Stereocontrolled synthesis of (+)-boronolide
-
Trost, B. M.; Yeh, V. S. C. Stereocontrolled synthesis of (+)-boronolide. Org. Lett. 2002, 4, 3513-3516
-
(2002)
Org. Lett
, vol.4
, pp. 3513-3516
-
-
Trost, B.M.1
Yeh, V.S.C.2
-
83
-
-
14644411770
-
Stereoselective synthesis of (+)-boronolide
-
Naidu, S. V.; Gupta, P.; Kumar, P. Stereoselective synthesis of (+)-boronolide. Tetrahedron Lett. 2005, 46, 2129-2131
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 2129-2131
-
-
Naidu, S.V.1
Gupta, P.2
Kumar, P.3
-
84
-
-
33748746243
-
A short stereoselective synthesis of (+)-boronolide
-
Raghavan, S.; Krishnaiah, V. A short stereoselective synthesis of (+)-boronolide. Tetrahedron Lett. 2006, 47, 7611-7614
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 7611-7614
-
-
Raghavan, S.1
Krishnaiah, V.2
-
85
-
-
29744452186
-
Stereoselective total synthesis of (+)-boronolide
-
Boruwa, J.; Barua, N. C. Stereoselective total synthesis of (+)-boronolide. Tetrahedron 2006, 62, 1193-1198
-
(2006)
Tetrahedron
, vol.62
, pp. 1193-1198
-
-
Boruwa, J.1
Barua, N.C.2
-
86
-
-
33646510101
-
Enantio-and diastereocontrolled total synthesis of (+)-boronolide
-
Kumar, P.; Naidu, S. V. Enantio-and diastereocontrolled total synthesis of (+)-boronolide. J. Org. Chem. 2006, 71, 3935-3941.
-
(2006)
J. Org. Chem
, vol.71
, pp. 3935-3941
-
-
Kumar, P.1
Naidu, S.V.2
-
87
-
-
0037191089
-
Enantioselective total synthesis of δ-lactonic marine natural products, (+)-tanikolide and (-)-malyngolide, via RCM reaction
-
Mizutani, H.; Watanabe, M.; Honda, T. Enantioselective total synthesis of δ-lactonic marine natural products, (+)-tanikolide and (-)-malyngolide, via RCM reaction. Tetrahedron 2002, 58, 8929-8936.
-
(2002)
Tetrahedron
, vol.58
, pp. 8929-8936
-
-
Mizutani, H.1
Watanabe, M.2
Honda, T.3
-
88
-
-
34248387352
-
Stereocontrolled total synthesis of (-)-kainic acid
-
Sakaguchi, H.; Tokuyama, H.; Fukuyama, T. Stereocontrolled total synthesis of (-)-kainic acid. Org. Lett. 2007, 9, 1635-1638.
-
(2007)
Org. Lett
, vol.9
, pp. 1635-1638
-
-
Sakaguchi, H.1
Tokuyama, H.2
Fukuyama, T.3
-
89
-
-
0348209611
-
A short olefin metathesis-based route to enantiomerically pure arylated dihydropyrans and α,β-unsaturated δ-valero lactones
-
Syntheses of pentenolides by RCM promoted by N-heterocyclic ruthenium carbene complexes
-
Syntheses of pentenolides by RCM promoted by N-heterocyclic ruthenium carbene complexes: (a) Wildemann, H.; Dünkelmann, P.; Müller, M.; Schmidt, B. A short olefin metathesis-based route to enantiomerically pure arylated dihydropyrans and α,β-unsaturated δ-valero lactones. J. Org. Chem. 2003, 68, 799-804
-
(2003)
J. Org. Chem
, vol.68
, pp. 799-804
-
-
Wildemann, H.1
Dünkelmann, P.2
Müller, M.3
Schmidt, B.4
-
90
-
-
50649084992
-
Prins and RCM protocols for the synthesis of the pheromones of the giant white butterfly Idea leuconoe
-
Sabitha, G.; Fatima, N.; Reddy, E. V.; Yadav, J. S. Prins and RCM protocols for the synthesis of the pheromones of the giant white butterfly Idea leuconoe. Tetrahedron Lett. 2008, 49, 6087-6089
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 6087-6089
-
-
Sabitha, G.1
Fatima, N.2
Reddy, E.V.3
Yadav, J.S.4
-
91
-
-
69849114338
-
A concise total synthesis of saliniketal B
-
Liu, J.; De Brabander, J. K. A concise total synthesis of saliniketal B. J. Am. Chem. Soc. 2009, 131, 12562-12563.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 12562-12563
-
-
Liu, J.1
de Brabander, J.K.2
-
92
-
-
84858187788
-
β-Unsaturated δ-valerolactones through RCMisomerization sequence
-
Schmidt, B.; Kunz, O. α,β-Unsaturated δ-valerolactones through RCMisomerization sequence. Synlett 2012, 23, 851-854.
-
(2012)
Synlett
, vol.23
, pp. 851-854
-
-
Schmidt, B.1
Kunz, O.2
-
93
-
-
34250325511
-
Alkene metathesis: The search for better catalysts
-
Deshmukh, P. H.; Blechert, S. Alkene metathesis: the search for better catalysts. Dalton Trans. 2007, 2479-2491.
-
(2007)
Dalton Trans
, pp. 2479-2491
-
-
Deshmukh, P.H.1
Blechert, S.2
-
94
-
-
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.
-
(2010)
Chem. Rev
, vol.110
, pp. 1746-1787
-
-
Vougioukalakis, G.C.1
Grubbs, R.H.2
-
95
-
-
34147174302
-
Ruthenium-catalyzed ring-closing metathesis to form tetrasubstituted olefins
-
Berlin, J. M.; Campbell, K.; Ritter, T.; Funk, T. W.; Chlenov, A.; Grubbs, R. H. Ruthenium-catalyzed ring-closing metathesis to form tetrasubstituted olefins. Org. Lett. 2007, 9, 1339-1342
-
(2007)
Org. Lett
, vol.9
, pp. 1339-1342
-
-
Berlin, J.M.1
Campbell, K.2
Ritter, T.3
Funk, T.W.4
Chlenov, A.5
Grubbs, R.H.6
-
96
-
-
34247487884
-
Highly efficient ruthenium catalysts for the formation of tetrasubstituted olefins via ring-closing metathesis
-
Stewart, I. C.; Ung, T.; Pletnev, A. A.; Berlin, J. M.; Grubbs, R. H.; Schrodi, Y. Highly efficient ruthenium catalysts for the formation of tetrasubstituted olefins via ring-closing metathesis. Org. Lett. 2007, 9, 1589-1592
-
(2007)
Org. Lett
, vol.9
, pp. 1589-1592
-
-
Stewart, I.C.1
Ung, T.2
Pletnev, A.A.3
Berlin, J.M.4
Grubbs, R.H.5
Schrodi, Y.6
-
97
-
-
50049092322
-
A hexafluorobenzene promoted ring-closing metathesis to form tetrasubstituted olefins
-
Rost, D.; Porta, M.; Gessler, S.; Blechert, S. A hexafluorobenzene promoted ring-closing metathesis to form tetrasubstituted olefins. Tetrahedron Lett. 2008, 49, 5968-5971
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 5968-5971
-
-
Rost, D.1
Porta, M.2
Gessler, S.3
Blechert, S.4
-
98
-
-
70349921088
-
An [(NHC)(NHCEWG)RuCl2(CHPh)] complex for the efficient formation of sterically hindered olefins by ring-closing metathesis
-
Vorfalt, T.; Leuthäuber, S.; Plenio, H. An [(NHC)(NHCEWG)RuCl2(CHPh)] complex for the efficient formation of sterically hindered olefins by ring-closing metathesis. Angew. Chem. Int. Ed. 2009, 48, 5191-5194.
-
(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 5191-5194
-
-
Vorfalt, T.1
Leuthäuber, S.2
Plenio, H.3
-
99
-
-
80051995817
-
Microwave-assisted ruthenium-catalyzed olefin metathesis in fluorinated aromatic hydrocarbons: A beneficial combination
-
Samojowicz, C.; Borré, E.; Mauduit, M.; Grela, K. Microwave-assisted ruthenium-catalyzed olefin metathesis in fluorinated aromatic hydrocarbons: a beneficial combination. Adv. Synth. Cat. 2011, 353, 1993-2002.
