-
1
-
-
0001147462
-
Cycloaddition Reactions in Organic Synthesis
-
Baldwin, J. E. Magnus, P. D. Pergamon: Oxford, UK
-
Carruthers, W. Cycloaddition Reactions in Organic Synthesis. In Tetrahedron Organic Chemistry Series; Baldwin, J. E., Magnus, P. D., Eds.; Pergamon: Oxford, UK, 1990; Vol. 8; pp 1-373.
-
(1990)
Tetrahedron Organic Chemistry Series
, vol.8
, pp. 1-373
-
-
Carruthers, W.1
-
3
-
-
84897531244
-
-
Tebby, J. C. John Wiley & Sons Ltd. Chichester, UK.
-
Alexandrovna, M. I.; Ionin, B. I. Alkynes in Cycloadditions; Tebby, J. C., Ed.; John Wiley & Sons Ltd.: Chichester, UK, 2014.
-
(2014)
Alkynes in Cycloadditions
-
-
Alexandrovna, M.I.1
Ionin, B.I.2
-
4
-
-
84893838561
-
Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis
-
Nawrat, C. C.; Moody, C. J. Quinones as Dienophiles in the Diels-Alder Reaction: History and Applications in Total Synthesis Angew. Chem., Int. Ed. 2014, 53, 2056-2077
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 2056-2077
-
-
Nawrat, C.C.1
Moody, C.J.2
-
5
-
-
84875695231
-
Industrial Applications of the Diels-Alder Reaction
-
Funel, J.-A.; Abele, S. Industrial Applications of the Diels-Alder Reaction Angew. Chem., Int. Ed. 2013, 52, 3822-3863
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 3822-3863
-
-
Funel, J.-A.1
Abele, S.2
-
6
-
-
84874818666
-
Diels-Alder Reactions in the Synthesis of Higher Terpenes
-
Hudlicky, T. Elsevier Science Ltd. Oxford, UK
-
Brocksom, T. J.; Corrêa, A. G.; Naves, R. M.; Silva, F., Jr.; Catani, V.; Ceschi, M. A.; Zukerman-Schpector, J.; Toloi, A. P.; Ferreira, M. L.; Brocksom, U. Diels-Alder Reactions in the Synthesis of Higher Terpenes. In Organic Synthesis: Theory and Applications; Hudlicky, T., Ed.; Elsevier Science Ltd.: Oxford, UK, 2001; Vol. 5, pp 39-87.
-
(2001)
Organic Synthesis: Theory and Applications
, vol.5
, pp. 39-87
-
-
Brocksom, T.J.1
Corrêa, A.G.2
Naves, R.M.3
Silva, F.4
Catani, V.5
Ceschi, M.A.6
Zukerman-Schpector, J.7
Toloi, A.P.8
Ferreira, M.L.9
Brocksom, U.10
-
7
-
-
30744456747
-
Recent Advances in Natural Product Synthesis by Using Intramolecular Diels-Alder Reactions
-
Takao, K.-i.; Munakata, R.; Tadano, K.-i. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels-Alder Reactions Chem. Rev. 2005, 105, 4779-4806
-
(2005)
Chem. Rev.
, vol.105
, pp. 4779-4806
-
-
Takao, K.-I.1
Munakata, R.2
Tadano, K.-I.3
-
8
-
-
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
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 1668-1698
-
-
Nicolaou, K.C.1
Snyder, S.A.2
Montagnon, T.3
Vassilikogiannakis, G.4
-
9
-
-
4243599124
-
Progress in the Diels-Alder Reaction Means Progress in Steroid Synthesis
-
Ottow, E. Schollkopf, K. Schulz, B. G. Springer-Verlag: Berlin.
-
Quinkert, G.; del Grosso, M. Progress in the Diels-Alder Reaction Means Progress in Steroid Synthesis. In Stereoselective Synthesis; Ottow, E.; Schollkopf, K.; Schulz, B. G., Eds.; Springer-Verlag: Berlin, 1994.
-
(1994)
Stereoselective Synthesis
-
-
Quinkert, G.1
Del Grosso, M.2
-
10
-
-
70350496831
-
Recent Applications of Intramolecular Diels-Alder Reactions to Natural Product Synthesis
-
Juhl, M.; Tanner, D. Recent Applications of Intramolecular Diels-Alder Reactions to Natural Product Synthesis Chem. Soc. Rev. 2009, 38, 2983-2992
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 2983-2992
-
-
Juhl, M.1
Tanner, D.2
-
11
-
-
0003667457
-
-
ACS Monograph 180; American Chemical Society: Washington, DC.
-
[4 + 2]-Cycloadditions in Natural Products Synthesis Through Pericyclic Reactions; Desimoni, G.; Tacconi, G.; Barco, A.; Pollini, G. P. ACS Monograph 180; American Chemical Society: Washington, DC, 1983.
-
(1983)
[4 + 2]-Cycloadditions in Natural Products Synthesis Through Pericyclic Reactions
-
-
Desimoni, G.1
Tacconi, G.2
Barco, A.3
Pollini, G.P.4
-
12
-
-
84962105974
-
Synthesen in der Hydroaromatischen Reihe
-
Diels, O.; Alder, K. Synthesen in Der Hydroaromatischen Reihe Justus Liebigs Ann. Chem. 1928, 460, 98-122
-
(1928)
Justus Liebigs Ann. Chem.
, vol.460
, pp. 98-122
-
-
Diels, O.1
Alder, K.2
-
14
-
-
0039930587
-
Acceleration and Selectivity Enhancement of Diels-Alder Reactions by Special and Catalytic Methods
-
Pindur, U.; Lutz, G.; Otto, C. Acceleration and Selectivity Enhancement of Diels-Alder Reactions by Special and Catalytic Methods Chem. Rev. 1993, 93, 741-761
-
(1993)
Chem. Rev.
, vol.93
, pp. 741-761
-
-
Pindur, U.1
Lutz, G.2
Otto, C.3
-
15
-
-
84880100773
-
Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels-Alder Reaction
-
Jiang, X.; Wang, R. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels-Alder Reaction Chem. Rev. 2013, 113, 5515-5546
-
(2013)
Chem. Rev.
, vol.113
, pp. 5515-5546
-
-
Jiang, X.1
Wang, R.2
-
16
-
-
0030963855
-
RNA-Catalysed Carbon-Carbon Bond Formation
-
Tarasow, T. M.; Tarasow, S. L.; Eaton, B. E. RNA-Catalysed Carbon-Carbon Bond Formation Nature 1997, 389, 54-57
-
(1997)
Nature
, vol.389
, pp. 54-57
-
-
Tarasow, T.M.1
Tarasow, S.L.2
Eaton, B.E.3
-
17
-
-
0035804164
-
Diels-Alderases
-
Pohnert, G. Diels-Alderases ChemBioChem 2001, 2, 873-875
-
(2001)
ChemBioChem
, vol.2
, pp. 873-875
-
-
Pohnert, G.1
-
18
-
-
0033618847
-
The Diels-Alder Reaction and Biopolymer Catalysis
-
Tarasow, T. M.; Eaton, B. E. The Diels-Alder Reaction and Biopolymer Catalysis Cell. Mol. Life Sci. 1999, 55, 1463-1472
-
(1999)
Cell. Mol. Life Sci.
, vol.55
, pp. 1463-1472
-
-
Tarasow, T.M.1
Eaton, B.E.2
-
19
-
-
0033102314
-
A Small Catalytic RNA Motif with Diels-Alderase Activity
-
Seelig, B.; Jäschke, A. A Small Catalytic RNA Motif with Diels-Alderase Activity Chem. Biol. 1999, 6, 167-176
-
(1999)
Chem. Biol.
, vol.6
, pp. 167-176
-
-
Seelig, B.1
Jäschke, A.2
-
20
-
-
0033594331
-
Characteristics of an RNA Diels-Alderase Active Site
-
Tarasow, T. M.; Tarasow, S. L.; Tu, C.; Kellogg, E.; Eaton, B. E. Characteristics of an RNA Diels-Alderase Active Site J. Am. Chem. Soc. 1999, 121, 3614-3617
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 3614-3617
-
-
Tarasow, T.M.1
Tarasow, S.L.2
Tu, C.3
Kellogg, E.4
Eaton, B.E.5
-
21
-
-
0034671737
-
Enantioselective Ribozyme Catalysis of a Bimolecular Cycloaddition Reaction
-
Seelig, B.; Keiper, S.; Stuhlmann, F.; Jäschke, A. Enantioselective Ribozyme Catalysis of a Bimolecular Cycloaddition Reaction Angew. Chem., Int. Ed. 2000, 39, 4576-4579
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 4576-4579
-
-
Seelig, B.1
Keiper, S.2
Stuhlmann, F.3
Jäschke, A.4
-
22
-
-
23044436253
-
Allosterically Activated Diels-Alder Catalysis by a Ribozyme
-
Helm, M.; Petermeier, M.; Ge, B.; Fiammengo, R.; Jäschke, A. Allosterically Activated Diels-Alder Catalysis by a Ribozyme J. Am. Chem. Soc. 2005, 127, 10492-10493
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10492-10493
-
-
Helm, M.1
Petermeier, M.2
Ge, B.3
Fiammengo, R.4
Jäschke, A.5
-
23
-
-
41449109957
-
DNA and RNA can be Equally Efficient Catalysts for Carbon-Carbon Bond Formation
-
Chandra, M.; Silverman, S. K. DNA and RNA can be Equally Efficient Catalysts for Carbon-Carbon Bond Formation J. Am. Chem. Soc. 2008, 130, 2936-2937
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 2936-2937
-
-
Chandra, M.1
Silverman, S.K.2
-
24
-
-
84929210482
-
RNA as a Catalyst: The Diels-Alderase Ribozyme
-
Schmuck, C. Wennemers, H. Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany.
-
Keiper, S.; Bebenroth, D.; Stuhlmann, F.; Jäschke, A. RNA as a Catalyst: The Diels-Alderase Ribozyme. In Highlights in Bioorganic Chemistry: Methods and Applications; Schmuck, C.; Wennemers, H., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2005.
-
(2005)
Highlights in Bioorganic Chemistry: Methods and Applications
-
-
Keiper, S.1
Bebenroth, D.2
Stuhlmann, F.3
Jäschke, A.4
-
25
-
-
84886145796
-
RNA as a Catalyst: The Diels-Alderase Ribozyme
-
Mayer, G. John Wiley & Sons, Ltd. Chichester, UK.
-
Jäschke, A. RNA as a Catalyst: The Diels-Alderase Ribozyme. In The Chemical Biology of Nucleic Acids; Mayer, G., Ed.; John Wiley & Sons, Ltd.: Chichester, UK, 2010.
-
(2010)
The Chemical Biology of Nucleic Acids
-
-
Jäschke, A.1
-
26
-
-
0342974220
-
Transannular Diels-Alder Reaction on Macrocycles. A General Strategy for the Synthesis of Polycyclic Compounds
-
Deslongchamps, P. Transannular Diels-Alder Reaction on Macrocycles. A General Strategy for the Synthesis of Polycyclic Compounds Pure Appl. Chem. 1992, 64, 1831-1847
-
(1992)
Pure Appl. Chem.
, vol.64
, pp. 1831-1847
-
-
Deslongchamps, P.1
-
27
-
-
0035858717
-
The Transannular Diels-Alder Strategy: Applications to Total Synthesis
-
Marsault, E.; Toró, A.; Nowak, P.; Deslongchamps, P. The Transannular Diels-Alder Strategy: Applications to Total Synthesis Tetrahedron 2001, 57, 4243-4260
-
(2001)
Tetrahedron
, vol.57
, pp. 4243-4260
-
-
Marsault, E.1
Toró, A.2
Nowak, P.3
Deslongchamps, P.4
-
28
-
-
34648829990
-
Asymmetric Catalysis of the Transannular Diels-Alder Reaction
-
Balskus, E. P.; Jacobsen, E. N. Asymmetric Catalysis of the Transannular Diels-Alder Reaction Science 2007, 317, 1736-1740
-
(2007)
Science
, vol.317
, pp. 1736-1740
-
-
Balskus, E.P.1
Jacobsen, E.N.2
-
29
-
-
77957900964
-
Synthesis of a trans, syn, trans-Dodecahydrophenanthrene via a Bicyclic Transannular Diels-Alder Reaction: Intermediate for the Synthesis of Fusidic Acid
-
Jung, M. E.; Zhang, T.-H.; Lui, R. M.; Gutierrez, O.; Houk, K. N. Synthesis of a trans, syn, trans-Dodecahydrophenanthrene via a Bicyclic Transannular Diels-Alder Reaction: Intermediate for the Synthesis of Fusidic Acid J. Org. Chem. 2010, 75, 6933-6940
-
(2010)
J. Org. Chem.
, vol.75
, pp. 6933-6940
-
-
Jung, M.E.1
Zhang, T.-H.2
Lui, R.M.3
Gutierrez, O.4
Houk, K.N.5
-
30
-
-
84862562467
-
Transannular Diels-Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study
-
Prathyusha, V.; Ramakrishna, S.; Deva Priyakumar, U. Transannular Diels-Alder Reactivities of 14-Membered Macrocylic Trienes and Their Relationship with the Conformational Preferences of the Reactants: A Combined Quantum Chemical and Molecular Dynamics Study J. Org. Chem. 2012, 77, 5371-5380
-
(2012)
J. Org. Chem.
, vol.77
, pp. 5371-5380
-
-
Prathyusha, V.1
Ramakrishna, S.2
Deva Priyakumar, U.3
-
31
-
-
84873325401
-
Increasing the Efficiency of the Transannular Diels-Alder Strategy via Palladium(II)-Catalyzed Macrocyclizations
-
Iafe, R. G.; Kuo, J. L.; Hochstatter, D. G.; Saga, T.; Turner, J. W.; Merlic, C. A. Increasing the Efficiency of the Transannular Diels-Alder Strategy via Palladium(II)-Catalyzed Macrocyclizations Org. Lett. 2013, 15, 582-585
-
(2013)
Org. Lett.
, vol.15
, pp. 582-585
-
-
Iafe, R.G.1
Kuo, J.L.2
Hochstatter, D.G.3
Saga, T.4
Turner, J.W.5
Merlic, C.A.6
-
32
-
-
84886305653
-
Transannular Diels-Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues
-
Campbell, E. L.; Skepper, C. K.; Sankar, K.; Duncan, K. K.; Boger, D. L. Transannular Diels-Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Total Synthesis of a Unique Set of Vinblastine Analogues Org. Lett. 2013, 15, 5306-5309
-
(2013)
Org. Lett.
, vol.15
, pp. 5306-5309
-
-
Campbell, E.L.1
Skepper, C.K.2
Sankar, K.3
Duncan, K.K.4
Boger, D.L.5
-
33
-
-
47249130867
-
The Dehydro-Diels-Alder Reaction
-
Wessig, P.; Müller, G. The Dehydro-Diels-Alder Reaction Chem. Rev. 2008, 108, 2051-2063
-
(2008)
Chem. Rev.
, vol.108
, pp. 2051-2063
-
-
Wessig, P.1
Müller, G.2
-
34
-
-
80055020011
-
The Photo-Dehydro-Diels-Alder (PDDA) Reaction
-
Wessig, P.; Matthes, A.; Pick, C. The Photo-Dehydro-Diels-Alder (PDDA) Reaction Org. Biomol. Chem. 2011, 9, 7599-7605
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 7599-7605
-
-
Wessig, P.1
Matthes, A.2
Pick, C.3
-
35
-
-
84895922525
-
Base-Catalyzed Tandem Michael/Dehydro-Diels-Alder Reaction of α,α-Dicyanoolefins with Electron-Deficient 1,3-Conjugated Enynes: A Facile Entry to Angularly Fused Polycycles
-
Zhang, M.; Zhang, J. Base-Catalyzed Tandem Michael/Dehydro-Diels-Alder Reaction of α,α-Dicyanoolefins with Electron-Deficient 1,3-Conjugated Enynes: A Facile Entry to Angularly Fused Polycycles Chem. - Eur. J. 2014, 20, 399-404
-
(2014)
Chem. - Eur. J.
, vol.20
, pp. 399-404
-
-
Zhang, M.1
Zhang, J.2
-
36
-
-
84866034566
-
A Thermal Dehydrogenative Diels-Alder Reaction of Styrenes for the Concise Synthesis of Functionalized Naphthalenes
-
Kocsis, L. S.; Benedetti, E.; Brummond, K. M. A Thermal Dehydrogenative Diels-Alder Reaction of Styrenes for the Concise Synthesis of Functionalized Naphthalenes Org. Lett. 2012, 14, 4430-4433
-
(2012)
Org. Lett.
, vol.14
, pp. 4430-4433
-
-
Kocsis, L.S.1
Benedetti, E.2
Brummond, K.M.3
-
37
-
-
0030724760
-
Thermolysis of 1,3,8-Nonatriyne: Evidence for Intramolecular [2 + 4] Cycloaromatization to a Benzyne Intermediate
-
Bradley, A. Z.; Johnson, R. P. Thermolysis of 1,3,8-Nonatriyne: Evidence for Intramolecular [2 + 4] Cycloaromatization to a Benzyne Intermediate J. Am. Chem. Soc. 1997, 119, 9917-9918
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 9917-9918
-
-
Bradley, A.Z.1
Johnson, R.P.2
-
38
-
-
69949112734
-
A Metal-Templated 4 + 2 Cycloaddition Reaction of an Alkyne and a Diyne to Form a 1,2-Aryne
-
Tsui, J. A.; Sterenberg, B. T. A Metal-Templated 4 + 2 Cycloaddition Reaction of an Alkyne and a Diyne To Form a 1,2-Aryne Organometallics 2009, 28, 4906-4908
-
(2009)
Organometallics
, vol.28
, pp. 4906-4908
-
-
Tsui, J.A.1
Sterenberg, B.T.2
-
39
-
-
84867327958
-
The Hexadehydro-Diels-Alder Reaction
-
Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. The Hexadehydro-Diels-Alder Reaction Nature 2012, 490, 208-212
-
(2012)
Nature
, vol.490
, pp. 208-212
-
-
Hoye, T.R.1
Baire, B.2
Niu, D.3
Willoughby, P.H.4
Woods, B.P.5
-
40
-
-
84875172314
-
Synthesis of Complex Benzenoids via the Intermediate Generation of o -Benzynes Through the Hexadehydro-Diels-Alder Reaction
-
Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P.; Hoye, T. R. Synthesis of Complex Benzenoids via the Intermediate Generation of o -Benzynes Through the Hexadehydro-Diels-Alder Reaction Nat. Protoc. 2013, 8, 501-508
-
(2013)
Nat. Protoc.