-
(2011)
Adv. Synth. Cat
, vol.353
, pp. 1993-2002
-
-
Samojowicz, C.1
Borré, E.2
Mauduit, M.3
Grela, K.4
-
100
-
-
14544270505
-
Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis
-
Matsugi, M.; Curran, D. P. Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis. J. Org. Chem. 2005, 70, 1636-1642.
-
(2005)
J. Org. Chem
, vol.70
, pp. 1636-1642
-
-
Matsugi, M.1
Curran, D.P.2
-
101
-
-
84863661501
-
Removing ruthenium residues from olefin metathesis reaction products
-
Vougioukalakis, G. C. Removing ruthenium residues from olefin metathesis reaction products. Chem. Eur. J. 2012, 18, 8868-8880.
-
(2012)
Chem. Eur. J
, vol.18
, pp. 8868-8880
-
-
Vougioukalakis, G.C.1
-
102
-
-
0030137058
-
Acetogenins from Annonaceae, inhibitors of mitochondrial complex I
-
Zafra-Polo, M. C.; González, M. C., Estornell, E.; Sahpaz, S.; Cortes, D. Acetogenins from Annonaceae, inhibitors of mitochondrial complex I. Phytochemistry, 1996, 42, 253-271
-
(1996)
Phytochemistry
, vol.42
, pp. 253-271
-
-
Zafra-Polo, M.C.1
González, M.C.2
Estornell, E.3
Sahpaz, S.4
Cortes, D.5
-
103
-
-
0032145138
-
Natural acetogenins from Annonaceae, synthesis and mechanisms of action
-
Zafra-Polo, M. C.; Figadère, B.; Gallardo, T.; Tormo, J. R.; Cortes, D. Natural acetogenins from Annonaceae, synthesis and mechanisms of action. Phytochemistry, 1998, 48, 1087-1117
-
(1998)
Phytochemistry
, vol.48
, pp. 1087-1117
-
-
Zafra-Polo, M.C.1
Figadère, B.2
Gallardo, T.3
Tormo, J.R.4
Cortes, D.5
-
104
-
-
17844386379
-
Acetogenins from Annonaceae: Recent progress in isolation, synthesis and mechanisms of action
-
Bermejo, A.; Figadère, B.; Zafra-Polo, M. C.; Barrachina, I.; Estornell, E.; Cortes, D. Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action. Nat. Prod. Rep. 2005, 22, 269-303.
-
(2005)
Nat. Prod. Rep
, vol.22
, pp. 269-303
-
-
Bermejo, A.1
Figadère, B.2
Zafra-Polo, M.C.3
Barrachina, I.4
Estornell, E.5
Cortes, D.6
-
105
-
-
5644229532
-
Enantioselective total synthesis of (+)-gigantecin: Exploiting the asymmetric glycolate aldol reaction
-
M. T. Crimmins,; She, J. Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction. J. Am. Chem. Soc. 2004, 126, 12790-12791.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 12790-12791
-
-
Crimmins, M.T.1
She, J.2
-
106
-
-
17444416491
-
Asymmetric total synthesis of rollicosin
-
Quinn, K. J.; Isaacs, A. K.; DeChristopher, B. A.; Szklarz, S. C.; Arvary, R. A. Asymmetric total synthesis of rollicosin. Org. Lett. 2005, 7, 1243-1245.
-
(2005)
Org. Lett
, vol.7
, pp. 1243-1245
-
-
Quinn, K.J.1
Isaacs, A.K.2
Dechristopher, B.A.3
Szklarz, S.C.4
Arvary, R.A.5
-
107
-
-
34247648638
-
Convergent total synthesis of squamostolide
-
Quinn, K. J.; Smith, G. A.; Cammarano, C. M. Convergent total synthesis of squamostolide. Tetrahedron 2007, 63, 4881-4886.
-
(2007)
Tetrahedron
, vol.63
, pp. 4881-4886
-
-
Quinn, K.J.1
Smith, G.A.2
Cammarano, C.M.3
-
108
-
-
9444286984
-
Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis
-
Quinn, K. J.; Isaacs, A. K.; Arvary, R. A. Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis. Org. Lett. 2004, 6, 4143-4145
-
(2004)
Org. Lett
, vol.6
, pp. 4143-4145
-
-
Quinn, K.J.1
Isaacs, A.K.2
Arvary, R.A.3
-
109
-
-
57149090059
-
Facile enantiospecific synthesis of (-)-muricatacin
-
for other metathetic syntheses see, and Ref. 29e
-
for other metathetic syntheses see: Prasad, K. R.; Gandi, V. Facile enantiospecific synthesis of (-)-muricatacin. Tetrahedron: Asymmetry 2008, 19, 2616-2619, and Ref. 29e.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 2616-2619
-
-
Prasad, K.R.1
Gandi, V.2
-
110
-
-
5644268087
-
Domino ring-closing metathesis/intramolecular transfer of an alkenyl subunit: A direct formation of functionalized butenolides and pyrones from α,β- and β,γ-unsaturated esters
-
Virolleaud, M.-A.; Piva, O. Domino ring-closing metathesis/intramolecular transfer of an alkenyl subunit: a direct formation of functionalized butenolides and pyrones from α,β- and β,γ-unsaturated esters. Synlett 2004, 2087-2090.
-
(2004)
Synlett
, pp. 2087-2090
-
-
Virolleaud, M.-A.1
Piva, O.2
-
111
-
-
28844501313
-
Total synthesis of (+)-phomopsolide C by ringsize selective ring-closing metathesis/cross-metathesis
-
Michaelis, S.; Blechert, S. Total synthesis of (+)-phomopsolide C by ringsize selective ring-closing metathesis/cross-metathesis. Org. Lett. 2005, 7, 5513-5516.
-
(2005)
Org. Lett
, vol.7
, pp. 5513-5516
-
-
Michaelis, S.1
Blechert, S.2
-
112
-
-
67049174164
-
Asymmetric total synthesis of pyranicin
-
Crimmins, M. T.; Jacobs, D. L. Asymmetric total synthesis of pyranicin. Org. Lett. 2009, 11, 2695-2698.
-
(2009)
Org. Lett
, vol.11
, pp. 2695-2698
-
-
Crimmins, M.T.1
Jacobs, D.L.2
-
113
-
-
34548406439
-
A new chemoenzymatic Baylis- Hillman approach for the synthesis of enantiomerically enriched umbelactones
-
Kamal, A.; Krishnaji, T.; Reddy P. V. A new chemoenzymatic Baylis- Hillman approach for the synthesis of enantiomerically enriched umbelactones. Tetrahedron Lett. 2007, 48, 7232-7235.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 7232-7235
-
-
Kamal, A.1
Krishnaji, T.2
Reddy, P.V.3
-
114
-
-
84863643132
-
Stereoselective total synthesis of botryolide E
-
Veeranjaneyulu, B; Srilatha, M.; Reddy, G. C.; Das, B. Stereoselective total synthesis of botryolide E. Helv. Chim. Acta 2012, 95, 1152-1157.
-
(2012)
Helv. Chim. Acta
, vol.95
, pp. 1152-1157
-
-
Veeranjaneyulu, B.1
Srilatha, M.2
Reddy, G.C.3
Das, B.4
-
115
-
-
33645459127
-
Palladium-catalyzed asymmetric allylic alkylation of meso-and dl-1,2-divinylethylene carbonate
-
Trost, B. M.; Aponick, A. Palladium-catalyzed asymmetric allylic alkylation of meso-and dl-1,2-divinylethylene carbonate. J. Am. Chem. Soc. 2006, 128, 3931-3933
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 3931-3933
-
-
Trost, B.M.1
Aponick, A.2
-
116
-
-
79955466292
-
Enantioselective total synthesis of iso-cladospolide B, cladospolide C and cladospolide B from tartaric acid
-
Prasad K. R.; Gandi, V. R. Enantioselective total synthesis of iso-cladospolide B, cladospolide C and cladospolide B from tartaric acid. Tetrahedron: Asymmetry 2011, 22, 499-505.
-
(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 499-505
-
-
Prasad, K.R.1
Gandi, V.R.2
-
117
-
-
34848845804
-
Synthesis of butenolides recently isolated from marine microorganisms
-
Karlsson, S.; Andersson, F.; Breistein, P.; Hedenström, E. Synthesis of butenolides recently isolated from marine microorganisms. Tetrahedron Lett. 2007, 48, 7878-7881
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 7878-7881
-
-
Karlsson, S.1
Andersson, F.2
Breistein, P.3
Hedenström, E.4
-
118
-
-
48949114920
-
Total synthesis of (4S,10R)-4-hydroxy-10-methyl-11-oxododec-2-en-1,4-olide and related bioactive marine butenolides
-
Dai, W.-M.; Shi, L.; Li, Y. Total synthesis of (4S,10R)-4-hydroxy-10-methyl-11-oxododec-2-en-1,4-olide and related bioactive marine butenolides. Tetrahedron: Asymmetry 2008, 19, 1549-1556
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 1549-1556
-
-
Dai, W.-M.1
Shi, L.2
Li, Y.3
-
119
-
-
70549114932
-
Total synthesis of diastereomeric marine butenolides possessing a syn-aldol subunit at C10 and C11 and the related C11-ketone
-
Wang, Y.; Dai, W.-M. Total synthesis of diastereomeric marine butenolides possessing a syn-aldol subunit at C10 and C11 and the related C11-ketone. Tetrahedron 2010, 66, 187-196.
-
(2010)
Tetrahedron
, vol.66
, pp. 187-196
-
-
Wang, Y.1
Dai, W.-M.2
-
120
-
-
0037194197
-
Elaboration of a Baylis- Hillman adduct to (-)-acaterin and its diastereomer through ring closing metathesis
-
Anand, R. V.; Baktharaman, S.; Singh, V. K. Elaboration of a Baylis- Hillman adduct to (-)-acaterin and its diastereomer through ring closing metathesis. Tetrahedron Lett. 2002, 43, 5393-5395.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5393-5395
-
-
Anand, R.V.1
Baktharaman, S.2
Singh, V.K.3
-
121
-
-
2442666296
-
Use of a Baylis-Hillman adduct in the stereoselective synthesis of syributins via a RCM protocol
-
Krishna, P. R.; Narsingam, M.; Kannan, V. Use of a Baylis-Hillman adduct in the stereoselective synthesis of syributins via a RCM protocol. Tetrahedron Lett. 2004, 45, 4773-4775
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 4773-4775
-
-
Krishna, P.R.1
Narsingam, M.2
Kannan, V.3
-
122
-
-
77956185673
-
Chiron approach for the formal synthesis of (+)-syributin 1
-
Gautam, D.; Rao, B. V. Chiron approach for the formal synthesis of (+)-syributin 1. Tetrahedron: Asymmetry 2010, 21, 2087-2091.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2087-2091
-
-
Gautam, D.1
Rao, B.V.2
-
123
-
-
79956119071
-
Total synthesis of (-)-Sessilifoliamide C and (-)-8-epi-Stemoamide
-
Hoye, A. T.; Wipf, P. Total synthesis of (-)-Sessilifoliamide C and (-)-8-epi-Stemoamide. Org. Lett. 2011, 13, 2634-2637.
-
(2011)
Org. Lett
, vol.13
, pp. 2634-2637
-
-
Hoye, A.T.1
Wipf, P.2
-
124
-
-
77950342103
-
Isolation and total syntheses of two new alkaloids, dubiusamines-A, and -B, from
-
Tan, M. A.; Kitajima, M.; Kogure, N.; Nonato, M. G.; Takayama, H. Isolation and total syntheses of two new alkaloids, dubiusamines-A, and -B, from Pandanus dubius. Tetrahedron 2010, 66, 3353-3359.
-
(2010)
Pandanus Dubius. Tetrahedron
, vol.66
, pp. 3353-3359
-
-
Tan, M.A.1
Kitajima, M.2
Kogure, N.3
Nonato, M.G.4
Takayama, H.5
-
125
-
-
0031047562
-
Cytotoxicity and electron microscopy of cell death induced by goniothalamin
-
Ali, A. M.; Mckeen, M. M.; Hamid, M.; Aun, Q. B.; Zauyah, Y.; Azimahtol, H. L. P.; Kawazu, K. Cytotoxicity and electron microscopy of cell death induced by goniothalamin. Planta Medica 1997, 63, 81-83
-
(1997)
Planta Medica
, vol.63
, pp. 81-83
-
-
Ali, A.M.1
McKeen, M.M.2
Hamid, M.3
Aun, Q.B.4
Zauyah, Y.5
Azimahtol, H.L.P.6
Kawazu, K.7
-
126
-
-
0344172153
-
Semisynthesis and citotoxicity of styryl-lactone derivatives
-
Bermejo, A.; Léonce, S.; Cabedo, N.; Andreu, I.; Caignard, D. H.; Atassi, G.; Cortes, D. Semisynthesis and citotoxicity of styryl-lactone derivatives. J. Nat. Prod. 1999, 62, 1106-1109
-
(1999)
J. Nat. Prod
, vol.62
, pp. 1106-1109
-
-
Bermejo, A.1
Léonce, S.2
Cabedo, N.3
Andreu, I.4
Caignard, D.H.5
Atassi, G.6
Cortes, D.7
-
127
-
-
0038674623
-
Citotoxic styrylpyrones from
-
Lan, Y.-H.; Chang, F.-R.; Yu, J.-H.; Yang, Y.-L.; Chang, Y.-L.; Lee, S.-J.; Wu, Y.-C. Citotoxic styrylpyrones from Goniothalamus amuyon. J. Nat. Prod. 2003, 66, 487-490.
-
(2003)
Goniothalamus Amuyon. J. Nat. Prod
, vol.66
, pp. 487-490
-
-
Lan, Y.-H.1
Chang, F.-R.2
Yu, J.-H.3
Yang, Y.-L.4
Chang, Y.-L.5
Lee, S.-J.6
Wu, Y.-C.7
-
128
-
-
0346334600
-
Synthesis of (+)-goniothalamin and its enantiomer by combination of lipase catalyzed resolution and alkene metathesis
-
Sundby, E.; Perk, L.; Anthonsen, T.; Aasen, A. J.; Hansen, T. V. Synthesis of (+)-goniothalamin and its enantiomer by combination of lipase catalyzed resolution and alkene metathesis. Tetrahedron 2004, 60, 521-524
-
(2004)
Tetrahedron
, vol.60
, pp. 521-524
-
-
Sundby, E.1
Perk, L.2
Anthonsen, T.3
Aasen, A.J.4
Hansen, T.V.5
-
129
-
-
0742304466
-
Short and efficient chemoenzymatic synthesis of goniothalamin
-
Gruttadauria, M.; Lo Meo, P.; Noto, R. Short and efficient chemoenzymatic synthesis of goniothalamin. Tetrahedron Lett. 2004, 45, 83-85.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 83-85
-
-
Gruttadauria, M.1
Lo, M.P.2
Noto, R.3
-
130
-
-
15344340419
-
(R)-Goniothalamin: Total syntheses and cytotoxic activity against cancer cell lines
-
de Fatima, A.; Kohn, L. K.; Antonio, M. A.; de Carvalho, J. E.; Pilli R. A. (R)-Goniothalamin: total syntheses and cytotoxic activity against cancer cell lines. Bioorg. Med. Chem. 2005, 13, 2927-2933
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 2927-2933
-
-
de Fatima, A.1
Kohn, L.K.2
Antonio, M.A.3
de Carvalho, J.E.4
Pilli, R.A.5
-
131
-
-
33745738416
-
Total synthesis of (R)-(+)-goniothalamin and (R)-(+)-goniothalamin oxide: First application in the sulfoxide-modified Julia olefination in total synthesis
-
Pospíil, J.; Markó, I. E. Total synthesis of (R)-(+)-goniothalamin and (R)-(+)-goniothalamin oxide: first application in the sulfoxide-modified Julia olefination in total synthesis. Tetrahedron Lett. 2006, 47, 5933-5937
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 5933-5937
-
-
Pospíil, J.1
Markó, I.E.2
-
132
-
-
65749119407
-
De novo asymmetric synthesis of (+)-goniothalamin, (+)-goniothalamin oxide and 7,8-bis-epi-goniothalamin using asymmetric allylations
-
Harsh, P.; O'Doherty, G. A. De novo asymmetric synthesis of (+)-goniothalamin, (+)-goniothalamin oxide and 7,8-bis-epi-goniothalamin using asymmetric allylations. Tetrahedron 2009, 65, 5051-5055.