, vol.8
, pp. 501-508
-
-
Baire, B.1
Niu, D.2
Willoughby, P.H.3
Woods, B.P.4
Hoye, T.R.5
-
41
-
-
84876557127
-
Alder-Ene Reactions of Arynes
-
Karmakar, R.; Mamidipalli, P.; Yun, S. Y.; Lee, D. Alder-Ene Reactions of Arynes Org. Lett. 2013, 15, 1938-1941
-
(2013)
Org. Lett.
, vol.15
, pp. 1938-1941
-
-
Karmakar, R.1
Mamidipalli, P.2
Yun, S.Y.3
Lee, D.4
-
42
-
-
84891800470
-
Regioselectivity in the Nucleophile Trapping of Arynes: The Electronic and Steric Effects of Nucleophiles and Substituents
-
Karmakar, R.; Yun, S. Y.; Wang, K.-P.; Lee, D. Regioselectivity in the Nucleophile Trapping of Arynes: The Electronic and Steric Effects of Nucleophiles and Substituents Org. Lett. 2014, 16, 6-9
-
(2014)
Org. Lett.
, vol.16
, pp. 6-9
-
-
Karmakar, R.1
Yun, S.Y.2
Wang, K.-P.3
Lee, D.4
-
43
-
-
84891791022
-
Dichlorination of (Hexadehydro-Diels-Alder Generated) Benzynes and a Protocol for Interrogating the Kinetic Order of Bimolecular Aryne Trapping Reactions
-
Niu, D.; Wang, T.; Woods, B. P.; Hoye, T. R. Dichlorination of (Hexadehydro-Diels-Alder Generated) Benzynes and a Protocol for Interrogating the Kinetic Order of Bimolecular Aryne Trapping Reactions Org. Lett. 2014, 16, 254-257
-
(2014)
Org. Lett.
, vol.16
, pp. 254-257
-
-
Niu, D.1
Wang, T.2
Woods, B.P.3
Hoye, T.R.4
-
44
-
-
84901782644
-
The Hexadehydro-Diels-Alder Reaction: A New Chapter in Aryne Chemistry
-
Holden (née Hall), C.; Greaney, M. F. The Hexadehydro-Diels-Alder Reaction: A New Chapter in Aryne Chemistry Angew. Chem., Int. Ed. 2014, 53, 5746-5749
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 5746-5749
-
-
Holden, C.1
Greaney, M.F.2
-
45
-
-
33748216380
-
Photo-induced exo-Selective Diels-Alder Reactions
-
Pandey, B.; Dalvi, P. V. Photo-induced exo-Selective Diels-Alder Reactions Angew. Chem., Int. Ed. Engl. 1993, 32, 1612-1613
-
(1993)
Angew. Chem., Int. Ed. Engl.
, vol.32
, pp. 1612-1613
-
-
Pandey, B.1
Dalvi, P.V.2
-
46
-
-
55449123606
-
Exo- and Enantioselective Diels-Alder Reactions: Pyrazolidinone Auxiliaries as a Means to Enhanced Exo Selectivity
-
Sibi, M. P.; Nie, X.; Shackleford, J. P.; Stanley, L. M.; Bouret, F. Exo- and Enantioselective Diels-Alder Reactions: Pyrazolidinone Auxiliaries as a Means to Enhanced Exo Selectivity Synlett 2008, 2655-2658
-
(2008)
Synlett
, pp. 2655-2658
-
-
Sibi, M.P.1
Nie, X.2
Shackleford, J.P.3
Stanley, L.M.4
Bouret, F.5
-
47
-
-
34548592016
-
Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts
-
Kano, T.; Tanaka, Y.; Maruoka, K. Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts Chem. - Asian J. 2007, 2, 1161-1165
-
(2007)
Chem. - Asian J.
, vol.2
, pp. 1161-1165
-
-
Kano, T.1
Tanaka, Y.2
Maruoka, K.3
-
48
-
-
80052455391
-
Exo-Selective Asymmetric Diels-Alder Reaction of 2,4-Dienals and Nitroalkenes by Trienamine Catalysis
-
Jia, Z.-J.; Zhou, Q.; Zhou, Q.-Q.; Chen, P.-Q.; Chen, Y.-C. Exo-Selective Asymmetric Diels-Alder Reaction of 2,4-Dienals and Nitroalkenes by Trienamine Catalysis Angew. Chem., Int. Ed. 2011, 50, 8638-8641
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 8638-8641
-
-
Jia, Z.-J.1
Zhou, Q.2
Zhou, Q.-Q.3
Chen, P.-Q.4
Chen, Y.-C.5
-
49
-
-
34547149552
-
Diarylprolinol Silyl Ether as Catalyst of an exo-Selective, Enantioselective Diels-Alder Reaction
-
Gotoh, H.; Hayashi, Y. Diarylprolinol Silyl Ether as Catalyst of an exo-Selective, Enantioselective Diels-Alder Reaction Org. Lett. 2007, 9, 2859-2862
-
(2007)
Org. Lett.
, vol.9
, pp. 2859-2862
-
-
Gotoh, H.1
Hayashi, Y.2
-
50
-
-
33746125825
-
Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts
-
Kano, T.; Tanaka, Y.; Maruoka, K. Exo-Selective Asymmetric Diels-Alder Reaction Catalyzed by Diamine Salts as Organocatalysts Org. Lett. 2006, 8, 2687-2689
-
(2006)
Org. Lett.
, vol.8
, pp. 2687-2689
-
-
Kano, T.1
Tanaka, Y.2
Maruoka, K.3
-
51
-
-
0001284159
-
Exo-Selective Diels-Alder Reaction Based on a Molecular Recognition Approach
-
Maruoka, K.; Imoto, H.; Yamamoto, H. Exo-Selective Diels-Alder Reaction Based on a Molecular Recognition Approach J. Am. Chem. Soc. 1994, 116, 12115-12116
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 12115-12116
-
-
Maruoka, K.1
Imoto, H.2
Yamamoto, H.3
-
52
-
-
0003104696
-
Exo-Selective Diels-Alder Reaction of Nitroolefins with Danishefsky's Diene
-
Node, M.; Nishide, K.; Imazato, H.; Kurosaki, R.; Inoue, T.; Ikariya, T. Exo-Selective Diels-Alder Reaction of Nitroolefins with Danishefsky's Diene Chem. Commun. 1996, 2559-2560
-
(1996)
Chem. Commun.
, pp. 2559-2560
-
-
Node, M.1
Nishide, K.2
Imazato, H.3
Kurosaki, R.4
Inoue, T.5
Ikariya, T.6
-
53
-
-
0030748044
-
Asymmetric Exo-Selective Diels-Alder Reactions by Steric Attenuation of Secondary Orbital Interactions
-
Powers, T. S.; Jiang, W.; Su, J.; Wulff, W. D.; Waltermire, B. E.; Rheingold, A. L. Asymmetric Exo-Selective Diels-Alder Reactions by Steric Attenuation of Secondary Orbital Interactions J. Am. Chem. Soc. 1997, 119, 6438-6439
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 6438-6439
-
-
Powers, T.S.1
Jiang, W.2
Su, J.3
Wulff, W.D.4
Waltermire, B.E.5
Rheingold, A.L.6
-
54
-
-
67849083450
-
Diels-Alder Exo Selectivity in Terminal-Substituted Dienes and Dienophiles: Experimental Discoveries and Computational Explanations
-
Lam, Y.-H.; Cheong, P. H.-Y.; Blasco Mata, J. M.; Stanway, S. J.; Gouverneur, V.; Houk, K. N. Diels-Alder Exo Selectivity in Terminal-Substituted Dienes and Dienophiles: Experimental Discoveries and Computational Explanations J. Am. Chem. Soc. 2009, 131, 1947-1957
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 1947-1957
-
-
Lam, Y.-H.1
Cheong, P.H.-Y.2
Blasco Mata, J.M.3
Stanway, S.J.4
Gouverneur, V.5
Houk, K.N.6
-
57
-
-
0034678033
-
Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery
-
Schreiber, S. L. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery Science 2000, 287, 1964-1969
-
(2000)
Science
, vol.287
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
58
-
-
0344515366
-
Diversity-Oriented Synthesis; A Challenge for Synthetic Chemists
-
Spring, D. R. Diversity-Oriented Synthesis; A Challenge for Synthetic Chemists Org. Biomol. Chem. 2003, 1, 3867-3870
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 3867-3870
-
-
Spring, D.R.1
-
59
-
-
3042799070
-
A Planning Strategy for Diversity-Oriented Synthesis
-
Burke, M. D.; Schreiber, S. L. A Planning Strategy for Diversity-Oriented Synthesis Angew. Chem., Int. Ed. 2004, 43, 46-58
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 46-58
-
-
Burke, M.D.1
Schreiber, S.L.2
-
60
-
-
33644839988
-
Diversity-Oriented Synthesis: Exploring the Intersections between Chemistry and Biology
-
Tan, D. S. Diversity-Oriented Synthesis: Exploring the Intersections between Chemistry and Biology Nature Chem. Biol. 2005, 1, 74-84
-
(2005)
Nature Chem. Biol.
, vol.1
, pp. 74-84
-
-
Tan, D.S.1
-
61
-
-
45149134173
-
Diversity Oriented Synthesis of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis-Hillman Reaction and RCM Protocol
-
Radha Krishna, P.; Srinivas Reddy, P. Diversity Oriented Synthesis of Functionalized Chiral Tetrahydropyridines: Potential GABA Receptor Agonists and Azasugars from Natural Amino Acids via a Sequential Baylis-Hillman Reaction and RCM Protocol J. Comb. Chem. 2008, 10, 426-435
-
(2008)
J. Comb. Chem.
, vol.10
, pp. 426-435
-
-
Radha Krishna, P.1
Srinivas Reddy, P.2
-
62
-
-
84862008385
-
Diversity-Oriented Synthesis: Producing Chemical Tools for Dissecting Biology
-
O'Connor, C. J.; Beckmann, H. S. G.; Spring, D. R. Diversity-Oriented Synthesis: Producing Chemical Tools for Dissecting Biology Chem. Soc. Rev. 2012, 41, 4444-4456
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 4444-4456
-
-
O'Connor, C.J.1
Beckmann, H.S.G.2
Spring, D.R.3
-
63
-
-
84911874556
-
-
Ed. John-Wiley & Sons, Inc. Hoboken, New Jersey, USA.
-
Diversity-Oriented Synthesis: Basics and Applications in Organic Synthesis, Drug Discovery and Chemical Biology; Trabocchi, A., Ed.; John-Wiley & Sons, Inc., Hoboken, New Jersey, USA, 2013.
-
(2013)
Diversity-Oriented Synthesis: Basics and Applications in Organic Synthesis, Drug Discovery and Chemical Biology
-
-
Trabocchi, A.1
-
65
-
-
1442360753
-
-
Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany
-
Grubbs, R. H. Handbook of Metathesis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2003; Vol. 1-3.
-
(2003)
Handbook of Metathesis
, vol.13
-
-
Grubbs, R.H.1
-
66
-
-
79955856768
-
-
Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, Vol.
-
Grubbs, R. H.; Schrock, R. R.; Fürstner, A. Advanced Synthesis & Catalysis, Olefin Metathesis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2007, Vol. 349, pp 1-265.
-
(2007)
Advanced Synthesis & Catalysis, Olefin Metathesis
, vol.349
, pp. 1-265
-
-
Grubbs, R.H.1
Schrock, R.R.2
Fürstner, A.3
-
67
-
-
36549001142
-
Synthesis of Diverse Polycyclic Compounds via Catalytic Metathesis
-
Kotha, S.; Lahiri, K. Synthesis of Diverse Polycyclic Compounds via Catalytic Metathesis Synlett 2007, 2767-2784
-
(2007)
Synlett
, pp. 2767-2784
-
-
Kotha, S.1
Lahiri, K.2
-
68
-
-
3343012187
-
Olefin Metathesis
-
Grubbs, R. H. Olefin Metathesis Tetrahedron 2004, 60, 7117-7140
-
(2004)
Tetrahedron
, vol.60
, pp. 7117-7140
-
-
Grubbs, R.H.1
-
69
-
-
0344006321
-
Olefin Metathesis and beyond
-
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
-
70
-
-
36049015757
-
The Remarkable Metal-Catalysed Olefin Metathesis Reaction
-
Hoveyda, A. H.; Zhugralin, A. R. The Remarkable Metal-Catalysed Olefin Metathesis Reaction Nature 2007, 450, 243-251
-
(2007)
Nature
, vol.450
, pp. 243-251
-
-
Hoveyda, A.H.1
Zhugralin, A.R.2
-
71
-
-
0034799755
-
Catalytic Metathesis Reaction in Organic Synthesis
-
Kotha, S.; Sreenivasachary, N. Catalytic Metathesis Reaction in Organic Synthesis Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2001, 40B, 763-780
-
(2001)
Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem.
, vol.40
, pp. 763-780
-
-
Kotha, S.1
Sreenivasachary, N.2
-
72
-
-
82955187545
-
Strategies and Tactics in Olefin Metathesis
-
Kotha, S.; Dipak, M. K. Strategies and Tactics in Olefin Metathesis Tetrahedron 2012, 68, 397-421
-
(2012)
Tetrahedron
, vol.68
, pp. 397-421
-
-
Kotha, S.1
Dipak, M.K.2
-
73
-
-
84873158280
-
Application of Cross Metathesis in Diene and Polyene Synthesis
-
Wojtkielewicz, A. Application of Cross Metathesis in Diene and Polyene Synthesis Curr. Org. Synth. 2013, 10, 43-66
-
(2013)
Curr. Org. Synth.
, vol.10
, pp. 43-66
-
-
Wojtkielewicz, A.1
-
75
-
-
84858392228
-
Rongalite: A Useful Green Reagent in Organic Synthesis
-
Kotha, S.; Khedkar, P. Rongalite: A Useful Green Reagent in Organic Synthesis Chem. Rev. 2012, 112, 1650-1680
-
(2012)
Chem. Rev.
, vol.112
, pp. 1650-1680
-
-
Kotha, S.1
Khedkar, P.2
-
76
-
-
84949117561
-
Diversity-Oriented Approach to Unusual Amino Acid Derivatives and Heterocycles via Methyl 2-Acetamidoacrylate and its Congeners
-
Kotha, S.; Bandarugattu, V. B.; Krishna, N. G. Diversity-Oriented Approach to Unusual Amino Acid Derivatives and Heterocycles via Methyl 2-Acetamidoacrylate and its Congeners Tetrahedron 2014, 70, 5361-5384
-
(2014)
Tetrahedron
, vol.70
, pp. 5361-5384
-
-
Kotha, S.1
Bandarugattu, V.B.2
Krishna, N.G.3
-
77
-
-
0000489613
-
Synthesis of a New Constrained Homoserine
-
Avenoza, A.; Cativiela, C.; Fernández-Recio, M. A.; Peregrina, J. M. Synthesis of a New Constrained Homoserine Synlett 1995, 891-892
-
(1995)
Synlett
, pp. 891-892
-
-
Avenoza, A.1
Cativiela, C.2
Fernández-Recio, M.A.3
Peregrina, J.M.4
-
78
-
-
68949195835
-
Advanced Approach to Polycyclics by a Synergistic Combination of Enyne Metathesis and Diels-Alder Reaction
-
Kotha, S.; Meshram, M.; Tiwari, A. Advanced Approach to Polycyclics by a Synergistic Combination of Enyne Metathesis and Diels-Alder Reaction Chem. Soc. Rev. 2009, 38, 2065-2092
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 2065-2092
-
-
Kotha, S.1
Meshram, M.2
Tiwari, A.3
-
79
-
-
53849135518
-
Benzannulation
-
Kotha, S.; Misra, S.; Halder, S. Benzannulation Tetrahedron 2008, 64, 10775-10790
-
(2008)
Tetrahedron
, vol.64
, pp. 10775-10790
-
-
Kotha, S.1
Misra, S.2
Halder, S.3
-
80
-
-
34250684650
-
Synthesis of Novel Quinone-Amino Acid Hybrids via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps
-
Kotha, S.; Mandal, K.; Banerjee, S.; Mobin, S. M. Synthesis of Novel Quinone-Amino Acid Hybrids via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2007, 1244-1255
-
(2007)
Eur. J. Org. Chem.
, pp. 1244-1255
-
-
Kotha, S.1
Mandal, K.2
Banerjee, S.3
Mobin, S.M.4
-
81
-
-
76349107118
-
Ethyl Isocyanoacetate as a Useful Glycine Equivalent
-
Kotha, S.; Halder, S. Ethyl Isocyanoacetate as a Useful Glycine Equivalent Synlett 2010, 337-354
-
(2010)
Synlett
, pp. 337-354
-
-
Kotha, S.1
Halder, S.2
-
82
-
-
0030785271
-
Synthesis of Conformationally Constrained α-Amino Acid Derivatives Using Ethyl Isocyanoacetate as Glycine Equivalent
-
Kotha, S.; Brahmachary, E. Synthesis of Conformationally Constrained α-Amino Acid Derivatives Using Ethyl Isocyanoacetate as Glycine Equivalent Bioorg. Med. Chem. Lett. 1997, 7, 2719-2722
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2719-2722
-
-
Kotha, S.1
Brahmachary, E.2
-
83
-
-
0042880949
-
Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis
-
Maruoka, K.; Ooi, T. Enantioselective Amino Acid Synthesis by Chiral Phase-Transfer Catalysis Chem. Rev. 2003, 103, 3013-3028
-
(2003)
Chem. Rev.