-
(2009)
Tetrahedron
, vol.65
, pp. 5051-5055
-
-
Harsh, P.1
O'Doherty, G.A.2
-
133
-
-
38649100324
-
Metathesis-based synthesis of 3-methoxy α,β unsaturated lactones: Total synthesis of (R)-Kavain and of C1-C6 fragment of jerangolide D
-
Pospíil, J.; Markó, I.E. Metathesis-based synthesis of 3-methoxy α,β unsaturated lactones: total synthesis of (R)-Kavain and of C1-C6 fragment of jerangolide D. Tetrahedron Lett. 2008, 49, 1523-1526.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 1523-1526
-
-
Pospíil, J.1
Markó, I.E.2
-
134
-
-
0142023994
-
Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts
-
Schrock, R. R.; Hoveyda, A. H. Molybdenum and tungsten imido alkylidene complexes as efficient olefin-metathesis catalysts. Angew. Chem. Int. Ed. 2003, 42, 4592-4633.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4592-4633
-
-
Schrock, R.R.1
Hoveyda, A.H.2
-
135
-
-
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
-
(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
-
136
-
-
15444379755
-
Synthetic approaches and total synthesis of natural zoapatanol
-
Taillier, C.; Gille, B.; Bellosta, V.; Cossy, J. Synthetic approaches and total synthesis of natural zoapatanol. J. Org. Chem. 2005, 70, 2097-2108
-
(2005)
J. Org. Chem
, vol.70
, pp. 2097-2108
-
-
Taillier, C.1
Gille, B.2
Bellosta, V.3
Cossy, J.4
-
137
-
-
32944480843
-
Total synthesis of gambierol: The generation of the A-C and F-H subunits by using a Cglycoside centered strategy
-
Majumder, U.; Cox, J. M.; Johnson, H. W. B.; Rainier, J. D. Total synthesis of gambierol: the generation of the A-C and F-H subunits by using a Cglycoside centered strategy. Chem. Eur. J. 2006, 12, 1736-1746.
-
(2006)
Chem. Eur. J
, vol.12
, pp. 1736-1746
-
-
Majumder, U.1
Cox, J.M.2
Johnson, H.W.B.3
Rainier, J.D.4
-
138
-
-
79953267024
-
Stereoselective total synthesis of cryptopyranmoscatone A1
-
Sabitha, G.; Reddy, S. S. S.; Yadav, J. S. Stereoselective total synthesis of cryptopyranmoscatone A1. Tetrahedron Lett. 2011, 52, 2407-2409.
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 2407-2409
-
-
Sabitha, G.1
Reddy, S.S.S.2
Yadav, J.S.3
-
139
-
-
84858708256
-
The first stereoselective total synthesis of (Z)-cryptomoscatone D2, a natural G2 checkpoint inhibitor
-
Reddy, G. C.; Balasubramanyam, P.; Salvanna, N.; Reddy, T. S.; Das, B. The first stereoselective total synthesis of (Z)-cryptomoscatone D2, a natural G2 checkpoint inhibitor. Bioorg. Med. Chem. Lett. 2012, 22, 2415-2417.
-
(2012)
Bioorg. Med. Chem. Lett
, vol.22
, pp. 2415-2417
-
-
Reddy, G.C.1
Balasubramanyam, P.2
Salvanna, N.3
Reddy, T.S.4
Das, B.5
-
140
-
-
79251598600
-
Total synthesis of (-)-diospongin A and (+)- cryptofolione via asymmetric aldol reaction
-
Kumar, R. N.; Meshram, H. M. Total synthesis of (-)-diospongin A and (+)- cryptofolione via asymmetric aldol reaction. Tetrahedron Lett. 2011, 52, 1003-1007.
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 1003-1007
-
-
Kumar, R.N.1
Meshram, H.M.2
-
141
-
-
79955982082
-
The first total synthesis of (-)- bitungolide E
-
Shashidhar, J.; Reddy, K. M.; Ghosh, S. The first total synthesis of (-)- bitungolide E. Tetrahedron Lett. 2011, 52, 3106-3109.
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 3106-3109
-
-
Shashidhar, J.1
Reddy, K.M.2
Ghosh, S.3
-
142
-
-
39349090260
-
Total Synthesis of (-)-bitungolide F and determination of its absolute stereochemistry
-
Ghosh, S.; Kumar, S. U.; Shashidhar, J. Total Synthesis of (-)-bitungolide F and determination of its absolute stereochemistry. J. Org. Chem. 2008, 73, 1582-1585
-
(2008)
J. Org. Chem
, vol.73
, pp. 1582-1585
-
-
Ghosh, S.1
Kumar, S.U.2
Shashidhar, J.3
-
143
-
-
77956601843
-
Two concise totally syntheses of (-)-bitungolide F
-
ElMarrouni, A.; Joolakanti, S. R.; Colon, A.; Heras, M.; Arseniyadis, S.; Cossy, J. Two concise totally syntheses of (-)-bitungolide F. Org. Lett. 2010, 12, 4074-4077.
-
(2010)
Org. Lett
, vol.12
, pp. 4074-4077
-
-
Elmarrouni, A.1
Joolakanti, S.R.2
Colon, A.3
Heras, M.4
Arseniyadis, S.5
Cossy, J.6
-
144
-
-
71049142266
-
Stereoselective total synthesis of a potent natural antifungal compound (6S)-5,6,dihydro-6-[(2R)-2-hydroxy-6-phenyl hexyl]-2H-pyran-2-one
-
Das, B.; Laxminarayana, K.; Krishnaiah, M.; Kumar, D. N. Stereoselective total synthesis of a potent natural antifungal compound (6S)-5,6,dihydro-6-[(2R)-2-hydroxy-6-phenyl hexyl]-2H-pyran-2-one. Bioorg. Med. Chem. Lett. 2009, 19, 6396-6398
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 6396-6398
-
-
Das, B.1
Laxminarayana, K.2
Krishnaiah, M.3
Kumar, D.N.4
-
145
-
-
61549112213
-
Stereoselective synthesis of (6S) and (6R)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one and their cytotoxic activity against cancer cell lines
-
Narasimhulu, M.; Krishna, A. S.; Rao, J. V.; Venkateswarlu, Y. Stereoselective synthesis of (6S) and (6R)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one and their cytotoxic activity against cancer cell lines. Tetrahedron 2009, 65, 2989-2994
-
(2009)
Tetrahedron
, vol.65
, pp. 2989-2994
-
-
Narasimhulu, M.1
Krishna, A.S.2
Rao, J.V.3
Venkateswarlu, Y.4
-
146
-
-
82255192248
-
An organocatalytic route to the synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one and ravensara lactones
-
Dwivedi, N.; Tripathi, D.; Kumar, P. An organocatalytic route to the synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one and ravensara lactones. Tetrahedron: Asymmetry 2011, 22, 1749-1756.
-
(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 1749-1756
-
-
Dwivedi, N.1
Tripathi, D.2
Kumar, P.3
-
147
-
-
77956390206
-
Regioselective tandem ring closing/cross metathesis of 1,5-hexadien-3-ol derivatives: Application to the total synthesis of rugulactone
-
Cros, F.; Pelotier, B.; Piva, O. Regioselective tandem ring closing/cross metathesis of 1,5-hexadien-3-ol derivatives: application to the total synthesis of rugulactone. Eur. J. Org. Chem. 2010, 5063-5070
-
(2010)
Eur. J. Org. Chem
, pp. 5063-5070
-
-
Cros, F.1
Pelotier, B.2
Piva, O.3
-
148
-
-
79960566932
-
Stereoselective total synthesis of rugulactone
-
Das, B.; Srinivas, Y.; Sudhakar, C.; Reddy, P. R. Stereoselective total synthesis of rugulactone. Helv. Chim. Acta 2011, 94, 1290-1295.
-
(2011)
Helv. Chim. Acta
, vol.94
, pp. 1290-1295
-
-
Das, B.1
Srinivas, Y.2
Sudhakar, C.3
Reddy, P.R.4
-
149
-
-
0037131291
-
Stereoselective Syntheses of (+)-goniodiol, (-)-8-epigoniodiol, and (+)-9-deoxygoniopypyrone via alkoxyallylboration and ring-closing metathesis
-
Ramachandran, P. V.; Chandra, J. S.; Reddy, M. V. R. Stereoselective Syntheses of (+)-goniodiol, (-)-8-epigoniodiol, and (+)-9-deoxygoniopypyrone via alkoxyallylboration and ring-closing metathesis. J. Org. Chem. 2002, 67, 7547-7550
-
(2002)
J. Org. Chem
, vol.67
, pp. 7547-7550
-
-
Ramachandran, P.V.1
Chandra, J.S.2
Reddy, M.V.R.3
-
150
-
-
78650253408
-
A concise enantioselective synthesis of (+)-goniodiol and (+)-8-methoxygoniodiol via Co-catalyzed HKR of anti-(2SR,3RS)-3-methoxy-3-phenyl-1,2-epoxypropane
-
Kiran, I. N. C.; Reddy, R. S.; Suryavanshi, G.; Sudalai, A. A concise enantioselective synthesis of (+)-goniodiol and (+)-8-methoxygoniodiol via Co-catalyzed HKR of anti-(2SR,3RS)-3-methoxy-3-phenyl-1,2-epoxypropane. Tetrahedron Lett. 2011, 52, 438-440
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 438-440
-
-
Kiran, I.N.C.1
Reddy, R.S.2
Suryavanshi, G.3
Sudalai, A.4
-
151
-
-
80054093901
-
A Morita-Baylis-Hillman adduct allows the diastereoselective synthesis of styryl lactones
-
Paioti, P. H. S.; Coelho, F. A Morita-Baylis-Hillman adduct allows the diastereoselective synthesis of styryl lactones. Tetrahedron Lett. 2011, 52, 6180-6184.
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 6180-6184
-
-
Paioti, P.H.S.1
Coelho, F.2
-
152
-
-
53849105118
-
Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine
-
Álvarez-Bercedo, P.; Falomir, E.; Murga, J.; Carda, M.; Marco, J. A. Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine. Eur. J. Org. Chem. 2008, 4015-4018
-
(2008)
Eur. J. Org. Chem
, pp. 4015-4018
-
-
Álvarez-Bercedo, P.1
Falomir, E.2
Murga, J.3
Carda, M.4
Marco, J.A.5
-
153
-
-
67651099034
-
Stereoselective total synthesis of dodoneine
-
Das, B.; Suneel, K.; Satyalakshmi, G.; Kumar, D. N. Stereoselective total synthesis of dodoneine. Tetrahedron: Asymmetry 2009, 20, 1536-1540
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1536-1540
-
-
Das, B.1
Suneel, K.2
Satyalakshmi, G.3
Kumar, D.N.4
-
154
-
-
66249089488
-
Rationally improved chiral Brønsted acid for catalytic enantioselective allylboration of aldehydes with an expanded reagent scope
-
Rauniyar, V.; Hall, D. G. Rationally improved chiral Brønsted acid for catalytic enantioselective allylboration of aldehydes with an expanded reagent scope. J. Org. Chem. 2009, 74, 4236-4241
-
(2009)
J. Org. Chem
, vol.74
, pp. 4236-4241
-
-
Rauniyar, V.1
Hall, D.G.2
-
155
-
-
78349289572
-
Stereoselective total synthesis of dodoneine
-
Chinnababu, B.; Reddy, S. P.; Rao, C. B.; Rajesh, K.; Venkateswarlu, Y. Stereoselective total synthesis of dodoneine. Helv. Chim. Acta 2010, 93, 1960-1966.
-
(2010)
Helv. Chim. Acta
, vol.93
, pp. 1960-1966
-
-
Chinnababu, B.1
Reddy, S.P.2
Rao, C.B.3
Rajesh, K.4
Venkateswarlu, Y.5
-
156
-
-
0041350393
-
Total synthesis of (+)-strictifolione
-
BouzBouz, S.; Cossy, J. Total synthesis of (+)-strictifolione. Org. Lett. 2003, 5, 1995-1997
-
(2003)
Org. Lett
, vol.5
, pp. 1995-1997
-
-
Bouzbouz, S.1
Cossy, J.2
-
157
-
-
78650261454
-
Concise total syntheses of (+)-strictifolione and (6R)-6-[(4R,6R)-4,6-Dihydroxy-10-phenyldec-1-enyl]-5,6-dihydro-2H-pyran-2-one
-
Tang, S.; Xie, X.; Wang, X.; He, L.; Xu, K.; She, X. Concise total syntheses of (+)-strictifolione and (6R)-6-[(4R,6R)-4,6-Dihydroxy-10-phenyldec-1-enyl]-5,6-dihydro-2H-pyran-2-one. J.Org. Chem. 2010, 75, 8234-8240
-
(2010)
J.Org. Chem
, vol.75
, pp. 8234-8240
-
-
Tang, S.1
Xie, X.2
Wang, X.3
He, L.4
Xu, K.5
She, X.6
-
158
-
-
78650099772
-
Enantio-and diastereocontrolled total synthesis of (+)-strictifolione
-
Kumar, P.; Pandey, M.; Gupta, P.; Naidu, S. V.; Dhavale, D. D. Enantio-and diastereocontrolled total synthesis of (+)-strictifolione. Eur. J. Org. Chem. 2010, 6993-7004
-
(2010)
Eur. J. Org. Chem
, pp. 6993-7004
-
-
Kumar, P.1
Pandey, M.2
Gupta, P.3
Naidu, S.V.4
Dhavale, D.D.5
-
159
-
-
76649083581
-
Total synthesis of (+)-cryptocaryalactone and of a diastereoisomer of (+)-strictifolione via ring-closing metathesis (RCM) and olefin cross-metathesis
-
Sabitha, G.; Vangala, B.; Reddy, S. S. S.; Yadav, J. S. Total synthesis of (+)-cryptocaryalactone and of a diastereoisomer of (+)-strictifolione via ring-closing metathesis (RCM) and olefin cross-metathesis. Helv. Chim. Acta 2010, 93, 329-338.
-
(2010)
Helv. Chim. Acta
, vol.93
, pp. 329-338
-
-
Sabitha, G.1
Vangala, B.2
Reddy, S.S.S.3
Yadav, J.S.4
-
160
-
-
78649316926
-
An efficient synthesis of synargentolide A from D-mannitol
-
Kamal, A.; Balakrishna, M.; Reddy, P. V.; Faazil, S. An efficient synthesis of synargentolide A from D-mannitol. Tetrahedron: Asymmetry 2010, 21, 2517-2523
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2517-2523
-
-
Kamal, A.1
Balakrishna, M.2
Reddy, P.V.3
Faazil, S.4
-
161
-
-
78651399655
-
Stereoselective total synthesis of (+)-synargentolide A
-
Prasad, K. R.; Penchalaiah, K. Stereoselective total synthesis of (+)-synargentolide A. Tetrahedron: Asymmetry 2010, 21, 2853-2858
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2853-2858
-
-
Prasad, K.R.1
Penchalaiah, K.2
-
162
-
-
84864642920
-
Total synthesis of (+)-synargentolide A
-
Yadav, J. S.; Thirupathaiah, B.; Singh, V. K.; Ravishashidhar, V. Total synthesis of (+)-synargentolide A. Tetrahedron: Asymmetry 2012, 23, 931-937.