, vol.103
, pp. 3013-3028
-
-
Maruoka, K.1
Ooi, T.2
-
84
-
-
4143049107
-
The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
-
O'Donnell, M. J. The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters Acc. Chem. Res. 2004, 37, 506-517
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 506-517
-
-
O'Donnell, M.J.1
-
85
-
-
34447272888
-
Recent Advances in Asymmetric Phase-Transfer Catalysis
-
Ooi, T.; Maruoka, K. Recent Advances in Asymmetric Phase-Transfer Catalysis Angew. Chem., Int. Ed. 2007, 46, 4222-4266
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 4222-4266
-
-
Ooi, T.1
Maruoka, K.2
-
86
-
-
84876234339
-
Recent Developments in Asymmetric Phase-Transfer Reactions
-
Shirakawa, S.; Maruoka, K. Recent Developments in Asymmetric Phase-Transfer Reactions Angew. Chem., Int. Ed. 2013, 52, 4312-4348
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 4312-4348
-
-
Shirakawa, S.1
Maruoka, K.2
-
87
-
-
84891042286
-
Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis
-
Maruoka, K. Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany.
-
Ooi, T. Cinchona-Derived Chiral Phase-Transfer Catalysts for Amino Acid Synthesis. In Asymmetric Phase-Transfer Catalysis; Maruoka, K., Ed.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2008.
-
(2008)
Asymmetric Phase-Transfer Catalysis
-
-
Ooi, T.1
-
88
-
-
53649106024
-
Synthesis of a Naturally Occurring Diene-Containing Amino Acid and Its Glutamyl Dipeptide via N -Acyliminium Ion Chemistry
-
Berkheij, M.; Dijkink, J.; David, O. R. P.; Sonke, T.; IJzendoorn, D. R.; Blaauw, R. H.; van Maarseveen, J. H.; Schoemaker, H. E.; Hiemstra, H. Synthesis of a Naturally Occurring Diene-Containing Amino Acid and Its Glutamyl Dipeptide via N -Acyliminium Ion Chemistry Eur. J. Org. Chem. 2008, 914-924
-
(2008)
Eur. J. Org. Chem.
, pp. 914-924
-
-
Berkheij, M.1
Dijkink, J.2
David, O.R.P.3
Sonke, T.4
Ijzendoorn, D.R.5
Blaauw, R.H.6
Van Maarseveen, J.H.7
Schoemaker, H.E.8
Hiemstra, H.9
-
89
-
-
33947508615
-
A Facile Synthesis of Ethyl 2-Acetamido-4-methylenehex-5-enoate, a Versatile Diels-Alder Synthon for the Parallel Synthesis of Novel α-Amino Acid Derivatives
-
Chen, R.; Lee, V.; Adlington, R. M.; Baldwin, J. E. A Facile Synthesis of Ethyl 2-Acetamido-4-methylenehex-5-enoate, a Versatile Diels-Alder Synthon for the Parallel Synthesis of Novel α-Amino Acid Derivatives Synthesis 2007, 113-117
-
(2007)
Synthesis
, pp. 113-117
-
-
Chen, R.1
Lee, V.2
Adlington, R.M.3
Baldwin, J.E.4
-
90
-
-
84859011942
-
Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels-Alder Reaction as Key Steps
-
Kotha, S.; Goyal, D.; Thota, N.; Srinivas, V. Synthesis of Modified Phenylalanine Peptides by Cross Enyne Metathesis and a Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2012, 1843-1850
-
(2012)
Eur. J. Org. Chem.
, pp. 1843-1850
-
-
Kotha, S.1
Goyal, D.2
Thota, N.3
Srinivas, V.4
-
91
-
-
0034124909
-
Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction
-
Kotha, S.; Halder, S.; Brahmachary, E.; Ganesh, T. Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction Synlett 2000, 853-855
-
(2000)
Synlett
, pp. 853-855
-
-
Kotha, S.1
Halder, S.2
Brahmachary, E.3
Ganesh, T.4
-
92
-
-
0037020810
-
Synthesis of Highly Functionalized Phenylalanine Derivatives via Cross-Enyne Metathesis Reactions
-
Kotha, S.; Halder, S.; Brahmachary, E. Synthesis of Highly Functionalized Phenylalanine Derivatives via Cross-Enyne Metathesis Reactions Tetrahedron 2002, 58, 9203-9208
-
(2002)
Tetrahedron
, vol.58
, pp. 9203-9208
-
-
Kotha, S.1
Halder, S.2
Brahmachary, E.3
-
93
-
-
84923275687
-
Diversity Oriented Approach to Phenylalanine Derivatives via the Diels-Alder Reaction Involving Sulfolene Intermediates
-
Kotha, S.; Vijayalaxmi, B. Diversity Oriented Approach to Phenylalanine Derivatives via the Diels-Alder Reaction Involving Sulfolene Intermediates Heterocycles 2015, 90, 226-237
-
(2015)
Heterocycles
, vol.90
, pp. 226-237
-
-
Kotha, S.1
Vijayalaxmi, B.2
-
94
-
-
33750717840
-
Total Synthesis and Biological Evaluation of Viscolin, A 1,3-Diphenylpropane as a Novel Potent Anti-Inflammatory Agent
-
Su, C.-R.; Shen, Y.-C.; Kuo, P.-C.; Leu, Y.-L.; Damu, A. G.; Wang, Y.-H.; Wu, T.-S. Total Synthesis and Biological Evaluation of Viscolin, A 1,3-Diphenylpropane as a Novel Potent Anti-Inflammatory Agent Bioorg. Med. Chem. Lett. 2006, 16, 6155-6160
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 6155-6160
-
-
Su, C.-R.1
Shen, Y.-C.2
Kuo, P.-C.3
Leu, Y.-L.4
Damu, A.G.5
Wang, Y.-H.6
Wu, T.-S.7
-
95
-
-
33749049578
-
Viscolin, a New Chalcone from Viscum Coloratum, Inhibits Human Neutrophil Superoxide Anion and Elastase Release via a Camp-Dependent Pathway
-
Hwang, T.-L.; Leu, Y.-L.; Kao, S.-H.; Tang, M.-C.; Chang, H.-L. Viscolin, a New Chalcone from Viscum Coloratum, Inhibits Human Neutrophil Superoxide Anion and Elastase Release via a Camp-Dependent Pathway Free Radical Biol. Med. 2006, 41, 1433-1441
-
(2006)
Free Radical Biol. Med.
, vol.41
, pp. 1433-1441
-
-
Hwang, T.-L.1
Leu, Y.-L.2
Kao, S.-H.3
Tang, M.-C.4
Chang, H.-L.5
-
96
-
-
0141538154
-
Some 1,2-Diphenylethane Derivatives as Inhibitors of Retinoic Acid-Metabolising Enzymes
-
Greer, V. P.; Mason, P.; Kirby, A. J.; Smith, H. J.; Nicholls, P. J.; Simons, C. Some 1,2-Diphenylethane Derivatives as Inhibitors of Retinoic Acid-Metabolising Enzymes J. Enzyme Inhib. Med. Chem. 2003, 18, 431-443
-
(2003)
J. Enzyme Inhib. Med. Chem.
, vol.18
, pp. 431-443
-
-
Greer, V.P.1
Mason, P.2
Kirby, A.J.3
Smith, H.J.4
Nicholls, P.J.5
Simons, C.6
-
97
-
-
60849130694
-
A Diversity-Oriented Approach to Diphenylalkanes by Strategic Utilization of [2 + 2 + 2] Cyclotrimerization, Cross-Enyne Metathesis and Diels-Alder Reaction
-
Kotha, S.; Khedkar, P. A Diversity-Oriented Approach to Diphenylalkanes by Strategic Utilization of [2 + 2 + 2] Cyclotrimerization, Cross-Enyne Metathesis and Diels-Alder Reaction Eur. J. Org. Chem. 2009, 730-738
-
(2009)
Eur. J. Org. Chem.
, pp. 730-738
-
-
Kotha, S.1
Khedkar, P.2
-
98
-
-
77953518547
-
Design and Synthesis of Benzosultine-sulfone as an o -Xylylene Precursor via Cross-Enyne Metathesis and Rongalite: Further Expansion to Polycyclics via Regioselective Diels-Alder Reaction
-
Kotha, S.; Chavan, A. S. Design and Synthesis of Benzosultine-sulfone as an o -Xylylene Precursor via Cross-Enyne Metathesis and Rongalite: Further Expansion to Polycyclics via Regioselective Diels-Alder Reaction J. Org. Chem. 2010, 75, 4319-4322
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4319-4322
-
-
Kotha, S.1
Chavan, A.S.2
-
99
-
-
80053104330
-
Diversity-Oriented Synthesis of Biaryl Derivatives Using Cross-Enyne Metathesis, Diels-Alder Reaction, and Suzuki-Miyaura Cross-Coupling as Key Steps
-
Kotha, S.; Vittal, S. Diversity-Oriented Synthesis of Biaryl Derivatives Using Cross-Enyne Metathesis, Diels-Alder Reaction, and Suzuki-Miyaura Cross-Coupling as Key Steps Synlett 2011, 2329-2334
-
(2011)
Synlett
, pp. 2329-2334
-
-
Kotha, S.1
Vittal, S.2
-
100
-
-
84924908908
-
Diversity-Oriented Approach to Polycyclics via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps
-
Kotha, S.; Vittal, S.; Banerjee, S.; Dipak, M. K. Diversity-Oriented Approach to Polycyclics via Cross-Enyne Metathesis and Diels-Alder Reaction as Key Steps J. Chem. Sci. 2015, 127, 155-162
-
(2015)
J. Chem. Sci.
, vol.127
, pp. 155-162
-
-
Kotha, S.1
Vittal, S.2
Banerjee, S.3
Dipak, M.K.4
-
101
-
-
0037175592
-
Recent Applications of the Suzuki-Miyaura Cross-Coupling Reaction in Organic Synthesis
-
Kotha, S.; Lahiri, K.; Kashinath, D. Recent Applications of the Suzuki-Miyaura Cross-Coupling Reaction in Organic Synthesis Tetrahedron 2002, 58, 9633-9695
-
(2002)
Tetrahedron
, vol.58
, pp. 9633-9695
-
-
Kotha, S.1
Lahiri, K.2
Kashinath, D.3
-
102
-
-
34250614404
-
Expanding the Diversity of Polycyclic Aromatics through a Suzuki-Miyaura Cross-Coupling Strategy
-
Kotha, S.; Lahiri, K. Expanding the Diversity of Polycyclic Aromatics through a Suzuki-Miyaura Cross-Coupling Strategy Eur. J. Org. Chem. 2007, 1221-1236
-
(2007)
Eur. J. Org. Chem.
, pp. 1221-1236
-
-
Kotha, S.1
Lahiri, K.2
-
103
-
-
62749140780
-
A Retrospective on the Design and Synthesis of Novel Molecules Through a Strategic Consideration of Metathesis and Suzuki-Miyaura Cross-Coupling
-
Kotha, S.; Mandal, K. A Retrospective on the Design and Synthesis of Novel Molecules Through a Strategic Consideration of Metathesis and Suzuki-Miyaura Cross-Coupling Chem. - Asian J. 2009, 4, 354-362
-
(2009)
Chem. - Asian J.
, vol.4
, pp. 354-362
-
-
Kotha, S.1
Mandal, K.2
-
104
-
-
34548746810
-
Metathesis of a Novel Dienediyne System: A Unique Example Involving the Usage of in Situ Generated Ethylene as Cross-Enyne Metathesis Partner
-
Kotha, S.; Mandal, K. Metathesis of a Novel Dienediyne System: A Unique Example Involving the Usage of In Situ Generated Ethylene as Cross-Enyne Metathesis Partner J. Organomet. Chem. 2007, 692, 4921-4927
-
(2007)
J. Organomet. Chem.
, vol.692
, pp. 4921-4927
-
-
Kotha, S.1
Mandal, K.2
-
105
-
-
0037059439
-
Syntheses of Anolignans A and B Using Ruthenium-Catalyzed Cross-Enyne Metathesis
-
Mori, M.; Tonogaki, K.; Nishiguchi, N. Syntheses of Anolignans A and B Using Ruthenium-Catalyzed Cross-Enyne Metathesis J. Org. Chem. 2002, 67, 224-226
-
(2002)
J. Org. Chem.
, vol.67
, pp. 224-226
-
-
Mori, M.1
Tonogaki, K.2
Nishiguchi, N.3
-
106
-
-
0028103876
-
New Lignans from Anogeissus Acuminata with HIV-1 Reverse Transcriptase Inhibitory Activity
-
Rimando, A. M.; Pezzuto, J. M.; Farnsworth, N. R. New Lignans from Anogeissus Acuminata with HIV-1 Reverse Transcriptase Inhibitory Activity J. Nat. Prod. 1994, 57, 896-904
-
(1994)
J. Nat. Prod.
, vol.57
, pp. 896-904
-
-
Rimando, A.M.1
Pezzuto, J.M.2
Farnsworth, N.R.3
-
107
-
-
33947604111
-
A New Versatile Strategy for C-Aryl Glycosides
-
Kaliappan, K. P.; Subrahmanyam, A. V. A New Versatile Strategy for C-Aryl Glycosides Org. Lett. 2007, 9, 1121-1124
-
(2007)
Org. Lett.
, vol.9
, pp. 1121-1124
-
-
Kaliappan, K.P.1
Subrahmanyam, A.V.2
-
108
-
-
77954842290
-
Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C -Aryl Glycosides and Spiro- C -Aryl Glycosides
-
Subrahmanyam, A. V.; Palanichamy, K.; Kaliappan, K. P. Application of an Enyne Metathesis/Diels-Alder Cycloaddition Sequence: A New Versatile Approach to the Syntheses of C -Aryl Glycosides and Spiro- C -Aryl Glycosides Chem. - Eur. J. 2010, 16, 8545-8556
-
(2010)
Chem. - Eur. J.
, vol.16
, pp. 8545-8556
-
-
Subrahmanyam, A.V.1
Palanichamy, K.2
Kaliappan, K.P.3
-
109
-
-
54249086260
-
A Rapid Access to New Fluorinated 1,3-Dienes and Benzylic Fluorides via Metathesis on Propargylic Fluorides
-
Pujari, S. A.; Kaliappan, K. P.; Valleix, A.; Grée, D.; Grée, R. A Rapid Access to New Fluorinated 1,3-Dienes and Benzylic Fluorides via Metathesis on Propargylic Fluorides Synlett 2008, 2503-2507
-
(2008)
Synlett
, pp. 2503-2507
-
-
Pujari, S.A.1
Kaliappan, K.P.2
Valleix, A.3
Grée, D.4
Grée, R.5
-
110
-
-
84890533634
-
One-Pot Cross-Enyne Metathesis (CEYM)/Diels-Alder Reaction of Gem-Difluoropropargylic Alkynes
-
Fustero, S.; Bello, P.; Miró, J.; Sánchez-Roselló, M.; Haufe, G.; del Pozo, C. One-Pot Cross-Enyne Metathesis (CEYM)/Diels-Alder Reaction of Gem-Difluoropropargylic Alkynes Beilstein J. Org. Chem. 2013, 9, 2688-2695
-
(2013)
Beilstein J. Org. Chem.
, vol.9
, pp. 2688-2695
-
-
Fustero, S.1
Bello, P.2
Miró, J.3
Sánchez-Roselló, M.4
Haufe, G.5
Del Pozo, C.6
-
111
-
-
84865201967
-
1,7-Octadiene-Assisted Tandem Multicomponent Cross-Enyne Metathesis (CEYM)/Diels-Alder Reactions: A Useful Alternative to Mori's Conditions
-
Fustero, S.; Bello, P.; Miró, J.; Simón, A.; del Pozo, C. 1,7-Octadiene-Assisted Tandem Multicomponent Cross-Enyne Metathesis (CEYM)/Diels-Alder Reactions: A Useful Alternative to Mori's Conditions Chem. - Eur. J. 2012, 18, 10991-10997
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 10991-10997
-
-
Fustero, S.1
Bello, P.2
Miró, J.3
Simón, A.4
Del Pozo, C.5
-
112
-
-
84880388408
-
A Ruthenium-Based Catalytic System with Switchable Selectivity between Cyclotrimerization and Enyne Metathesis/Diels-Alder Reactions of Terminal Alkynes
-
Karabulut, S.; Sariaslan, B.; Öztürk, B. Ö. A Ruthenium-Based Catalytic System with Switchable Selectivity Between Cyclotrimerization and Enyne Metathesis/Diels-Alder Reactions of Terminal Alkynes Catal. Commun. 2013, 41, 12-16
-
(2013)
Catal. Commun.
, vol.41
, pp. 12-16
-
-
Karabulut, S.1
Sariaslan, B.2
Öztürk, B.O.3
-
113
-
-
0022785312
-
Total Synthesis of Anthracyclinone
-
Krohn, K. Total Synthesis of Anthracyclinone Angew. Chem., Int. Ed. Engl. 1986, 25, 790-807
-
(1986)
Angew. Chem., Int. Ed. Engl.
, vol.25
, pp. 790-807
-
-
Krohn, K.1
-
114
-
-
0001331945
-
Discovery and Development of Anthracycline Antitumour Antibiotics
-
Lown, J. W. Discovery and Development of Anthracycline Antitumour Antibiotics Chem. Soc. Rev. 1993, 22, 165-176
-
(1993)
Chem. Soc. Rev.
, vol.22
, pp. 165-176
-
-
Lown, J.W.1
-
115
-
-
0036158328
-
Enantioselective Synthesis of (+)-4-Demethoxy-1,4-dimethyldaunomycinone
-
Kotha, S.; Stoodely, R. J. Enantioselective Synthesis of (+)-4-Demethoxy-1,4-dimethyldaunomycinone Bioorg. Med. Chem. 2002, 10, 621-624
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 621-624
-
-
Kotha, S.1
Stoodely, R.J.2
-
116
-
-
78650178911
-
Synthetic Approach to cis - And trans -Decalins via Diels-Alder Reaction and Ring-Closing Metathesis as Key Steps: Further Extension to Dioxapropellane Derivative by Ring-Closing Metathesis
-
Kotha, S.; Chavan, A. S.; Dipak, M. K. Synthetic Approach to cis-and trans -Decalins via Diels-Alder Reaction and Ring-Closing Metathesis as Key Steps: Further Extension to Dioxapropellane Derivative by Ring-Closing Metathesis Tetrahedron 2011, 67, 501-504
-
(2011)
Tetrahedron
, vol.67
, pp. 501-504
-
-
Kotha, S.1
Chavan, A.S.2
Dipak, M.K.3
-
117
-
-
64549135853
-
Benzofurans as Efficient Dienophiles in Normal Electron Demand [4 + 2] Cycloadditions
-
Chopin, N.; Gérard, H.; Chataigner, I.; Piettre, S. R. Benzofurans as Efficient Dienophiles in Normal Electron Demand [4 + 2] Cycloadditions J. Org. Chem. 2009, 74, 1237-1246
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1237-1246
-
-
Chopin, N.1
Gérard, H.2
Chataigner, I.3
Piettre, S.R.4
-
118
-
-
78650178039
-
Synthesis of (E)-1-Benzyloxy-3-fluoro-1,3-butadiene: A Novel Fluorinated Diene for Diels-Alder Reactions
-
Hayashi, T.; Usuki, Y.; Wakamatsu, Y.; Iio, H. Synthesis of (E)-1-Benzyloxy-3-fluoro-1,3-butadiene: A Novel Fluorinated Diene for Diels-Alder Reactions Synlett 2010, 2843-2846
-
(2010)
Synlett
, pp. 2843-2846
-
-
Hayashi, T.1
Usuki, Y.2
Wakamatsu, Y.3
Iio, H.4
-
119
-
-
84879307969
-
Two Approaches to the Aromatic Core of the Aminonaphthoquinone Antibiotics
-
Nawrat, C. C.; Palmer, L. I.; Blake, A. J.; Moody, C. J. Two Approaches to the Aromatic Core of the Aminonaphthoquinone Antibiotics J. Org. Chem. 2013, 78, 5587-5603
-
(2013)
J. Org. Chem.
, vol.78
, pp. 5587-5603
-
-
Nawrat, C.C.1
Palmer, L.I.2
Blake, A.J.3
Moody, C.J.4
-
120
-
-
0000123574
-
Preparation and Diels-Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes
-
Kozmin, S. A.; Rawal, V. H. Preparation and Diels-Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes J. Org. Chem. 1997, 62, 5252-5253
-
(1997)
J. Org. Chem.
, vol.62
, pp. 5252-5253
-
-
Kozmin, S.A.1
Rawal, V.H.2
-
121
-
-
0030871612
-
Asymmetric Diels-Alder Reactions of Chiral 1-Amino-3-siloxy-1,3-butadiene: Application to the Enantioselective Synthesis of (-)-α-Elemene
-
Kozmin, S. A.; Rawal, V. H. Asymmetric Diels-Alder Reactions of Chiral 1-Amino-3-siloxy-1,3-butadiene: Application to the Enantioselective Synthesis of (-)-α-Elemene J. Am. Chem. Soc. 1997, 119, 7165-7166
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 7165-7166
-
-
Kozmin, S.A.1
Rawal, V.H.2
-
122
-
-
0034649721
-
A Formal Total Synthesis of Dysidiolide
-
Paczkowski, R.; Maichle-Mössmer, C.; Maier, M. E. A Formal Total Synthesis of Dysidiolide Org. Lett. 2000, 2, 3967-3969
-
(2000)
Org. Lett.
, vol.2
, pp. 3967-3969
-
-
Paczkowski, R.1
Maichle-Mössmer, C.2
Maier, M.E.3
-
123
-
-
0036570864
-
An Efficient Approach to Aspidosperma Alkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes: Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (-)-Quebrachamine
-
Kozmin, S. A.; Iwama, T.; Huang, Y.; Rawal, V. H. An Efficient Approach to Aspidosperma Alkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes: Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (-)-Quebrachamine J. Am. Chem. Soc. 2002, 124, 4628-4641
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 4628-4641
-
-
Kozmin, S.A.1
Iwama, T.2
Huang, Y.3
Rawal, V.H.4
-
124
-
-
70349131589
-
Practical Synthesis and Highly Diastereoselective Diels-Alder Reactions of 1-Alkylthio-3-silyloxybutadienes
-
Holmes, J. M.; Albert, A. L.; Gravel, M. Practical Synthesis and Highly Diastereoselective Diels-Alder Reactions of 1-Alkylthio-3-silyloxybutadienes J. Org. Chem. 2009, 74, 6406-6409
-
(2009)
J. Org. Chem.
, vol.74
, pp. 6406-6409
-
-
Holmes, J.M.1
Albert, A.L.2
Gravel, M.3
-
125
-
-
0038053109
-
Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels-Alder Reactions
-
Hilt, G.; Smolko, K. I. Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels-Alder Reactions Angew. Chem., Int. Ed. 2003, 42, 2795-2797
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 2795-2797
-
-
Hilt, G.1
Smolko, K.I.2
-
126
-
-
20744433957
-
Dihydroaromatic Boronic Esters as Building Blocks for the Synthesis of Phenanthrenes and Phenanthridines
-
Hilt, G.; Hess, W.; Schmidt, F. Dihydroaromatic Boronic Esters as Building Blocks for the Synthesis of Phenanthrenes and Phenanthridines Eur. J. Org. Chem. 2005, 2526-2533
-
(2005)
Eur. J. Org. Chem.
, pp. 2526-2533
-
-
Hilt, G.1
Hess, W.2
Schmidt, F.3
-
127
-
-
84929210484
-
Diels-Alder Reactions
-
Tanaka, K. John-Wiley & Sons, Inc. Hoboken, New Jersey, USA.
-
Hilt, G.; Pünner, F. Diels-Alder Reactions. In Transition Metal-Mediated Aromatic Ring Construction; Tanaka, K., Ed.; John-Wiley & Sons, Inc.: Hoboken, New Jersey, USA, 2013.
-
(2013)
Transition Metal-Mediated Aromatic Ring Construction
-
-
Hilt, G.1
Pünner, F.2
-
128
-
-
62149106948
-
Regiocontrolled Cobalt-Catalyzed Diels-Alder Reactions of Silicon-Functionalized, Terminal, and Internal Alkynes
-
Hilt, G.; Janikowski, J. Regiocontrolled Cobalt-Catalyzed Diels-Alder Reactions of Silicon-Functionalized, Terminal, and Internal Alkynes Org. Lett. 2009, 11, 773-776
-
(2009)
Org. Lett.
, vol.11
, pp. 773-776
-
-
Hilt, G.1
Janikowski, J.2
-
129
-
-
79951836111
-
Regiodiverse Three-Component Synthesis of Arenes
-
Danz, M.; Hilt, G. Regiodiverse Three-Component Synthesis of Arenes Adv. Synth. Catal. 2011, 353, 303-308
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 303-308
-
-
Danz, M.1
Hilt, G.2
-
130
-
-
84859853689
-
Straightforward Synthesis of Nonconjugated Cyclohex-3-enone and Conjugated 4-Methylenecyclohex-2-enone Derivatives
-
Kuttner, J.-R.; Warratz, S.; Hilt, G. Straightforward Synthesis of Nonconjugated Cyclohex-3-enone and Conjugated 4-Methylenecyclohex-2-enone Derivatives Synthesis 2012, 1293-1303
-
(2012)
Synthesis
, pp. 1293-1303
-
-
Kuttner, J.-R.1
Warratz, S.2
Hilt, G.3
-
131
-
-
84862102114
-
Diels-Alder Reactions for the Construction of Cyclopropylarenes
-
Arndt, M.; Hilt, G.; Khlebnikov, A. F.; Kozhushkov, S. I.; de Meijere, A. Diels-Alder Reactions for the Construction of Cyclopropylarenes Eur. J. Org. Chem. 2012, 3112-3121
-
(2012)
Eur. J. Org. Chem.
, pp. 3112-3121
-
-
Arndt, M.1
Hilt, G.2
Khlebnikov, A.F.3
Kozhushkov, S.I.4
De Meijere, A.5
-
132
-
-
84884555599
-
Synthesis of Fluorenone and Anthraquinone Derivatives from Aryl- and Aroyl-Substituted Propiolates
-
Pünner, F.; Schieven, J.; Hilt, G. Synthesis of Fluorenone and Anthraquinone Derivatives from Aryl- and Aroyl-Substituted Propiolates Org. Lett. 2013, 15, 4888-4891
-
(2013)
Org. Lett.
, vol.15
, pp. 4888-4891
-
-
Pünner, F.1
Schieven, J.2
Hilt, G.3
-
133
-
-
84878024814
-
A Strategy for the Synthesis of Anthraquinone-Based Aryl- C -glycosides
-
Anand, N.; Upadhyaya, K.; Ajay, A.; Mahar, R.; Shukla, S. K.; Kumar, B.; Tripathi, R. P. A Strategy for the Synthesis of Anthraquinone-Based Aryl- C -glycosides J. Org. Chem. 2013, 78, 4685-4696
-
(2013)
J. Org. Chem.
, vol.78
, pp. 4685-4696
-
-
Anand, N.1
Upadhyaya, K.2
Ajay, A.3
Mahar, R.4
Shukla, S.K.5
Kumar, B.6
Tripathi, R.P.7
-
134
-
-
0035804403
-
Dendralenes: The Breakthrough
-
Hopf, H. Dendralenes: The Breakthrough Angew. Chem., Int. Ed. 2001, 40, 705-707
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 705-707
-
-
Hopf, H.1
-
135
-
-
67650497848
-
Forgotten Hydrocarbons Prepared
-
Hopf, H. Forgotten Hydrocarbons Prepared Nature 2009, 460, 183-184
-
(2009)
Nature
, vol.460
, pp. 183-184
-
-
Hopf, H.1
-
136
-
-
84857946726
-
Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity
-
Hopf, H.; Sherburn, M. S. Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity Angew. Chem., Int. Ed. 2012, 51, 2298-2338
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 2298-2338
-
-
Hopf, H.1
Sherburn, M.S.2
-
137
-
-
75349102024
-
Practical Synthesis and Reactivity of [3]Dendralene
-
references cited therein.
-
Bradford, T. A.; Payne, A. D.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. Practical Synthesis and Reactivity of [3]Dendralene J. Org. Chem. 2010, 75, 491-494 and references cited therein.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 491-494
-
-
Bradford, T.A.1
Payne, A.D.2
Willis, A.C.3
Paddon-Row, M.N.4
Sherburn, M.S.5
-
138
-
-
0000439081
-
Indium-Mediated γ-Pentadienylation of Aldehydes and Ketones: Cross-Conjugated Trienes for Diene-Transmissive Cycloadditions
-
Woo, S.; Squires, N.; Fallis, A. G. Indium-Mediated γ-Pentadienylation of Aldehydes and Ketones: Cross-Conjugated Trienes for Diene-Transmissive Cycloadditions Org. Lett. 1999, 1, 573-576
-
(1999)
Org. Lett.
, vol.1
, pp. 573-576
-
-
Woo, S.1
Squires, N.2
Fallis, A.G.3
-
139
-
-
0037073206
-
Skeletal Diversity via a Branched Pathway: Efficient Synthesis of 29400 Discrete, Polycyclic Compounds and Their Arraying into Stock Solutions
-
Kwon, O.; Park, S. B.; Schreiber, S. L. Skeletal Diversity via a Branched Pathway: Efficient Synthesis of 29400 Discrete, Polycyclic Compounds and Their Arraying into Stock Solutions J. Am. Chem. Soc. 2002, 124, 13402-13404
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 13402-13404
-
-
Kwon, O.1
Park, S.B.2
Schreiber, S.L.3
-
140
-
-
33744941610
-
A Consecutive Diels-Alder Approach Toward a Tet Repressor Directed Combinatorial Library
-
Kormann, C.; Heinemann, F. W.; Gmeiner, P. A Consecutive Diels-Alder Approach Toward a Tet Repressor Directed Combinatorial Library Tetrahedron 2006, 62, 6899-6908
-
(2006)
Tetrahedron
, vol.62
, pp. 6899-6908
-
-
Kormann, C.1
Heinemann, F.W.2
Gmeiner, P.3
-
141
-
-
80052951954
-
Synthesis of Substituted [3]Dendralenes and Their Unique Cycloaddition Reactions
-
Singh, R.; Ghosh, S. K. Synthesis of Substituted [3]Dendralenes and Their Unique Cycloaddition Reactions Chem. Commun. 2011, 47, 10809-10811
-
(2011)
Chem. Commun.
, vol.47
, pp. 10809-10811
-
-
Singh, R.1
Ghosh, S.K.2
-
142
-
-
79953236981
-
Highly Functionalized, Angularly Anellated Aromatic Compounds from Dendralenes
-
Hopf, H.; Yildizhan, S. Highly Functionalized, Angularly Anellated Aromatic Compounds from Dendralenes Eur. J. Org. Chem. 2011, 2029-2034
-
(2011)
Eur. J. Org. Chem.
, pp. 2029-2034
-
-
Hopf, H.1
Yildizhan, S.2
-
143
-
-
84870663214
-
Synthesis of a Potent Antimalarial Amphilectene
-
Pronin, S. V.; Shenvi, R. A. Synthesis of a Potent Antimalarial Amphilectene J. Am. Chem. Soc. 2012, 134, 19604-19606
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 19604-19606
-
-
Pronin, S.V.1
Shenvi, R.A.2
-
144
-
-
84869159340
-
Nitroso-Dienophile Additions to Dendralenes: A Short Synthesis of Branched Aminosugars
-
Wang, R.; Bojase, G.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. Nitroso-Dienophile Additions to Dendralenes: A Short Synthesis of Branched Aminosugars Org. Lett. 2012, 14, 5652-5655
-
(2012)
Org. Lett.
, vol.14
, pp. 5652-5655
-
-
Wang, R.1
Bojase, G.2
Willis, A.C.3
Paddon-Row, M.N.4
Sherburn, M.S.5
-
145
-
-
84873398391
-
3-Bromopenta-2,4-dienylsilane: A Useful Reagent for the Preparation of [3]Dendralenes and Polycyclic Compounds
-
Rahif, M.; Roux, M.; Thibonnet, J.; Parrain, J.-L. 3-Bromopenta-2,4-dienylsilane: A Useful Reagent for the Preparation of [3]Dendralenes and Polycyclic Compounds Mol. Divers. 2013, 17, 49-53
-
(2013)
Mol. Divers.
, vol.17
, pp. 49-53
-
-
Rahif, M.1
Roux, M.2
Thibonnet, J.3
Parrain, J.-L.4
-
146
-
-
84882242493
-
Domino Cycloaddition Organocascades of Dendralenes
-
Green, N. J.; Lawrence, A. L.; Bojase, G.; Paddon-Row, M. N.; Sherburn, M. S. Domino Cycloaddition Organocascades of Dendralenes Angew. Chem., Int. Ed. 2013, 52, 8333-8336
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 8333-8336
-
-
Green, N.J.1
Lawrence, A.L.2
Bojase, G.3
Paddon-Row, M.N.4
Sherburn, M.S.5
-
147
-
-
0000670716
-
Nouvelle Methode Pour Porter au Maximum la Purete Optique D'un Produit Partiellement Dedouble Sans L'aide D'aucune Substance Chirale
-
Vigneron, J. P.; Dhaenens, M.; Horeau, A. Nouvelle Methode Pour Porter au Maximum la Purete Optique D'un Produit Partiellement Dedouble Sans L'aide D'aucune Substance Chirale Tetrahedron 1973, 29, 1055-1059
-
(1973)
Tetrahedron
, vol.29
, pp. 1055-1059
-
-
Vigneron, J.P.1
Dhaenens, M.2
Horeau, A.3
-
148
-
-
84898077478
-
Furanodendralenes
-
Fallon, T.; Willis, A. C.; Paddon-Row, M. N.; Sherburn, M. S. Furanodendralenes J. Org. Chem. 2014, 79, 3185-3193
-
(2014)
J. Org. Chem.
, vol.79
, pp. 3185-3193
-
-
Fallon, T.1
Willis, A.C.2
Paddon-Row, M.N.3
Sherburn, M.S.4
-
149
-
-
0032482523
-
Synthesis of Constrained α-Amino Acid Derivatives via Diels-Alder Approach
-
Kotha, S.; Brahmachary, E.; Sreenivasachary, N. Synthesis of Constrained α-Amino Acid Derivatives via Diels-Alder Approach Tetrahedron Lett. 1998, 39, 4095-4098
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 4095-4098
-
-
Kotha, S.1
Brahmachary, E.2
Sreenivasachary, N.3
-
150
-
-
0035898249
-
Synthesis of Benzocycloheptene-Based Amino Acid Derivatives via a [4 + 2] Cycloaddition Reaction as a Key Step
-
Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Synthesis of Benzocycloheptene-Based Amino Acid Derivatives via a [4 + 2] Cycloaddition Reaction as a Key Step Tetrahedron 2001, 57, 6261-6265
-
(2001)
Tetrahedron
, vol.57
, pp. 6261-6265
-
-
Kotha, S.1
Sreenivasachary, N.2
Brahmachary, E.3
-
151
-
-
63849267472
-
Selected Synthetic Strategies to Spirocyclics
-
Kotha, S.; Deb, A. C.; Lahiri, K.; Manivannan, E. Selected Synthetic Strategies to Spirocyclics Synthesis 2009, 165-193
-
(2009)
Synthesis
, pp. 165-193
-
-
Kotha, S.1
Deb, A.C.2
Lahiri, K.3
Manivannan, E.4
-
153
-
-
84864074706
-
Diversity Oriented Approach to Crownophanes by Enyne Metathesis and Diels-Alder Reaction as Key Steps
-
Kotha, S.; Waghule, G. T. Diversity Oriented Approach to Crownophanes by Enyne Metathesis and Diels-Alder Reaction as Key Steps J. Org. Chem. 2012, 77, 6314-6318
-
(2012)
J. Org. Chem.
, vol.77
, pp. 6314-6318
-
-
Kotha, S.1
Waghule, G.T.2
-
154
-
-
23744463470
-
Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates
-
Yamamoto, Y.; Hayashi, H.; Saigoku, T.; Nishiyama, H. Domino Coupling Relay Approach to Polycyclic Pyrrole-2-carboxylates J. Am. Chem. Soc. 2005, 127, 10804-10805
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10804-10805
-
-
Yamamoto, Y.1
Hayashi, H.2
Saigoku, T.3
Nishiyama, H.4
-
155
-
-
0000450167
-
O -Quinodimethanes: Efficient Intermediates in Organic Synthesis
-
Segura, J. L.; Martin, N. o -Quinodimethanes: Efficient Intermediates in Organic Synthesis Chem. Rev. 1999, 99, 3199-3246
-
(1999)
Chem. Rev.