-
(2012)
Tetrahedron: Asymmetry
, vol.23
, pp. 931-937
-
-
Yadav, J.S.1
Thirupathaiah, B.2
Singh, V.K.3
Ravishashidhar, V.4
-
163
-
-
0037463510
-
Stereoselective synthesis of (+)-hyptolide
-
Murga, J.; García-Fortanet, J.; Carda, M.; Marco, J. A. Stereoselective synthesis of (+)-hyptolide. Tetrahedron Lett. 2003, 44, 1737-1739
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1737-1739
-
-
Murga, J.1
García-Fortanet, J.2
Carda, M.3
Marco, J.A.4
-
164
-
-
9644272626
-
Stereoselective synthesis of hyptolide and 6-epi-hyptolide
-
García-Fortanet, J.; Murga, J.; Carda, M.; Marco, J. A. Stereoselective synthesis of hyptolide and 6-epi-hyptolide. Tetrahedron 2004, 60, 12261-12267
-
(2004)
Tetrahedron
, vol.60
, pp. 12261-12267
-
-
García-Fortanet, J.1
Murga, J.2
Carda, M.3
Marco, J.A.4
-
166
-
-
0037433978
-
Stereoselective synthesis of spicigerolide
-
Falomir, E.; Murga, J.; Carda, M., Marco, J. A. Stereoselective synthesis of spicigerolide. Tetrahedron Lett. 2003, 44, 539-541
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 539-541
-
-
Falomir, E.1
Murga, J.2
Carda, M.3
Marco, J.A.4
-
167
-
-
0037662050
-
Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers
-
Falomir, E.; Murga, J.; Ruiz, P.; Carda, M.; Marco, J. A.; Pereda-Miranda, R.; Fragoso-Serrano, M.; Cerda-García-Rojas, C. M. Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers. J. Org. Chem. 2003, 68, 5672-5676
-
(2003)
J. Org. Chem
, vol.68
, pp. 5672-5676
-
-
Falomir, E.1
Murga, J.2
Ruiz, P.3
Carda, M.4
Marco, J.A.5
Pereda-Miranda, R.6
Fragoso-Serrano, M.7
Cerda-García-Rojas, C.M.8
-
168
-
-
64249088241
-
Stereoselective synthesis of (-)-spicigerolide
-
Georges, Y.; Ariza, X.; Garcia, J. Stereoselective synthesis of (-)-spicigerolide. J. Org. Chem. 2009, 74, 2008-2012.
-
(2009)
J. Org. Chem
, vol.74
, pp. 2008-2012
-
-
Georges, Y.1
Ariza, X.2
Garcia, J.3
-
169
-
-
1542298882
-
Stereoselective synthesis of anamarine
-
Díaz-Oltra, S.; Murga, J.; Falomir, E.; Carda, M.; Marco, J. A. Stereoselective synthesis of anamarine. Tetrahedron 2004, 60, 2979-2985
-
(2004)
Tetrahedron
, vol.60
, pp. 2979-2985
-
-
Díaz-Oltra, S.1
Murga, J.2
Falomir, E.3
Carda, M.4
Marco, J.A.5
-
170
-
-
28044447643
-
De novo asymmetric synthesis of anamarine and its analogues
-
Gao, D.; O'Doherty, G. A. De novo asymmetric synthesis of anamarine and its analogues. J. Org. Chem. 2005, 70, 9932-9939.
-
(2005)
J. Org. Chem
, vol.70
, pp. 9932-9939
-
-
Gao, D.1
O'Doherty, G.A.2
-
171
-
-
34047267475
-
Stereoselective total synthesis of (-)-synrotolide diacetate from D-ribose
-
Krishna, P. R.; Reddy, P. S. Stereoselective total synthesis of (-)-synrotolide diacetate from D-ribose. Tetrahedron 2007, 63, 3995-3999.
-
(2007)
Tetrahedron
, vol.63
, pp. 3995-3999
-
-
Krishna, P.R.1
Reddy, P.S.2
-
172
-
-
23844467556
-
Chelation-controlled reduction: An enantioselective synthesis of (-)-tarchonanthuslactone
-
Sabitha, G.; Sudhakar, K.; Reddy, N. M.; Rajkumar, M.; Yadav, J. S. Chelation-controlled reduction: an enantioselective synthesis of (-)-tarchonanthuslactone. Tetrahedron Lett. 2005, 46, 6567-6570
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 6567-6570
-
-
Sabitha, G.1
Sudhakar, K.2
Reddy, N.M.3
Rajkumar, M.4
Yadav, J.S.5
-
173
-
-
23844443275
-
Enantioselective synthesis of tarchonanthuslactone via iterative hydrolytic kinetic resolution
-
Gupta, P.; Naidu, S. V.; Kumar, P. Enantioselective synthesis of tarchonanthuslactone via iterative hydrolytic kinetic resolution. Tetrahedron Lett. 2005, 46, 6571-6573
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 6571-6573
-
-
Gupta, P.1
Naidu, S.V.2
Kumar, P.3
-
174
-
-
33846908565
-
Stereoselective synthesis of tarchonanthuslactone via the Prins cyclisation
-
Yadav, J. S.; Kumar, N. N.; Reddy, M. S.; Prasad, A R. Stereoselective synthesis of tarchonanthuslactone via the Prins cyclisation. Tetrahedron 2007, 63, 2689-2694.
-
(2007)
Tetrahedron
, vol.63
, pp. 2689-2694
-
-
Yadav, J.S.1
Kumar, N.N.2
Reddy, M.S.3
Prasad, A.R.4
-
175
-
-
0035940146
-
An enantioselective synthesis of cryptocarya diacetate
-
Hunter, T. J.; O'Doherty G. A. An enantioselective synthesis of cryptocarya diacetate. Org. Lett. 2001, 3, 2777-2780
-
(2001)
Org. Lett
, vol.3
, pp. 2777-2780
-
-
Hunter, T.J.1
O'Doherty, G.A.2
-
176
-
-
32044441817
-
A simple and efficient approach to 1,3-polyols: Application to the synthesis of cryptocarya diacetate
-
Kumar, P.; Gupta, P.; Naidu, S. V. A simple and efficient approach to 1,3-polyols: application to the synthesis of cryptocarya diacetate. Chem. Eur. J. 2006, 12, 1397-1402
-
(2006)
Chem. Eur. J
, vol.12
, pp. 1397-1402
-
-
Kumar, P.1
Gupta, P.2
Naidu, S.V.3
-
177
-
-
66949171095
-
Stereoselective routes for the total synthesis of (+)-cryptocarya diacetate
-
Sabita, G.; Reddy, N. M.; Prasad, M. N.; Yadav, J. S. Stereoselective routes for the total synthesis of (+)-cryptocarya diacetate. Helv. Chim. Acta 2009, 92, 967-976.
-
(2009)
Helv. Chim. Acta
, vol.92
, pp. 967-976
-
-
Sabita, G.1
Reddy, N.M.2
Prasad, M.N.3
Yadav, J.S.4
-
178
-
-
44749092449
-
Asymmetric synthesis of (+)-passifloricin A and its 6-epimer
-
Chandrasekhar, S.; Rambabu, C.; Reddy, A. S. Asymmetric synthesis of (+)-passifloricin A and its 6-epimer. Tetrahedron Lett. 2008, 49, 4476-4478
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 4476-4478
-
-
Chandrasekhar, S.1
Rambabu, C.2
Reddy, A.S.3
-
179
-
-
84857216714
-
Organocatalytic stereoselective synthesis of passifloricin A
-
Kumar, P.; Pandey, M.; Gupta, P.; Dhavale, D. D. Organocatalytic stereoselective synthesis of passifloricin A. Org. Biomol. Chem. 2012, 10, 1820-1825.
-
(2012)
Org. Biomol. Chem
, vol.10
, pp. 1820-1825
-
-
Kumar, P.1
Pandey, M.2
Gupta, P.3
Dhavale, D.D.4
-
180
-
-
67650326831
-
Efficient asymmetric synthesis of cryptocarya triacetate, cryptocaryolone, and cryptocaryolone diacetate
-
Wang, X.; Wang, W.; Zheng, H.; Su, Y.; Jiang, T.; He, Y.; She, X. Efficient asymmetric synthesis of cryptocarya triacetate, cryptocaryolone, and cryptocaryolone diacetate. Org. Lett. 2009, 11, 3136-3138.