, vol.99
, pp. 3199-3246
-
-
Segura, J.L.1
Martin, N.2
-
156
-
-
33744843463
-
Recent Advances in o -Quinodimethane Chemistry
-
Martin, N.; Seoane, C.; Hanack, M. Recent Advances in o -Quinodimethane Chemistry Org. Prep. Proced. Int. 1991, 23, 237-272
-
(1991)
Org. Prep. Proced. Int.
, vol.23
, pp. 237-272
-
-
Martin, N.1
Seoane, C.2
Hanack, M.3
-
158
-
-
85065852858
-
Intramolecular Cycloaddition Reactions of ortho-Quinodimethanes in Organic Synthesis
-
Oppolzer, W. Intramolecular Cycloaddition Reactions of ortho-Quinodimethanes in Organic Synthesis Synthesis 1978, 793-802
-
(1978)
Synthesis
, pp. 793-802
-
-
Oppolzer, W.1
-
159
-
-
3342991480
-
Generation and Cycloaddition of o -Quinodimethane in Aqueous Medium
-
Bieber, L. W.; Da Silva, M. F. Generation and Cycloaddition of o -Quinodimethane in Aqueous Medium Molecules 2001, 6, 472-476
-
(2001)
Molecules
, vol.6
, pp. 472-476
-
-
Bieber, L.W.1
Da Silva, M.F.2
-
160
-
-
33751500734
-
A Convenient Synthesis of 1,4-Dihydro-2,3-Benzoxathiin 3-Oxide, A Useful Precursor of o -Quinodimethane
-
Hoey, M. D.; Dittmer, D. C. A Convenient Synthesis of 1,4-Dihydro-2,3-Benzoxathiin 3-Oxide, A Useful Precursor of o -Quinodimethane J. Org. Chem. 1991, 56, 1947-1948
-
(1991)
J. Org. Chem.
, vol.56
, pp. 1947-1948
-
-
Hoey, M.D.1
Dittmer, D.C.2
-
161
-
-
0034618229
-
Diels-Alder Approach to Tetralin-Based Constrained α-Amino Acid Derivatives
-
Kotha, S.; Ganesh, T.; Ghosh, A. K. Diels-Alder Approach to Tetralin-Based Constrained α-Amino Acid Derivatives Bioorg. Med. Chem. Lett. 2000, 10, 1755-1757
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1755-1757
-
-
Kotha, S.1
Ganesh, T.2
Ghosh, A.K.3
-
162
-
-
1642309197
-
The Diels-Alder Approach for the Synthesis of Tetralin-Based α-Amino Acid Derivatives and their Modification by the Suzuki-Miyaura Cross-Coupling Reaction
-
Kotha, S.; Ghosh, A. K. The Diels-Alder Approach for the Synthesis of Tetralin-Based α-Amino Acid Derivatives and their Modification by the Suzuki-Miyaura Cross-Coupling Reaction Synthesis 2004, 558-567
-
(2004)
Synthesis
, pp. 558-567
-
-
Kotha, S.1
Ghosh, A.K.2
-
163
-
-
84863927924
-
Diversity Oriented Approach to Polycyclic Compounds through the Diels-Alder Reaction and the Suzuki Coupling
-
Kotha, S.; Misra, S.; Srinivas, V. Diversity Oriented Approach to Polycyclic Compounds through the Diels-Alder Reaction and the Suzuki Coupling Eur. J. Org. Chem. 2012, 4052-4062
-
(2012)
Eur. J. Org. Chem.
, pp. 4052-4062
-
-
Kotha, S.1
Misra, S.2
Srinivas, V.3
-
164
-
-
79952758389
-
Synthesis of Polycyclic Aromatics from a Diiodosultine by Suzuki-Miyaura Cross-Coupling and Diels-Alder Reaction
-
Kotha, S.; Meshram, M. Synthesis of Polycyclic Aromatics from a Diiodosultine by Suzuki-Miyaura Cross-Coupling and Diels-Alder Reaction Heterocycles 2011, 82, 1663-1668
-
(2011)
Heterocycles
, vol.82
, pp. 1663-1668
-
-
Kotha, S.1
Meshram, M.2
-
165
-
-
1642399542
-
A Diels-Alder Approach for the Synthesis of Highly Functionalized Benzo-Annulated Indane-Based α-Amino Acid Derivatives via a Sultine Intermediate
-
Kotha, S.; Ghosh, A. K. A Diels-Alder Approach for the Synthesis of Highly Functionalized Benzo-Annulated Indane-Based α-Amino Acid Derivatives via a Sultine Intermediate Tetrahedron Lett. 2004, 45, 2931-2934
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 2931-2934
-
-
Kotha, S.1
Ghosh, A.K.2
-
166
-
-
14344253325
-
Cycloaddition Approach to Benzo-Annulated Indane-Based α-Amino Acid Derivatives
-
Kotha, S.; Ghosh, A. K. Cycloaddition Approach to Benzo-Annulated Indane-Based α-Amino Acid Derivatives Tetrahedron 2004, 60, 10833-10841
-
(2004)
Tetrahedron
, vol.60
, pp. 10833-10841
-
-
Kotha, S.1
Ghosh, A.K.2
-
167
-
-
72449148320
-
Synthesis of Non-Proteinogenic Phenylalanine Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition Reactions
-
Garcia, L.; Pla-Quintana, A.; Roglans, A. Synthesis of Non-Proteinogenic Phenylalanine Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition Reactions Org. Biomol. Chem. 2009, 7, 5020-5027
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 5020-5027
-
-
Garcia, L.1
Pla-Quintana, A.2
Roglans, A.3
-
168
-
-
34848908965
-
Synthesis of Indanones via Solid-Supported [2 + 2 + 2] Cyclotrimerization
-
Senaiar, R. S.; Teske, J. A.; Young, D. D.; Deiters, A. Synthesis of Indanones via Solid-Supported [2 + 2 + 2] Cyclotrimerization J. Org. Chem. 2007, 72, 7801-7804
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7801-7804
-
-
Senaiar, R.S.1
Teske, J.A.2
Young, D.D.3
Deiters, A.4
-
169
-
-
0035013018
-
Fullerene-Based Amino Acids and Peptides
-
Bianco, A.; Da Ros, T.; Prato, M.; Toniolo, C. Fullerene-Based Amino Acids and Peptides J. Pept. Sci. 2001, 7, 208-219
-
(2001)
J. Pept. Sci.
, vol.7
, pp. 208-219
-
-
Bianco, A.1
Da Ros, T.2
Prato, M.3
Toniolo, C.4
-
170
-
-
0033590932
-
Medicinal Chemistry with Fullerenes and Fullerene Derivatives
-
Da Ros, T.; Prato, M. Medicinal Chemistry with Fullerenes and Fullerene Derivatives Chem. Commun. 1999, 663-669
-
(1999)
Chem. Commun.
, pp. 663-669
-
-
Da Ros, T.1
Prato, M.2
-
171
-
-
0037195722
-
Synthesis and Characterization of Mono- and Bis-methano[60]fullerenyl Amino Acid Derivatives and Their Reductive Ring-Opening Retro-Bingel Reactions
-
Burley, G. A.; Keller, P. A.; Pyne, S. G.; Ball, G. E. Synthesis and Characterization of Mono- and Bis-methano[60]fullerenyl Amino Acid Derivatives and Their Reductive Ring-Opening Retro-Bingel Reactions J. Org. Chem. 2002, 67, 8316-8330
-
(2002)
J. Org. Chem.
, vol.67
, pp. 8316-8330
-
-
Burley, G.A.1
Keller, P.A.2
Pyne, S.G.3
Ball, G.E.4
-
172
-
-
34247153415
-
Synthesis of Novel 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid Derivatives Through the Application of Rongalite: A Synergistic Combination of [2 + 2 + 2]- and [4 + 2] Cycloaddition Reactions
-
Kotha, S.; Banerjee, S. Synthesis of Novel 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid Derivatives Through the Application of Rongalite: A Synergistic Combination of [2 + 2 + 2]- and [4 + 2] Cycloaddition Reactions Synthesis 2007, 1015-1020
-
(2007)
Synthesis
, pp. 1015-1020
-
-
Kotha, S.1
Banerjee, S.2
-
173
-
-
0034601143
-
A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid (Tic) Derivatives via a [2 + 2 + 2] Cycloaddition Reaction
-
Kotha, S.; Sreenivasachary, N. A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid (Tic) Derivatives via a [2 + 2 + 2] Cycloaddition Reaction Bioorg. Med. Chem. Lett. 2000, 10, 1413-1415
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1413-1415
-
-
Kotha, S.1
Sreenivasachary, N.2
-
174
-
-
40949129637
-
Ruthenium-Catalyzed Cyclotrimerization of 1,6- and 1,7-Azadiynes: New Access to Fluorinated Bicyclic Amino Acids
-
Shchetnikov, G. T.; Osipov, S. N.; Bruneau, C.; Dixneuf, P. H. Ruthenium-Catalyzed Cyclotrimerization of 1,6- and 1,7-Azadiynes: New Access to Fluorinated Bicyclic Amino Acids Synlett 2008, 578-582
-
(2008)
Synlett
, pp. 578-582
-
-
Shchetnikov, G.T.1
Osipov, S.N.2
Bruneau, C.3
Dixneuf, P.H.4
-
175
-
-
36448995803
-
Synthesis of Crown-Based Sulfones via Rongalite: Diversity-Oriented Approach to Annulated Benzocrowns by Diels-Alder Reactions
-
Kotha, S.; Kashinath, D.; Khedkar, P. Synthesis of Crown-Based Sulfones via Rongalite: Diversity-Oriented Approach to Annulated Benzocrowns by Diels-Alder Reactions Synthesis 2007, 3357-3360
-
(2007)
Synthesis
, pp. 3357-3360
-
-
Kotha, S.1
Kashinath, D.2
Khedkar, P.3
-
176
-
-
0346522068
-
The Synthesis of Naphthosultine and Benzodisultines and Their Pyrolysis with Dienophiles: Studies on o -Naphthoquinodimethane and Bis- o -Quinodimethane
-
Wu, A.-T.; Liu, W.-D.; Chung, W.-S. The Synthesis of Naphthosultine and Benzodisultines and Their Pyrolysis with Dienophiles: Studies on o -Naphthoquinodimethane and Bis- o -Quinodimethane J. Chin. Chem. Soc. 2002, 49, 77-82
-
(2002)
J. Chin. Chem. Soc.
, vol.49
, pp. 77-82
-
-
Wu, A.-T.1
Liu, W.-D.2
Chung, W.-S.3
-
177
-
-
0038558792
-
Condensed Cyclobutane Aromatic Compounds. XI. Benzo[1,2:4,5]dicyclobutene
-
Cava, M. P.; Deana, A. A.; Muth, K. Condensed Cyclobutane Aromatic Compounds. XI. Benzo[1,2:4,5]dicyclobutene J. Am. Chem. Soc. 1960, 82, 2524-2525
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 2524-2525
-
-
Cava, M.P.1
Deana, A.A.2
Muth, K.3
-
178
-
-
0040327344
-
The Repetitive Diels-Alder Reaction: A New Approach to [60]Fullerene Maindashchain Polymers
-
Gügel, A.; Belik, P.; Walter, M.; Kraus, A.; Harth, E.; Wagner, M.; Spickermann, J.; Müllen, K. The Repetitive Diels-Alder Reaction: A New Approach to [60]Fullerene Maindashchain Polymers Tetrahedron 1996, 52, 5007-5014
-
(1996)
Tetrahedron
, vol.52
, pp. 5007-5014
-
-
Gügel, A.1
Belik, P.2
Walter, M.3
Kraus, A.4
Harth, E.5
Wagner, M.6
Spickermann, J.7
Müllen, K.8
-
179
-
-
0035924931
-
Recent Chemistry of Benzocyclobutenes
-
Mehta, G.; Kotha, S. Recent Chemistry of Benzocyclobutenes Tetrahedron 2001, 57, 625-659
-
(2001)
Tetrahedron
, vol.57
, pp. 625-659
-
-
Mehta, G.1
Kotha, S.2
-
180
-
-
68049089944
-
Differential Reactivity Pattern of Hybrid o -Quinodimethane Precursors: Strategic Expansion to Annulated Benzocycloalkanes via Rongalite
-
Kotha, S.; Khedkar, P. Differential Reactivity Pattern of Hybrid o -Quinodimethane Precursors: Strategic Expansion to Annulated Benzocycloalkanes via Rongalite J. Org. Chem. 2009, 74, 5667-5670
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5667-5670
-
-
Kotha, S.1
Khedkar, P.2
-
181
-
-
80755171506
-
Synthetic Approach to Linearly Annulated Tetralin-Based Constrained α-Amino Acid Derivatives via Rongalite
-
Kotha, S.; Krishna, N. G. Synthetic Approach to Linearly Annulated Tetralin-Based Constrained α-Amino Acid Derivatives via Rongalite Curr. Sci. 2011, 101, 923-926
-
(2011)
Curr. Sci.
, vol.101
, pp. 923-926
-
-
Kotha, S.1
Krishna, N.G.2
-
182
-
-
84901643580
-
Synthesis of Novel Fluoranthene-Based Conformationally Constrained α-Amino Acid Derivatives and Polycyclic Aromatics via the Diels-Alder Reaction
-
Kotha, S.; Meshram, M. Synthesis of Novel Fluoranthene-Based Conformationally Constrained α-Amino Acid Derivatives and Polycyclic Aromatics via the Diels-Alder Reaction Synthesis 2014, 1525-1531
-
(2014)
Synthesis
, pp. 1525-1531
-
-
Kotha, S.1
Meshram, M.2
-
183
-
-
84881522076
-
Diversity-Oriented Approach to Novel Spirocyclics via Enyne Metathesis, Diels-Alder Reaction, and a [2 + 2 + 2] Cycloaddition as Key Steps
-
Kotha, S.; Ali, R.; Tiwari, A. Diversity-Oriented Approach to Novel Spirocyclics via Enyne Metathesis, Diels-Alder Reaction, and a [2 + 2 + 2] Cycloaddition as Key Steps Synlett 2013, 1921-1926
-
(2013)
Synlett
, pp. 1921-1926
-
-
Kotha, S.1
Ali, R.2
Tiwari, A.3
-
184
-
-
84923095923
-
Diversity-Oriented Approach to Linearly Fused Spirocycles via Strategic Utilization of a [2 + 2 + 2] Cycloaddition and the Diels-Alder Reaction
-
Kotha, S.; Ali, R. Diversity-Oriented Approach to Linearly Fused Spirocycles via Strategic Utilization of a [2 + 2 + 2] Cycloaddition and the Diels-Alder Reaction Tetrahedron 2015, 71, 1597-1603
-
(2015)
Tetrahedron
, vol.71
, pp. 1597-1603
-
-
Kotha, S.1
Ali, R.2
-
185
-
-
84987616126
-
Diversity Oriented Approach to Spirobarbituric Acid Derivatives via a [2 + 2 + 2] Cycloaddition and Diels-Alder Reaction as Key Steps
-
Kotha, S.; Ali, R. Diversity Oriented Approach to Spirobarbituric Acid Derivatives via a [2 + 2 + 2] Cycloaddition and Diels-Alder Reaction as Key Steps Heterocycles 2014, 88, 789-797
-
(2014)
Heterocycles
, vol.88
, pp. 789-797
-
-
Kotha, S.1
Ali, R.2
-
186
-
-
84923284136
-
Diversity-Oriented Approach to Oxepine Derivatives: Further Expansion via Diels-Alder Reaction
-
Kotha, S.; Ali, R. Diversity-Oriented Approach to Oxepine Derivatives: Further Expansion via Diels-Alder Reaction Heterocycles 2015, 90, 645-658
-
(2015)
Heterocycles
, vol.90
, pp. 645-658
-
-
Kotha, S.1
Ali, R.2
-
187
-
-
0034595627
-
The Syntheses of Pyrazino-Containing Sultines and Their Application in Diels-Alder Reactions with Electron-Poor Olefins and [60]Fullerene
-
Liu, J.-H.; Wu, A.-T.; Huang, M.-H.; Wu, C.-W.; Chung, W.-S. The Syntheses of Pyrazino-Containing Sultines and Their Application in Diels-Alder Reactions with Electron-Poor Olefins and [60]Fullerene J. Org. Chem. 2000, 65, 3395-3403
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3395-3403
-
-
Liu, J.-H.1
Wu, A.-T.2
Huang, M.-H.3
Wu, C.-W.4
Chung, W.-S.5
-
188
-
-
0028791849
-
A Facile Formation of Electroactive Fullerene Adducts from Sultines via a Diels-Alder Reaction
-
Illescas, B.; Martín, N.; Seoane, C.; de la Cruz, P.; Langa, F.; Wudl, F. A Facile Formation of Electroactive Fullerene Adducts from Sultines via a Diels-Alder Reaction Tetrahedron Lett. 1995, 36, 8307-8310
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 8307-8310
-
-
Illescas, B.1
Martín, N.2
Seoane, C.3
De La Cruz, P.4
Langa, F.5
Wudl, F.6
-
189
-
-
0000037595
-
Reaction of C60 with Sultines: Synthesis, Electrochemistry, and Theoretical Calculations of Organofullerene Acceptors
-
Illescas, B. M.; Martín, N.; Seoane, C.; Orti, E.; Viruela, P. M.; Viruela, R.; de la Hoz, A. Reaction of C60 with Sultines: Synthesis, Electrochemistry, and Theoretical Calculations of Organofullerene Acceptors J. Org. Chem. 1997, 62, 7585-7591
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7585-7591
-
-
Illescas, B.M.1
Martín, N.2
Seoane, C.3
Orti, E.4
Viruela, P.M.5
Viruela, R.6
De La Hoz, A.7
-
190
-
-
33845184269
-
Syntheses and Electrochemical Properties of Tetracyano- p -Quinodimethane Derivatives Containing Fused Aromatic Rings
-
Martín, N.; Behnisch, R.; Hanack, M. Syntheses and Electrochemical Properties of Tetracyano- p -Quinodimethane Derivatives Containing Fused Aromatic Rings J. Org. Chem. 1989, 54, 2563-2568
-
(1989)