-
(2009)
Org. Lett
, vol.11
, pp. 3136-3138
-
-
Wang, X.1
Wang, W.2
Zheng, H.3
Su, Y.4
Jiang, T.5
He, Y.6
She, X.7
-
181
-
-
0034108155
-
Effect of sesquiterpene lactones on antioxidant enzymes and some drug-metabolizing enzymes in rat liver and kidney
-
Jodynis-Liebert, J.; Murias, M.; Bloszyk, E. Effect of sesquiterpene lactones on antioxidant enzymes and some drug-metabolizing enzymes in rat liver and kidney. Planta Med. 2000, 66, 199-205.
-
(2000)
Planta Med
, vol.66
, pp. 199-205
-
-
Jodynis-Liebert, J.1
Murias, M.2
Bloszyk, E.3
-
182
-
-
0037149632
-
Asymmetric total synthesis of (+)-fostriecin
-
Reddy, Y. K.; Falck, J. R. Asymmetric total synthesis of (+)-fostriecin. Org. Lett. 2002, 4, 969-971
-
(2002)
Org. Lett
, vol.4
, pp. 969-971
-
-
Reddy, Y.K.1
Falck, J.R.2
-
183
-
-
0037770541
-
Formal total synthesis of fostriecin
-
Wang, Y.-G.; Kobayashi, Y. Formal total synthesis of fostriecin. Org. Lett. 2002, 4, 4615-4618
-
(2002)
Org. Lett
, vol.4
, pp. 4615-4618
-
-
Wang, Y.-G.1
Kobayashi, Y.2
-
184
-
-
0038798007
-
Formal catalytic asymmetric total synthesis of fostriecin
-
Fujii, K.; Maki, K.; Kanai, M.; Shibasaki, M. Formal catalytic asymmetric total synthesis of fostriecin. Org. Lett. 2003, 5, 733-736
-
(2003)
Org. Lett
, vol.5
, pp. 733-736
-
-
Fujii, K.1
Maki, K.2
Kanai, M.3
Shibasaki, M.4
-
185
-
-
33646117732
-
Formal synthesis of fostriecin by a carbohydrate-based approach
-
Yadav, J. S.; Prathap, I.; Tadi, B. P. Formal synthesis of fostriecin by a carbohydrate-based approach. Tetrahedron Lett. 2006, 47, 3773-3376
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 3376-3773
-
-
Yadav, J.S.1
Prathap, I.2
Tadi, B.P.3
-
186
-
-
15744395371
-
Dinuclear asymmetric Zn aldol additions: Formal asymmetric synthesis of fostriecin
-
Trost, B. M.; Frederiksen, M. U.; Papillon, J. P. N.; Harrington, P. E.; Shin, S.; Shireman, B. T. Dinuclear asymmetric Zn aldol additions: formal asymmetric synthesis of fostriecin. J. Am. Chem. Soc. 2005, 127, 3666-3667
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 3666-3667
-
-
Trost, B.M.1
Frederiksen, M.U.2
Papillon, J.P.N.3
Harrington, P.E.4
Shin, S.5
Shireman, B.T.6
-
187
-
-
28844447545
-
Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin
-
Maki, K.; Motoki, R.; Fujii, K.; Kanai, M.; Kobayashi, T.; Tamura, S., Shibasaki, M. Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin. J. Am. Chem. Soc. 2005, 127, 17111-17117
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 17111-17117
-
-
Maki, K.1
Motoki, R.2
Fujii, K.3
Kanai, M.4
Kobayashi, T.5
Tamura, S.6
Shibasaki, M.7
-
188
-
-
45849124665
-
Formal total synthesis of fostriecin via 1,4-asymmetric induction using cobalt-alkyne complex
-
Hayashi, Y.; Yamaguchi, H.; Toyoshima, M.; Okado, K.; Toyo, T.; Shoji, M. Formal total synthesis of fostriecin via 1,4-asymmetric induction using cobalt-alkyne complex. Org. Lett. 2008, 10, 1405-1408
-
(2008)
Org. Lett
, vol.10
, pp. 1405-1408
-
-
Hayashi, Y.1
Yamaguchi, H.2
Toyoshima, M.3
Okado, K.4
Toyo, T.5
Shoji, M.6
-
189
-
-
70349684843
-
Enantio-and stereoselective route to the phoslactomycin family of antibiotics: Formal synthesis of (+)-fostriecin and (+)-phoslactomycin B
-
Sarkar, S. M.; Wanzala, E. N.; Shibahara, S.; Takahashi, K.; Ishihara, J.; Hatakeyama, S. Enantio-and stereoselective route to the phoslactomycin family of antibiotics: formal synthesis of (+)-fostriecin and (+)-phoslactomycin B. Chem. Comm. 2009, 5907-5909
-
(2009)
Chem. Comm
, pp. 5907-5909
-
-
Sarkar, S.M.1
Wanzala, E.N.2
Shibahara, S.3
Takahashi, K.4
Ishihara, J.5
Hatakeyama, S.6
-
190
-
-
70449440706
-
Total synthesis of (+)-fostriecin and (+)-phoslactomycin B
-
Shibahara, S.; Fujino, M.; Tashiro, Y.; Okamoto, N.; Esumi, T.; Takahashi, K.; Ishihara, J.; Hakateyama, S. Total synthesis of (+)-fostriecin and (+)-phoslactomycin B. Synthesis 2009, 2935-2953.
-
(2009)
Synthesis
, pp. 2935-2953
-
-
Shibahara, S.1
Fujino, M.2
Tashiro, Y.3
Okamoto, N.4
Esumi, T.5
Takahashi, K.6
Ishihara, J.7
Hakateyama, S.8
-
191
-
-
77956196503
-
Total synthesis of fostriecin: Via a regioand stereoselective polyene hydration, oxidation, and hydroboration sequence
-
Gao, D.; O'Doherty, G.A. Total synthesis of fostriecin: via a regioand stereoselective polyene hydration, oxidation, and hydroboration sequence. Org. Lett. 2010, 12, 3752-3755.
-
(2010)
Org. Lett
, vol.12
, pp. 3752-3755
-
-
Gao, D.1
O'Doherty, G.A.2
-
192
-
-
77956103357
-
Formal total synthesis of fostriecin by 1,4-asymmetric induction with an alkyne-cobalt complex
-
Hayashi, Y.; Yamaguchi, H.; Toyoshima, M.; Okado, K.; Toyo, T.; Shoji, M. Formal total synthesis of fostriecin by 1,4-asymmetric induction with an alkyne-cobalt complex. Chem. Eur. J. 2010, 16, 10150-10159.
-
(2010)
Chem. Eur. J
, vol.16
, pp. 10150-10159
-
-
Hayashi, Y.1
Yamaguchi, H.2
Toyoshima, M.3
Okado, K.4
Toyo, T.5
Shoji, M.6
-
193
-
-
33845928989
-
Total synthesis and evaluation of cytostatin, its C10-C11 diastereomers, and additional key analogues: Impact on PP2A inhibition
-
Lawhorn, B. G.; Boga, S. B.; Wolkenberg, S. E.; Colby, D. A.; Gauss, C.-M.; Swingle, M. R.; Amable, L.; Honkanen, R. E.; Boger, D. L. Total synthesis and evaluation of cytostatin, its C10-C11 diastereomers, and additional key analogues: impact on PP2A inhibition. J. Am. Chem. Soc. 2006, 128, 16720-16732
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 16720-16732
-
-
Lawhorn, B.G.1
Boga, S.B.2
Wolkenberg, S.E.3
Colby, D.A.4
Gauss, C.-M.5
Swingle, M.R.6
Amable, L.7
Honkanen, R.E.8
Boger, D.L.9
-
194
-
-
45449118689
-
Synthetic studies toward cytostatin, a natural product inhibitor of protein phosphatase 2A
-
Salit, A.-F.; Meyer, C.; Cossy, J.; Delouvrié, B.; Hennequin, L. Synthetic studies toward cytostatin, a natural product inhibitor of protein phosphatase 2A. Tetrahedron 2008, 64, 6684-6697.