J. Org. Chem.
, vol.54
, pp. 2563-2568
-
-
Martín, N.1
Behnisch, R.2
Hanack, M.3
-
191
-
-
37049071580
-
N, N ′-Dicyanoquinone Diimines (DCNQIs): Unique Acceptors for Conducting Materials
-
Hünig, S. N, N ′-Dicyanoquinone Diimines (DCNQIs): Unique Acceptors for Conducting Materials J. Mater. Chem. 1995, 5, 1469-1479
-
(1995)
J. Mater. Chem.
, vol.5
, pp. 1469-1479
-
-
Hünig, S.1
-
192
-
-
0003595556
-
-
Nalwa, H. S. John-Wiley & Sons Ltd: New York, USA
-
Martín, N.; Seoane, C. Handbook of Conductive Molecules and Polymers; Nalwa, H. S., Ed.; John-Wiley & Sons Ltd: New York, USA, 1997, Vol. 1.
-
(1997)
Handbook of Conductive Molecules and Polymers
, vol.1
-
-
Martín, N.1
Seoane, C.2
-
193
-
-
33845949270
-
Modular Synthesis of Tetrahydrofluorenones from 5-Alkylidene Meldrum's Acids
-
Fillion, E.; Dumas, A. M.; Hogg, S. A. Modular Synthesis of Tetrahydrofluorenones from 5-Alkylidene Meldrum's Acids J. Org. Chem. 2006, 71, 9899-9902
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9899-9902
-
-
Fillion, E.1
Dumas, A.M.2
Hogg, S.A.3
-
194
-
-
77954736355
-
Facile Access to Boryltetralins and Borylnaphthalenes via a Cycloaddition Using o -Quinodimethanes
-
Yoshida, H.; Mukae, M.; Ohshita, J. Facile Access to Boryltetralins and Borylnaphthalenes via a Cycloaddition Using o -Quinodimethanes Chem. Commun. 2010, 46, 5253-5255
-
(2010)
Chem. Commun.
, vol.46
, pp. 5253-5255
-
-
Yoshida, H.1
Mukae, M.2
Ohshita, J.3
-
195
-
-
0041967557
-
Highly Enantioselective Diels-Alder Reaction of a Photochemically Generated o -Quinodimethane with Olefins
-
Grosch, B.; Orlebar, C. N.; Herdtweck, E.; Massa, W.; Bach, T. Highly Enantioselective Diels-Alder Reaction of a Photochemically Generated o -Quinodimethane with Olefins Angew. Chem., Int. Ed. 2003, 42, 3693-3696
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3693-3696
-
-
Grosch, B.1
Orlebar, C.N.2
Herdtweck, E.3
Massa, W.4
Bach, T.5
-
196
-
-
33745400676
-
Enantioselective Diels-Alder Reaction of o -Quinodimethanes by Utilizing Tartaric Acid Ester as a Chiral Auxiliary
-
Takinami, M.; Ukaji, Y.; Inomata, K. Enantioselective Diels-Alder Reaction of o -Quinodimethanes by Utilizing Tartaric Acid Ester as a Chiral Auxiliary Tetrahedron: Asymmetry 2006, 17, 1554-1560
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 1554-1560
-
-
Takinami, M.1
Ukaji, Y.2
Inomata, K.3
-
197
-
-
34248680992
-
Diastereoselective Cycloaddition of Chiral 1-Acryloyl-2-Imidazolidinone and o -Quinodimethane Generated by Reduction of 1,2-Bis(bromomethyl)benzene with Zinc
-
Kise, N.; Mimura, R. Diastereoselective Cycloaddition of Chiral 1-Acryloyl-2-Imidazolidinone and o -Quinodimethane Generated by Reduction of 1,2-Bis(bromomethyl)benzene with Zinc Tetrahedron: Asymmetry 2007, 18, 988-993
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 988-993
-
-
Kise, N.1
Mimura, R.2
-
198
-
-
80053089739
-
Asymmetric Catalysis of Diels-Alder Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes
-
Liu, Y.; Nappi, M.; Arceo, E.; Vera, S.; Melchiorre, P. Asymmetric Catalysis of Diels-Alder Reactions with in Situ Generated Heterocyclic ortho-Quinodimethanes J. Am. Chem. Soc. 2011, 133, 15212-15218
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 15212-15218
-
-
Liu, Y.1
Nappi, M.2
Arceo, E.3
Vera, S.4
Melchiorre, P.5
-
199
-
-
84863229385
-
Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels-Alder/Benzoin Reaction Sequence
-
Liu, Y.; Nappi, M.; Escudero-Adán, E. C.; Melchiorre, P. Multicatalytic Asymmetric Synthesis of Complex Tetrahydrocarbazoles via a Diels-Alder/Benzoin Reaction Sequence Org. Lett. 2012, 14, 1310-1313
-
(2012)
Org. Lett.
, vol.14
, pp. 1310-1313
-
-
Liu, Y.1
Nappi, M.2
Escudero-Adán, E.C.3
Melchiorre, P.4
-
200
-
-
84870955024
-
Asymmetric Diels-Alder Reaction of 2-Methyl-3-indolylmethanols via in Situ Generation of o -Quinodimethanes
-
Xiao, Y.-C.; Zhou, Q.-Q.; Dong, L.; Liu, T.-Y.; Chen, Y.-C. Asymmetric Diels-Alder Reaction of 2-Methyl-3-indolylmethanols via in Situ Generation of o -Quinodimethanes Org. Lett. 2012, 14, 5940-5943
-
(2012)
Org. Lett.
, vol.14
, pp. 5940-5943
-
-
Xiao, Y.-C.1
Zhou, Q.-Q.2
Dong, L.3
Liu, T.-Y.4
Chen, Y.-C.5
-
201
-
-
0032580467
-
Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction
-
Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction Tetrahedron Lett. 1998, 39, 2805-2808
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2805-2808
-
-
Kotha, S.1
Sreenivasachary, N.2
Brahmachary, E.3
-
202
-
-
0035135210
-
Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels-Alder Reaction
-
Kotha, S.; Sreenivasachary, N.; Brahmachary, E. Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels-Alder Reaction Eur. J. Org. Chem. 2001, 787-792
-
(2001)
Eur. J. Org. Chem.
, pp. 787-792
-
-
Kotha, S.1
Sreenivasachary, N.2
Brahmachary, E.3
-
203
-
-
42449131742
-
The Schöllkopf Chiron and Transition Metal Mediated Reactions, A Powerful Combination for Stereoselective Construction of Cyclic α-Quaternary-α-Amino Acid Derivatives
-
references cited therein
-
Undheim, K. The Schöllkopf Chiron and Transition Metal Mediated Reactions, A Powerful Combination for Stereoselective Construction of Cyclic α-Quaternary-α-Amino Acid Derivatives Amino Acids 2008, 34, 357-402 and references cited therein
-
(2008)
Amino Acids
, vol.34
, pp. 357-402
-
-
Undheim, K.1
-
204
-
-
84908674593
-
Diversity-oriented Synthesis of Medicinally Important 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (Tic) Derivatives and Higher Analogs
-
Kotha, S.; Deodhar, D.; Khedkar, P. Diversity-oriented Synthesis of Medicinally Important 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (Tic) Derivatives and Higher Analogs Org. Biomol. Chem. 2014, 12, 9054-9091
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 9054-9091
-
-
Kotha, S.1
Deodhar, D.2
Khedkar, P.3
-
205
-
-
0035353817
-
Synthetic Approaches to Tetrahydroisoquinoline-3-carboxylic Acid Derivatives
-
Kotha, S.; Sreenivasachary, N. Synthetic Approaches to Tetrahydroisoquinoline-3-carboxylic Acid Derivatives J. Indian Inst. Sci. 2001, 81, 277-286
-
(2001)
J. Indian Inst. Sci.
, vol.81
, pp. 277-286
-
-
Kotha, S.1
Sreenivasachary, N.2
-
206
-
-
0034696697
-
A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via Enyne Metathesis and the Diels-Alder Reaction
-
Kotha, S.; Sreenivasachary, N. A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via Enyne Metathesis and the Diels-Alder Reaction Chem. Commun. 2000, 503-504
-
(2000)
Chem. Commun.
, pp. 503-504
-
-
Kotha, S.1
Sreenivasachary, N.2
-
207
-
-
0034843209
-
Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches
-
Kotha, S.; Sreenivasachary, N. Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches Eur. J. Org. Chem. 2001, 3375-3383
-
(2001)
Eur. J. Org. Chem.
, pp. 3375-3383
-
-
Kotha, S.1
Sreenivasachary, N.2
-
208
-
-
53249094132
-
Synthesis of a Conformationally Constrained Phenylalanine Derivative by a Strategic Combination of Ring-Closing Enyne Metathesis and Diels-Alder Reaction
-
Kotha, S.; Khedkar, P. Synthesis of a Conformationally Constrained Phenylalanine Derivative by a Strategic Combination of Ring-Closing Enyne Metathesis and Diels-Alder Reaction Synthesis 2008, 2925-2928
-
(2008)
Synthesis
, pp. 2925-2928
-
-
Kotha, S.1
Khedkar, P.2
-
209
-
-
79960983511
-
A Synergistic Approach to Polycyclics via a Strategic Utilization of Claisen Rearrangement and Olefin Metathesis
-
Kotha, S.; Krishna, N. G.; Halder, S.; Misra, S. A Synergistic Approach to Polycyclics via a Strategic Utilization of Claisen Rearrangement and Olefin Metathesis Org. Biomol. Chem. 2011, 9, 5597-5624
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5597-5624
-
-
Kotha, S.1
Krishna, N.G.2
Halder, S.3
Misra, S.4
-
210
-
-
33750552076
-
Diversity-Oriented Approach to Biologically Relevant Molecular Frameworks Starting with β-Naphthol and Using the Claisen Rearrangement and Olefin Metathesis as Key Steps
-
Kotha, S.; Mandal, K.; Tiwari, A.; Mobin, S. M. Diversity-Oriented Approach to Biologically Relevant Molecular Frameworks Starting with β-Naphthol and Using the Claisen Rearrangement and Olefin Metathesis as Key Steps Chem. - Eur. J. 2006, 12, 8024-8038
-
(2006)
Chem. - Eur. J.
, vol.12
, pp. 8024-8038
-
-
Kotha, S.1
Mandal, K.2
Tiwari, A.3
Mobin, S.M.4
-
212
-
-
84906946518
-
Design and Synthesis of Angularly Annulated Spirocyclics via Enyne Metathesis and the Diels-Alder Reaction as Key Steps
-
Kotha, S.; Ali, R.; Tiwari, A. Design and Synthesis of Angularly Annulated Spirocyclics via Enyne Metathesis and the Diels-Alder Reaction as Key Steps Synthesis 2014, 2471-2480
-
(2014)
Synthesis
, pp. 2471-2480
-
-
Kotha, S.1
Ali, R.2
Tiwari, A.3
-
213
-
-
84908438740
-
Diversity-Oriented Approach to Carbocycles and Heterocycles through Ring Rearrangement Metathesis, Fischer Indole Cyclization, and Diels-Alder Reaction as Key Steps
-
Kotha, S.; Ravikumar, O. Diversity-Oriented Approach to Carbocycles and Heterocycles through Ring Rearrangement Metathesis, Fischer Indole Cyclization, and Diels-Alder Reaction as Key Steps Eur. J. Org. Chem. 2014, 5582-5590
-
(2014)
Eur. J. Org. Chem.
, pp. 5582-5590
-
-
Kotha, S.1
Ravikumar, O.2
-
214
-
-
84908446920
-
Design and Synthesis of Oxa-bowls via Diels-Alder Reaction and Ring-Rearrangement Metathesis as Key Steps
-
Kotha, S.; Ravikumar, O. Design and Synthesis of Oxa-bowls via Diels-Alder Reaction and Ring-Rearrangement Metathesis as Key Steps Tetrahedron Lett. 2014, 55, 5781-5784
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 5781-5784
-
-
Kotha, S.1
Ravikumar, O.2
-
215
-
-
33747197191
-
Synthesis of Oxepine-, Oxocine- and Azepine-Annulated Carbazole Derivatives by Combined Claisen Rearrangement and Diene/Enyne Metathesis
-
Chattopadhyay, S. K.; Roy, S. P.; Ghosh, D.; Biswas, G. Synthesis of Oxepine-, Oxocine- and Azepine-Annulated Carbazole Derivatives by Combined Claisen Rearrangement and Diene/Enyne Metathesis Tetrahedron Lett. 2006, 47, 6895-6898
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 6895-6898
-
-
Chattopadhyay, S.K.1
Roy, S.P.2
Ghosh, D.3
Biswas, G.4
-
216
-
-
84856733921
-
A New Entry to the Phenanthridine Ring System
-
Mondal, P.; Thander, L.; Chattopadhyay, S. K. A New Entry to the Phenanthridine Ring System Tetrahedron Lett. 2012, 53, 1328-1331
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 1328-1331
-
-
Mondal, P.1
Thander, L.2
Chattopadhyay, S.K.3
-
217
-
-
53649100112
-
Design and Synthesis of 1-Benzazepine Derivatives by Strategic Utilization of Suzuki-Miyaura Cross-Coupling, Aza-Claisen Rearrangement and Ring-Closing Metathesis
-
Kotha, S.; Shah, V. R. Design and Synthesis of 1-Benzazepine Derivatives by Strategic Utilization of Suzuki-Miyaura Cross-Coupling, Aza-Claisen Rearrangement and Ring-Closing Metathesis Eur. J. Org. Chem. 2008, 1054-1064
-
(2008)
Eur. J. Org. Chem.
, pp. 1054-1064
-
-
Kotha, S.1
Shah, V.R.2
-
218
-
-
67651083203
-
Recent Advances in the Aza-Claisen Rearrangement
-
Majumdar, K. C.; Bhattacharyya, T.; Chattopadhyay, B.; Sinha, B. Recent Advances in the Aza-Claisen Rearrangement Synthesis 2009, 2117-2142
-
(2009)
Synthesis
, pp. 2117-2142
-
-
Majumdar, K.C.1
Bhattacharyya, T.2
Chattopadhyay, B.3
Sinha, B.4
-
219
-
-
65649110353
-
Aza-Claisen Rearrangement
-
Hiersemann, M. Nubbemeyer, U. Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany
-
Nubbemeyer, U. Aza-Claisen Rearrangement. In The Claisen Rearrangement: Methods and Applications; Hiersemann, M.; Nubbemeyer, U., Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2007; pp 461-523.
-
(2007)
The Claisen Rearrangement: Methods and Applications
, pp. 461-523
-
-
Nubbemeyer, U.1
-
220
-
-
79960166033
-
Total Synthesis of Isofregenedadiol
-
Kurhade, S. E.; Sanchawala, A. I.; Ravikumar, V.; Bhuniya, D.; Srinivasa Reddy, D. Total Synthesis of Isofregenedadiol Org. Lett. 2011, 13, 3690-3693
-
(2011)
Org. Lett.
, vol.13
, pp. 3690-3693
-
-
Kurhade, S.E.1
Sanchawala, A.I.2
Ravikumar, V.3
Bhuniya, D.4
Srinivasa Reddy, D.5
-
221
-
-
84859239885
-
A Unified Strategy for the Syntheses of Angucyclinone Antibiotics: Total Syntheses of Tetrangulol, Kanglemycin M, X-14881-E, and Anhydrolandomycinone
-
Vanga, D. G.; Kaliappan, K. P. A Unified Strategy for the Syntheses of Angucyclinone Antibiotics: Total Syntheses of Tetrangulol, Kanglemycin M, X-14881-E, and Anhydrolandomycinone Eur. J. Org. Chem. 2012, 2250-2259
-
(2012)
Eur. J. Org. Chem.
, pp. 2250-2259
-
-
Vanga, D.G.1
Kaliappan, K.P.2
-
222
-
-
84868451154
-
Total Synthesis and Stereochemical Assignment of (-)-Zenkequinone B
-
Vanga, D. G.; Kaliappan, K. P. Total Synthesis and Stereochemical Assignment of (-)-Zenkequinone B Synlett 2012, 2931-2934
-
(2012)
Synlett
, pp. 2931-2934
-
-
Vanga, D.G.1
Kaliappan, K.P.2
-
223
-
-
84864069841
-
Discovery of a Multi-Bond Forming, Four-Step Tandem Process: Construction of Drug-Like Polycyclic Scaffolds
-
Grafton, M. W.; Farrugia, L. J.; Senn, H. M.; Sutherland, A. Discovery of a Multi-Bond Forming, Four-Step Tandem Process: Construction of Drug-Like Polycyclic Scaffolds Chem. Commun. 2012, 48, 7994-7996
-
(2012)
Chem. Commun.
, vol.48
, pp. 7994-7996
-
-
Grafton, M.W.1
Farrugia, L.J.2
Senn, H.M.3
Sutherland, A.4
-
224
-
-
0022376894
-
A Stereorational Total Synthesis of (-)-Ptilocaulin
-
Walts, A. E.; Roush, W. R. A Stereorational Total Synthesis of (-)-Ptilocaulin Tetrahedron 1985, 41, 3463-3478
-
(1985)
Tetrahedron
, vol.41
, pp. 3463-3478
-
-
Walts, A.E.1
Roush, W.R.2
-
225
-
-
33845277931
-
Acid-Catalyzed Reactions of Hapalindoles
-
Bonjouklian, R.; Moore, R. E.; Patterson, G. M. L. Acid-Catalyzed Reactions of Hapalindoles J. Org. Chem. 1988, 53, 5866-5870
-
(1988)
J. Org. Chem.
, vol.53
, pp. 5866-5870
-
-
Bonjouklian, R.1
Moore, R.E.2
Patterson, G.M.L.3
-
226
-
-
84880548994
-
Synthesis of Amino-Substituted Indanes and Tetralins via Consecutive Multibond-Forming Tandem Processes
-
Grafton, M. W.; Farrugia, L. J.; Sutherland, A. Synthesis of Amino-Substituted Indanes and Tetralins via Consecutive Multibond-Forming Tandem Processes J. Org. Chem. 2013, 78, 7199-7207
-
(2013)
J. Org. Chem.
, vol.78
, pp. 7199-7207
-
-
Grafton, M.W.1
Farrugia, L.J.2
Sutherland, A.3
-
227
-
-
77954557653
-
Construction of a Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway
-
Oh, S.; Jang, H. J.; Ko, S. K.; Ko, Y.; Park, S. B. Construction of a Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway J. Comb. Chem. 2010, 12, 548-558
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 548-558
-
-
Oh, S.1
Jang, H.J.2
Ko, S.K.3
Ko, Y.4
Park, S.B.5
-
228
-
-
80052779364
-
Versatile Solid-Phase Synthesis of Chromenes Resembling Classical Cannabinoids
-
Kapeller, D. C.; Bräse, S. Versatile Solid-Phase Synthesis of Chromenes Resembling Classical Cannabinoids ACS Comb. Sci. 2011, 13, 554-561
-
(2011)
ACS Comb. Sci.
, vol.13
, pp. 554-561
-
-
Kapeller, D.C.1
Bräse, S.2
-
229
-
-
84863116367
-
Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway: Part II
-
Zhu, M.; Lim, B. J.; Koh, M.; Park, S. B. Construction of Polyheterocyclic Benzopyran Library with Diverse Core Skeletons through Diversity-Oriented Synthesis Pathway: Part II ACS Comb. Sci. 2012, 14, 124-134
-
(2012)
ACS Comb. Sci.
, vol.14
, pp. 124-134
-
-
Zhu, M.1
Lim, B.J.2
Koh, M.3
Park, S.B.4
-
230
-
-
78651247094
-
Diversity Through a Branched Reaction Pathway: Generation of Multicyclic Scaffolds and Identification of Antimigratory Agents
-
Wang, Z.; Castellano, S.; Kinderman, S. S.; Argueta, C. E.; Beshir, A. B.; Fenteany, G.; Kwon, O. Diversity Through a Branched Reaction Pathway: Generation of Multicyclic Scaffolds and Identification of Antimigratory Agents Chem. - Eur. J. 2011, 17, 649-654
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 649-654
-
-
Wang, Z.1
Castellano, S.2
Kinderman, S.S.3
Argueta, C.E.4
Beshir, A.B.5
Fenteany, G.6
Kwon, O.7
-
231
-
-
79955568049
-
Diversity Through Phosphine Catalysis Identifies Octahydro-1,6-naphthyridin-4-ones as Activators of Endothelium-Driven Immunity
-
Cruz, D.; Wang, Z.; Kibbie, J.; Modlin, R.; Kwon, O. Diversity Through Phosphine Catalysis Identifies Octahydro-1,6-naphthyridin-4-ones as Activators of Endothelium-Driven Immunity Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 6769-6774
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 6769-6774
-
-
Cruz, D.1
Wang, Z.2
Kibbie, J.3
Modlin, R.4
Kwon, O.5
-
232
-
-
84865676018
-
A Two-Directional Strategy for the Diversity-Oriented Synthesis of Macrocyclic Scaffolds
-
O'Connell, K. M. G.; Beckmann, H. S. G.; Laraia, L.; Horsley, H. T.; Bender, A.; Venkitaraman, A. R.; Spring, D. R. A Two-Directional Strategy for the Diversity-Oriented Synthesis of Macrocyclic Scaffolds Org. Biomol. Chem. 2012, 10, 7545-7551
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 7545-7551
-
-
O'Connell, K.M.G.1
Beckmann, H.S.G.2
Laraia, L.3
Horsley, H.T.4
Bender, A.5
Venkitaraman, A.R.6
Spring, D.R.7
-
233
-
-
79952448533
-
A Rapid Assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig/Diels-Alder Reaction
-
Torney, P.; Patre, R.; Tilve, S. A Rapid Assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig/Diels-Alder Reaction Synlett 2011, 639-642
-
(2011)
Synlett
, pp. 639-642
-
-
Torney, P.1
Patre, R.2
Tilve, S.3
-
234
-
-
84880030658
-
An Efficient and Facile Synthesis of Iminoquinazolinedione Derivatives by Solid-State Diels-Alder Reaction under Catalyst-Free Conditions
-
Sarmah, M. M.; Bhuyan, D.; Prajapati, D. An Efficient and Facile Synthesis of Iminoquinazolinedione Derivatives by Solid-State Diels-Alder Reaction under Catalyst-Free Conditions Synlett 2013, 1667-1670
-
(2013)
Synlett
, pp. 1667-1670
-
-
Sarmah, M.M.1
Bhuyan, D.2
Prajapati, D.3
-
235
-
-
0028144422
-
Exo Diastereoselective Diels-Alder Reactions of (R)-2-Phenyl-4-methylene-oxazolidin-5-one
-
Pyne, S. G.; Safaei-G, J.; Hockless, D. C. R.; Skelton, B. W.; Sobolev, A. N.; White, A. H. Exo Diastereoselective Diels-Alder Reactions of (R)-2-Phenyl-4-methylene-oxazolidin-5-one Tetrahedron 1994, 50, 941-956
-
(1994)
Tetrahedron
, vol.50
, pp. 941-956
-
-
Pyne, S.G.1
Safaei-G, J.2
Hockless, D.C.R.3
Skelton, B.W.4
Sobolev, A.N.5
White, A.H.6
-
236
-
-
2742584946
-
Synthesis of (+)-(2 S)-2-Aminobicyclo[2.2.2]octane-2-carboxylic Acid
-
Pyne, S. G.; Safaei-G, J. Synthesis of (+)-(2 S)-2-Aminobicyclo[2.2.2]octane-2-carboxylic Acid J. Chem. Res. (Part S) 1996, 160-161
-
(1996)
J. Chem. Res. (Part S)
, pp. 160-161
-
-
Pyne, S.G.1
Safaei-G, J.2
-
237
-
-
0001245684
-
The Use of 4-Hetaryliden- and 4-Aryliden-5(4 H)-oxazolones as Dienophiles. Appropriate Reagents for the Synthesis of Cyclic Analogues of Natural Amino Acids
-
Avenoza, A.; Busto, J. H.; Paris, M.; Peregrina, J. M.; Cativiela, C. The Use of 4-Hetaryliden- and 4-Aryliden-5(4 H)-oxazolones as Dienophiles. Appropriate Reagents for the Synthesis of Cyclic Analogues of Natural Amino Acids J. Heterocycl. Chem. 1997, 34, 1099-1110
-
(1997)
J. Heterocycl. Chem.
, vol.34
, pp. 1099-1110
-
-
Avenoza, A.1
Busto, J.H.2
Paris, M.3
Peregrina, J.M.4
Cativiela, C.5
-
238
-
-
0034685901
-
New Chiral Didehydroamino Acid Derivatives from a Cyclic Glycine Template with 3,6-Dihydro-2 H -1,4-oxazin-2-one Structure: Applications to the Asymmetric Synthesis of Nonproteinogenic α-Amino Acids
-
Chinchilla, R.; Falvello, L. R.; Galindo, N.; Nájera, C. New Chiral Didehydroamino Acid Derivatives from a Cyclic Glycine Template with 3,6-Dihydro-2 H -1,4-oxazin-2-one Structure: Applications to the Asymmetric Synthesis of Nonproteinogenic α-Amino Acids J. Org. Chem. 2000, 65, 3034-3041
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3034-3041
-
-
Chinchilla, R.1
Falvello, L.R.2
Galindo, N.3
Nájera, C.4
-
239
-
-
79957777291
-
Serendipitous and Acid Catalyzed Synthesis of Spirolactones
-
Kotha, S.; Dipak, M. K.; Mobin, S. M. Serendipitous and Acid Catalyzed Synthesis of Spirolactones Tetrahedron 2011, 67, 4616-4619
-
(2011)
Tetrahedron
, vol.67
, pp. 4616-4619
-
-
Kotha, S.1
Dipak, M.K.2
Mobin, S.M.3
-
240
-
-
0000979441
-
Synthesis of Polyquinane Natural Products: An Update
-
Mehta, G.; Srikrishna, A. Synthesis of Polyquinane Natural Products: An Update Chem. Rev. 1997, 97, 671-720
-
(1997)
Chem. Rev.
, vol.97
, pp. 671-720
-
-
Mehta, G.1
Srikrishna, A.2
-
242
-
-
0000987357
-
Polycyclic Cage Compounds: Reagents, Substrates, and Materials for the 21st Century
-
Marchand, A. P. Polycyclic Cage Compounds: Reagents, Substrates, and Materials for the 21st Century Aldrichim. Acta 1995, 28, 95-104
-
(1995)
Aldrichim. Acta
, vol.28
, pp. 95-104
-
-
Marchand, A.P.1
-
243
-
-
0007669734
-
Allylation of Caged Diketones via Fragmentation Methodology
-
Kotha, S.; Manivannan, E.; Sreenivasachary, N. Allylation of Caged Diketones via Fragmentation Methodology J. Chem. Soc., Perkin Trans. 1 1999, 2845-2848
-
(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 2845-2848
-
-
Kotha, S.1
Manivannan, E.2
Sreenivasachary, N.3
-
244
-
-
84877712527
-
Recent Developments in the Retro-Diels-Alder Reaction
-
Kotha, S.; Banerjee, S. Recent Developments in the Retro-Diels-Alder Reaction RSC Adv. 2013, 3, 7642-7666
-
(2013)
RSC Adv.
, vol.3
, pp. 7642-7666
-
-
Kotha, S.1
Banerjee, S.2
-
245
-
-
33646745355
-
Retro Diels-Alder Reaction under Mild Conditions: Experimental and Theoretical Studies
-
Kotha, S.; Banerjee, S.; Patil, M. P.; Sunoj, R. B. Retro Diels-Alder Reaction under Mild Conditions: Experimental and Theoretical Studies Org. Biomol. Chem. 2006, 4, 1854-1856
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 1854-1856
-
-
Kotha, S.1
Banerjee, S.2
Patil, M.P.3
Sunoj, R.B.4
-
246
-
-
84911925642
-
Correlation between Carbon-Carbon Bond Length and the Ease of retro Diels-Alder Reaction
-
Kotha, S.; Banerjee, S.; Shaikh, M. Correlation between Carbon-Carbon Bond Length and the Ease of retro Diels-Alder Reaction J. Chem. Sci. 2014, 126, 1369-1371
-
(2014)
J. Chem. Sci.
, vol.126
, pp. 1369-1371
-
-
Kotha, S.1
Banerjee, S.2
Shaikh, M.3
-
247
-
-
84863109258
-
A Green Synthetic Route to Antimalarial and Antibacterial Agent CJ-15,801 and its Isomer Cis-CJ-15,801
-
Kashinath, K.; Swaroop, P. S.; Srinivasa Reddy, D. A Green Synthetic Route to Antimalarial and Antibacterial Agent CJ-15,801 and its Isomer Cis-CJ-15,801 RSC Adv. 2012, 2, 3596-3598
-
(2012)
RSC Adv.
, vol.2
, pp. 3596-3598
-
-
Kashinath, K.1
Swaroop, P.S.2
Srinivasa Reddy, D.3
-
248
-
-
0742321841
-
Copper-Mediated Synthesis of N -Acyl Vinylogous Carbamic Acids and Derivatives: Synthesis of the Antibiotic CJ-15,801
-
Han, C.; Shen, R.; Su, S.; Porco, J. A., Jr. Copper-Mediated Synthesis of N -Acyl Vinylogous Carbamic Acids and Derivatives: Synthesis of the Antibiotic CJ-15,801 Org. Lett. 2004, 6, 27-30
-
(2004)
Org. Lett.
, vol.6
, pp. 27-30
-
-
Han, C.1
Shen, R.2
Su, S.3
Porco, J.A.4
-
249
-
-
33846252976
-
Design and Synthesis of Spirocyclics via the Diels-Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps
-
Kotha, S.; Deb, A. C.; Chattopadhyay, S. Design and Synthesis of Spirocyclics via the Diels-Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps Lett. Org. Chem. 2006, 3, 128-134
-
(2006)
Lett. Org. Chem.
, vol.3
, pp. 128-134
-
-
Kotha, S.1
Deb, A.C.2
Chattopadhyay, S.3
-
250
-
-
33744792315
-
Design and Synthesis of Novel Propellanes by Using Claisen Rearrangement and Ring-Closing Metathesis as the Key Steps
-
Kotha, S.; Dipak, M. K. Design and Synthesis of Novel Propellanes by Using Claisen Rearrangement and Ring-Closing Metathesis as the Key Steps Chem. - Eur. J. 2006, 12, 4446-4450
-
(2006)
Chem. - Eur. J.
, vol.12
, pp. 4446-4450
-
-
Kotha, S.1
Dipak, M.K.2
-
252
-
-
84920092327
-
Design and Synthesis of Novel Bis-Annulated Caged Polycycles via Ring-Closing Metathesis: Pushpakenediol
-
Kotha, S.; Dipak, M. K. Design and Synthesis of Novel Bis-Annulated Caged Polycycles via Ring-Closing Metathesis: Pushpakenediol Beilstein J. Org. Chem. 2014, 10, 2664-2670
-
(2014)
Beilstein J. Org. Chem.
, vol.10
, pp. 2664-2670
-
-
Kotha, S.1
Dipak, M.K.2
-
253
-
-
79953078618
-
Synthesis and Reactions of a New 1,1-Disubstituted Cyclopentadiene
-
Camps, P.; Gómez, T. Synthesis and Reactions of a New 1,1-Disubstituted Cyclopentadiene ARKIVOC 2011, iii) 128-139
-
(2011)
ARKIVOC
, Issue.3
, pp. 128-139
-
-
Camps, P.1
Gómez, T.2
-
254
-
-
82955237481
-
Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes
-
Dejmek, M.; Hřebabecký, H.; Šála, M.; Dračínský, M.; Nencka, R. Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes Synthesis 2011, 4077-4083
-
(2011)
Synthesis
, pp. 4077-4083
-
-
Dejmek, M.1
Hřebabecký, H.2
Šála, M.3
Dračínský, M.4
Nencka, R.5
-
255
-
-
29844455070
-
Small-Molecule Diversity Using a Skeletal Transformation Strategy
-
Kumar, N.; Kiuchi, M.; Tallarico, J. A.; Schreiber, S. L. Small-Molecule Diversity Using a Skeletal Transformation Strategy Org. Lett. 2005, 7, 2535-2538
-
(2005)
Org. Lett.
, vol.7
, pp. 2535-2538
-
-
Kumar, N.1
Kiuchi, M.2
Tallarico, J.A.3
Schreiber, S.L.4
-
256
-
-
84978042983
-
Synthesen in der Hydroaromatischen Reihe. VIII. Mitteilung: Dien-Synthesen des Anthracens. Anthracen-Formel
-
Diels, O.; Alder, K. Synthesen in der Hydroaromatischen Reihe. VIII. Mitteilung: Dien-Synthesen des Anthracens. Anthracen-Formel Justus Liebigs Ann.Chem. 1931, 486, 191-202
-
(1931)
Justus Liebigs Ann.Chem.