-
(2008)
Tetrahedron
, vol.64
, pp. 6684-6697
-
-
Salit, A.-F.1
Meyer, C.2
Cossy, J.3
Delouvrié, B.4
Hennequin, L.5
-
195
-
-
52649178941
-
Asymmetric total synthesis of (+)-phoslactomycin B
-
Shibahara, S; Fujino, M.; Tashiro, Y.; Takahashi, K.; Ishihara, J.; Hakateyama, S. Asymmetric total synthesis of (+)-phoslactomycin B. Org. Lett. 2008, 10, 2139-2142
-
(2008)
Org. Lett
, vol.10
, pp. 2139-2142
-
-
Shibahara, S.1
Fujino, M.2
Tashiro, Y.3
Takahashi, K.4
Ishihara, J.5
Hakateyama, S.6
-
196
-
-
62749144066
-
A convergent approach toward the C1-C11 subunit of phoslactomycins and formal synthesis of phoslactomycin B
-
Druais, V.; Hall, M. J.; Corsi, C.; Wendeborn, S. V.; Meyer, C.; Cossy, J. A convergent approach toward the C1-C11 subunit of phoslactomycins and formal synthesis of phoslactomycin B. Org. Lett. 2009, 11, 935-938
-
(2009)
Org. Lett
, vol.11
, pp. 935-938
-
-
Druais, V.1
Hall, M.J.2
Corsi, C.3
Wendeborn, S.V.4
Meyer, C.5
Cossy, J.6
-
197
-
-
77955655685
-
A convergent approach toward phoslactomycins and leustroducsins
-
Druais, V.; Hall, M. J.; Corsi, C.; Wendeborn, S. V.; Meyer, C.; Cossy, J. A convergent approach toward phoslactomycins and leustroducsins. Tetrahedron 2010, 66, 6358-6375.
-
(2010)
Tetrahedron
, vol.66
, pp. 6358-6375
-
-
Druais, V.1
Hall, M.J.2
Corsi, C.3
Wendeborn, S.V.4
Meyer, C.5
Cossy, J.6
-
198
-
-
79958828859
-
Formal synthesis of leustroducsin B via Reformatsky/Claisen condensation of silyl glyoxylates
-
Greszler, S. N.; Malinowsky, J. T.; Johnson, J. S. Formal synthesis of leustroducsin B via Reformatsky/Claisen condensation of silyl glyoxylates. Org. Lett. 2011, 13, 3206-3209.
-
(2011)
Org. Lett
, vol.13
, pp. 3206-3209
-
-
Greszler, S.N.1
Malinowsky, J.T.2
Johnson, J.S.3
-
199
-
-
34250374307
-
Asymmetric total synthesis of (-)-pironetin employing the SAMP/RAMP hydrazone methodology
-
Enders, D.; Dhulut, S.; Steinbusch, D.; Herrbach, A. Asymmetric total synthesis of (-)-pironetin employing the SAMP/RAMP hydrazone methodology. Chem. Eur. J. 2007, 13, 3942-3949
-
(2007)
Chem. Eur. J
, vol.13
, pp. 3942-3949
-
-
Enders, D.1
Dhulut, S.2
Steinbusch, D.3
Herrbach, A.4
-
200
-
-
57749097109
-
Asymmetric total synthesis of the immunosuppressant (-)-pironetin
-
Bressy, C.; Vors, J.-P.; Hillebrand, S.; Arseniyadis, S.; Cossy, J. Asymmetric total synthesis of the immunosuppressant (-)-pironetin. Angew. Chem. Int. Ed. 2008, 47, 10137-10140.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 10137-10140
-
-
Bressy, C.1
Vors, J.-P.2
Hillebrand, S.3
Arseniyadis, S.4
Cossy, J.5
-
201
-
-
43649104068
-
Total synthesis of (+)-asperlin
-
Akaike, H.; Horie, H.; Kato, K.; Akita, H. Total synthesis of (+)-asperlin. Tetrahedron: Asymmetry 2008, 19, 1100-1105.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 1100-1105
-
-
Akaike, H.1
Horie, H.2
Kato, K.3
Akita, H.4
-
202
-
-
77950332380
-
Total synthesis of (-)-cleistenolide
-
Schmidt, B.; Kunz, O.; Biernat, A. Total synthesis of (-)-cleistenolide. J. Org. Chem. 2010, 75, 2389-2394
-
(2010)
J. Org. Chem
, vol.75
, pp. 2389-2394
-
-
Schmidt, B.1
Kunz, O.2
Biernat, A.3
-
203
-
-
79953737878
-
Total synthesis of (-)-cleistenolide
-
Ramesh, P.; Meshram, H. M. Total synthesis of (-)-cleistenolide. Tetrahedron Lett. 2011, 52, 2443-2445
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 2443-2445
-
-
Ramesh, P.1
Meshram, H.M.2
-
204
-
-
79955658942
-
Stereoselective total synthesis of (-)-cleistenolide
-
Babu, D. C.; Selavam, J. J. P.; Reddy, D. K.; Shekhar, V.; Venkateswarlu, Y. Stereoselective total synthesis of (-)-cleistenolide. Tetrahedron 2011, 67, 3815-3819.
-
(2011)
Tetrahedron
, vol.67
, pp. 3815-3819
-
-
Babu, D.C.1
Selavam, J.J.P.2
Reddy, D.K.3
Shekhar, V.4
Venkateswarlu, Y.5
-
205
-
-
80054972796
-
First stereoselective total synthesis of pectinolide A
-
Yadav, J. S.; Mandal, S. S. First stereoselective total synthesis of pectinolide A. Tetrahedron Lett. 2011, 52, 5747-5749.
-
(2011)
Tetrahedron Lett
, vol.52
, pp. 5747-5749
-
-
Yadav, J.S.1
Mandal, S.S.2
-
206
-
-
79956118597
-
Synthesis of (+)-dumetorine and congeners by using flow chemistry technologies
-
Riva, E.; Rencurosi, A.; Gagliardi, S.; Passarella, D.; Martinelli, M. Synthesis of (+)-dumetorine and congeners by using flow chemistry technologies. Chem. Eur. J. 2011, 17, 6221-6226.
-
(2011)
Chem. Eur. J
, vol.17
, pp. 6221-6226
-
-
Riva, E.1
Rencurosi, A.2
Gagliardi, S.3
Passarella, D.4
Martinelli, M.5
-
207
-
-
56449120599
-
Structure and absolute stereochemistry of the anticancer agent EBC-23 from the Australian rainforest
-
Dong, L.; Gordon, V. A.; Grange, R. L.; Johns, J.; Parsons, P. G.; Porzelle, A.; Reddell, P.; Schill, H.; Williams, C. M. Structure and absolute stereochemistry of the anticancer agent EBC-23 from the Australian rainforest. J. Am. Chem. Soc. 2008, 130, 15262-15263
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 15262-15263
-
-
Dong, L.1
Gordon, V.A.2
Grange, R.L.3
Johns, J.4
Parsons, P.G.5
Porzelle, A.6
Reddell, P.7
Schill, H.8
Williams, C.M.9
-
208
-
-
70350515497
-
Anticancer agents from the Australian tropical rainforest: Spiroacetals EBC-23, 24, 25, 72, 73, 75 and 76
-
Dong, L.; Schill, H.; Grange, R. L.; Porzelle, A.; Johns, J. P.; Parsons, P. G.; Gordon, V. A.; Reddell, P. W., Williams, C. M. Anticancer agents from the Australian tropical rainforest: spiroacetals EBC-23, 24, 25, 72, 73, 75 and 76. Chem. Eur. J. 2009, 15, 11307-11318.
-
(2009)
Chem. Eur. J
, vol.15
, pp. 11307-11318
-
-
Dong, L.1
Schill, H.2
Grange, R.L.3
Porzelle, A.4
Johns, J.P.5
Parsons, P.G.6
Gordon, V.A.7
Reddell, P.W.8
Williams, C.M.9
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