, vol.486
, pp. 191-202
-
-
Diels, O.1
Alder, K.2
-
257
-
-
85178397706
-
Zur Kenntnis Mehrkerniger Aromatischer Kohlenwasserstoffe und ihrer Abkömmlinge, XI. Mitteil.: Über die Konstitution des Anthracens, II.: Bemerkungen zu einer Arbeit von Otto Diels und Kurt Alder
-
Clar, E. Zur Kenntnis Mehrkerniger Aromatischer Kohlenwasserstoffe und ihrer Abkömmlinge, XI. Mitteil.: Über die Konstitution des Anthracens, II.: Bemerkungen zu einer Arbeit von Otto Diels und Kurt Alder Ber. Dtsch. Chem. Ges. A/B 1931, 64, 2194-2200
-
(1931)
Ber. Dtsch. Chem. Ges. A/B
, vol.64
, pp. 2194-2200
-
-
Clar, E.1
-
258
-
-
0142196137
-
Diels-Alder Reactions of Anthracene, 9-Substituted Anthracenes and 9,10-Disubstituted Anthracenes
-
Atherton, J. C. C.; Jones, S. Diels-Alder Reactions of Anthracene, 9-Substituted Anthracenes and 9,10-Disubstituted Anthracenes Tetrahedron 2003, 59, 9039-9057
-
(2003)
Tetrahedron
, vol.59
, pp. 9039-9057
-
-
Atherton, J.C.C.1
Jones, S.2
-
259
-
-
0036868391
-
Synthesis of Highly Constrained Unusual α-Amino Acid Derivative by the Diels-Alder Approach
-
Kotha, S.; Ghosh, A. K.; Behera, M. Synthesis of Highly Constrained Unusual α-Amino Acid Derivative by the Diels-Alder Approach Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2002, 41B, 2330-2332
-
(2002)
Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem.
, vol.41
, pp. 2330-2332
-
-
Kotha, S.1
Ghosh, A.K.2
Behera, M.3
-
260
-
-
84929171207
-
-
(. U.S. Patent US 2005176716(A1) 2005-08-11.
-
Duan, J.; Sheppeck, J.; Jiang, B.; Gilmore, J. L. (2,3-5,6 Aryl-heteroaryl)-bicyclo(2,2,2,)octane-amide Derivatives; Antiinflammatory, Obesity, Antidiabetic Agent, Autoimmune Disease, Asthma, Arthritis; Non-Steroidal; Side Effect Reduction; Pharmacokinetics. U.S. Patent US 2005176716(A1) 2005-08-11, 2005.
-
(2005)
2,3-5,6 Aryl-heteroaryl)-bicyclo(2,2,2,)octane-amide Derivatives; Antiinflammatory, Obesity, Antidiabetic Agent, Autoimmune Disease, Asthma, Arthritis; Non-Steroidal; Side Effect Reduction; Pharmacokinetics
-
-
Duan, J.1
Sheppeck, J.2
Jiang, B.3
Gilmore, J.L.4
-
261
-
-
84929163606
-
-
U.S. Patent US 2005182083(A1) 2005-08-18.
-
Weinstein, D. S.; Sheppeck, J.; Gilmore, J. L. Heterocyclic Modulators of the Glucocorticoid Receptor, AP-1, and/or NF-kB Activity and Use Thereof. U.S. Patent US 2005182083(A1) 2005-08-18, 2005.
-
(2005)
Heterocyclic Modulators of the Glucocorticoid Receptor, AP-1, And/or NF-kB Activity and Use Thereof
-
-
Weinstein, D.S.1
Sheppeck, J.2
Gilmore, J.L.3
-
262
-
-
84929175450
-
-
U.S. Patent Appl. Publ. US 2006154973(A1) 2006-07-13.
-
Sheppeck, J.; Dhar, T. G. M.; Doweyko, L.; Gilmore, J.; Weinstein, D.; Xiao, H.-Y.; Yang, B. V.; Doweyko, A. M. Preparation of Bicyclooctanecarboxamides as Modulators of Glucocorticoid Receptor, AP-1 and NF-κB Activity and Use Thereof. U.S. Patent Appl. Publ. US 2006154973(A1) 2006-07-13, 2006.
-
(2006)
Preparation of Bicyclooctanecarboxamides As Modulators of Glucocorticoid Receptor, AP-1 and NF-κB Activity and Use Thereof
-
-
Sheppeck, J.1
Dhar, T.G.M.2
Doweyko, L.3
Gilmore, J.4
Weinstein, D.5
Xiao, H.-Y.6
Yang, B.V.7
Doweyko, A.M.8
-
265
-
-
84929175209
-
-
U.S. Patent US 7605264(B2) 2009-10-20.
-
Weinstein, D. S.; Sheppeck, J.; Gilmore, J. L. Preparation of Heterocyclic Bicyclooctylcarboxamide Derivatives as Modulators of Glucocorticoid Receptor, AP-1, and/or NF-κB. U.S. Patent US 7605264(B2) 2009-10-20, 2009.
-
(2009)
Preparation of Heterocyclic Bicyclooctylcarboxamide Derivatives As Modulators of Glucocorticoid Receptor, AP-1, And/or NF-κB
-
-
Weinstein, D.S.1
Sheppeck, J.2
Gilmore, J.L.3
-
266
-
-
84929158117
-
-
U.S. Patent US 7569689(B2) 2009-08-04.
-
Duan, J.; Jiang, B.; Sheppeck, J.; Gilmore, J. L. Fused Aryl and Heteroaryl Bicyclo[2.2.2]octane Derivative Modulators of the Glucocorticoid Receptor, AP-1, and/or NF-κB Activity, and Therapeutic Use Thereof. U.S. Patent US 7569689(B2) 2009-08-04, 2009.
-
(2009)
Fused Aryl and Heteroaryl Bicyclo[2.2.2]octane Derivative Modulators of the Glucocorticoid Receptor, AP-1, And/or NF-κB Activity, and Therapeutic Use Thereof
-
-
Duan, J.1
Jiang, B.2
Sheppeck, J.3
Gilmore, J.L.4
-
267
-
-
15944420883
-
Highly Regioselective Diels-Alder Reactions of 9-Substituted Anthracenes and 2-Acetamidoacrylate: Synthesis of Conformationally Constrained α-Amino Acids
-
Yang, B. V.; Doweyko, L. M. Highly Regioselective Diels-Alder Reactions of 9-Substituted Anthracenes and 2-Acetamidoacrylate: Synthesis of Conformationally Constrained α-Amino Acids Tetrahedron Lett. 2005, 46, 2857-2860
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2857-2860
-
-
Yang, B.V.1
Doweyko, L.M.2
-
269
-
-
84927923697
-
Synthesis of Conformationally Constrained α-Amino Acid Derivatives Containing Bicyclo[2.2.2]octane Unit via the Diels-Alder Reaction and the Suzuki-Miyaura Cross-Coupling as Key Steps
-
Kotha, S.; Meshram, M.; Muthusamy, G. Synthesis of Conformationally Constrained α-Amino Acid Derivatives Containing Bicyclo[2.2.2]octane Unit via the Diels-Alder Reaction and the Suzuki-Miyaura Cross-Coupling as Key Steps Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2015, 54B, 505-513
-
(2015)
Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem.
, vol.54
, pp. 505-513
-
-
Kotha, S.1
Meshram, M.2
Muthusamy, G.3
-
270
-
-
84923283740
-
Design and Synthesis of Conformationally Constrained Bicyclo[2.2.2]octane-Based Unusual α-Amino Acid Derivatives via the Diels-Alder Reaction
-
Kotha, S.; Meshram, M. Design and Synthesis of Conformationally Constrained Bicyclo[2.2.2]octane-Based Unusual α-Amino Acid Derivatives via the Diels-Alder Reaction Heterocycles 2015, 90, 357-371
-
(2015)
Heterocycles
, vol.90
, pp. 357-371
-
-
Kotha, S.1
Meshram, M.2
-
271
-
-
84891333201
-
Functionalization of Anthracene by Strategic Utilization of the Diels-Alder Reaction and the Ring-Closing Metathesis
-
Kotha, S.; Meshram, M. Functionalization of Anthracene by Strategic Utilization of the Diels-Alder Reaction and the Ring-Closing Metathesis J. Indian Chem. Soc. 2013, 90, 1789-1794
-
(2013)
J. Indian Chem. Soc.
, vol.90
, pp. 1789-1794
-
-
Kotha, S.1
Meshram, M.2
-
272
-
-
84887075869
-
Diels-Alder Reactions of 9-Ferrocenyl- and 9,10-Diferrocenylanthracene: Steric Control of 9,10-versus 1,4-Cycloaddition
-
Nikitin, K.; Müller-Bunz, H.; McGlinchey, M. J. Diels-Alder Reactions of 9-Ferrocenyl- and 9,10-Diferrocenylanthracene: Steric Control of 9,10-versus 1,4-Cycloaddition Organometallics 2013, 32, 6118-6129
-
(2013)
Organometallics
, vol.32
, pp. 6118-6129
-
-
Nikitin, K.1
Müller-Bunz, H.2
McGlinchey, M.J.3
-
273
-
-
84865517099
-
Using Light and a Molecular Switch to 'Lock' and 'Unlock' the Diels-Alder Reaction
-
Erno, Z.; Asadirad, A. M.; Lemieux, V.; Branda, N. R. Using Light and a Molecular Switch to 'Lock' and 'Unlock' the Diels-Alder Reaction Org. Biomol. Chem. 2012, 10, 2787-2792
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 2787-2792
-
-
Erno, Z.1
Asadirad, A.M.2
Lemieux, V.3
Branda, N.R.4
-
274
-
-
84884533615
-
Towards Molecular Ribbons of Corannulene
-
Furrer, F.; Linden, A.; Stuparu, M. C. Towards Molecular Ribbons of Corannulene Chem. - Eur. J. 2013, 19, 13199-13206
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 13199-13206
-
-
Furrer, F.1
Linden, A.2
Stuparu, M.C.3
-
275
-
-
70349787847
-
In Situ Enamine Activation in Aqueous Salt Solutions: Highly Efficient Asymmetric Organocatalytic Diels-Alder Reaction of Cyclohexenones with Nitroolefins
-
Xu, D.-Q.; Xia, A.-B.; Luo, S.-P.; Tang, J.; Zhang, S.; Jiang, J.-R.; Xu, Z.-Y. In Situ Enamine Activation in Aqueous Salt Solutions: Highly Efficient Asymmetric Organocatalytic Diels-Alder Reaction of Cyclohexenones with Nitroolefins Angew. Chem., Int. Ed. 2009, 48, 3821-3824
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 3821-3824
-
-
Xu, D.-Q.1
Xia, A.-B.2
Luo, S.-P.3
Tang, J.4
Zhang, S.5
Jiang, J.-R.6
Xu, Z.-Y.7
-
276
-
-
84864259502
-
Diels-Alder Cycloaddition of Acetylene Gas to a Polycyclic Aromatic Hydrocarbon Bay Region
-
Fort, E. H.; Jeffreys, M. S.; Scott, L. T. Diels-Alder Cycloaddition of Acetylene Gas to a Polycyclic Aromatic Hydrocarbon Bay Region Chem. Commun. 2012, 48, 8102-8104
-
(2012)
Chem. Commun.
, vol.48
, pp. 8102-8104
-
-
Fort, E.H.1
Jeffreys, M.S.2
Scott, L.T.3
-
277
-
-
84883471350
-
An Electron Rich Porous Extended Framework as a Heterogeneous Catalyst for Diels-Alder Reactions
-
Gole, B.; Bar, A. K.; Mallick, A.; Banerjee, R.; Mukherjee, P. S. An Electron Rich Porous Extended Framework as a Heterogeneous Catalyst for Diels-Alder Reactions Chem. Commun. 2013, 49, 7439-7441
-
(2013)
Chem. Commun.
, vol.49
, pp. 7439-7441
-
-
Gole, B.1
Bar, A.K.2
Mallick, A.3
Banerjee, R.4
Mukherjee, P.S.5
-
278
-
-
84861227809
-
Synthesis of Tetrahydroanthracen-9-ones by the Domino Aldol Condensation/Diels-Alder Cycloaddition
-
Chang, M.-Y.; Wu, M.-H. Synthesis of Tetrahydroanthracen-9-ones by the Domino Aldol Condensation/Diels-Alder Cycloaddition Tetrahedron Lett. 2012, 53, 3173-3177
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 3173-3177
-
-
Chang, M.-Y.1
Wu, M.-H.2
-
279
-
-
84881242218
-
Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/aza-Michael/Aldol Condensation Domino Reaction
-
Enders, D.; Joie, C.; Deckers, K. Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/aza-Michael/Aldol Condensation Domino Reaction Chem. - Eur. J. 2013, 19, 10818-10821
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 10818-10821
-
-
Enders, D.1
Joie, C.2
Deckers, K.3
-
280
-
-
84894089672
-
Efficient One-Pot Synthesis of Novel and Diverse Tetrahydroquinolines Bearing Pyranopyrazoles Using Organocatalyzed Domino Knoevenagel/Hetero Diels-Alder Reactions
-
Pandit, R. P.; Lee, Y. R. Efficient One-Pot Synthesis of Novel and Diverse Tetrahydroquinolines Bearing Pyranopyrazoles Using Organocatalyzed Domino Knoevenagel/Hetero Diels-Alder Reactions Mol. Divers. 2014, 18, 39-50
-
(2014)
Mol. Divers.
, vol.18
, pp. 39-50
-
-
Pandit, R.P.1
Lee, Y.R.2
-
281
-
-
84862016521
-
Synthesis of Heterocycles by Domino-Knoevenagel/Hetero-Diels-Alder Reactions
-
Majumdar, K. C.; Taher, A.; Nandi, R. K. Synthesis of Heterocycles by Domino-Knoevenagel/Hetero-Diels-Alder Reactions Tetrahedron 2012, 68, 5693-5718
-
(2012)
Tetrahedron
, vol.68
, pp. 5693-5718
-
-
Majumdar, K.C.1
Taher, A.2
Nandi, R.K.3
-
282
-
-
84883817262
-
A Four-Step Domino Knoevenagel/Hetero-Diels-Alder Reaction
-
Bryhas, A. O.; Matiychuk, V. S.; Lis, T.; Kinzhybalo, V.; Smalius, V. V.; Obushaka, M. D. A Four-Step Domino Knoevenagel/Hetero-Diels-Alder Reaction Tetrahedron Lett. 2013, 54, 5667-5670
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 5667-5670
-
-
Bryhas, A.O.1
Matiychuk, V.S.2
Lis, T.3
Kinzhybalo, V.4
Smalius, V.V.5
Obushaka, M.D.6
-
283
-
-
34547661989
-
Sequential Diels-Alder and Cobalt Octacarbonyl Catalyzed Pauson-Khand Reactions in the Formation of Polycyclic Enones
-
Choi, S. Y.; Lee, S. I.; Park, K. H.; Chung, Y. K. Sequential Diels-Alder and Cobalt Octacarbonyl Catalyzed Pauson-Khand Reactions in the Formation of Polycyclic Enones Synlett 2007, 1857-1862
-
(2007)
Synlett
, pp. 1857-1862
-
-
Choi, S.Y.1
Lee, S.I.2
Park, K.H.3
Chung, Y.K.4
-
284
-
-
69249237012
-
Synthesis of Substituted Fused Pyridines, Pyrazines and Pyrimidines by Sequential Ugi/Inverse Electron Demand Diels-Alder Transformations
-
Akritopoulou-Zanze, I.; Wang, Y.; Zhao, H.; Djuric, S. W. Synthesis of Substituted Fused Pyridines, Pyrazines and Pyrimidines by Sequential Ugi/Inverse Electron Demand Diels-Alder Transformations Tetrahedron Lett. 2009, 50, 5773-5776
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5773-5776
-
-
Akritopoulou-Zanze, I.1
Wang, Y.2
Zhao, H.3
Djuric, S.W.4
-
285
-
-
78449248941
-
Platinum(II) Chloride-Catalyzed Stereoselective Domino Enyne Isomerization/Diels-Alder Reaction
-
Schelwies, M.; Farwick, A.; Rominger, F.; Helmchen, G. Platinum(II) Chloride-Catalyzed Stereoselective Domino Enyne Isomerization/Diels-Alder Reaction J. Org. Chem. 2010, 75, 7917-7919
-
(2010)
J. Org. Chem.
, vol.75
, pp. 7917-7919
-
-
Schelwies, M.1
Farwick, A.2
Rominger, F.3
Helmchen, G.4
-
286
-
-
84897547945
-
Intramolecular Diels-Alder Reaction as a Key Step in Tandem or Sequential Processes: A Versatile Tool for the Synthesis of Fused and Bridged Bicyclic or Polycyclic Compounds
-
Parvatkar, P. T.; Kadamb, H. K.; Tilve, S. G. Intramolecular Diels-Alder Reaction as a Key Step in Tandem or Sequential Processes: A Versatile Tool for the Synthesis of Fused and Bridged Bicyclic or Polycyclic Compounds Tetrahedron 2014, 70, 2857-2888
-
(2014)
Tetrahedron
, vol.70
, pp. 2857-2888
-
-
Parvatkar, P.T.1
Kadamb, H.K.2
Tilve, S.G.3
-
287
-
-
84887530181
-
[3]Dendralene Synthesis: Rhodium(III)-Catalyzed Alkenyl C-H Activation and Coupling Reaction with Allenyl Carbinol Carbonate
-
Wang, H.; Beiring, B.; Yu, D.-G.; Collins, K. D.; Glorius, F. [3]Dendralene Synthesis: Rhodium(III)-Catalyzed Alkenyl C-H Activation and Coupling Reaction with Allenyl Carbinol Carbonate Angew. Chem., Int. Ed. 2013, 52, 12430-12434
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 12430-12434
-
-
Wang, H.1
Beiring, B.2
Yu, D.-G.3
Collins, K.D.4
Glorius, F.5
-
288
-
-
84896767011
-
Rh(III)-Catalyzed C-H Activation with Allenes to Synthesize Conjugated Olefins
-
Gong, T.-J.; Su, W.; Liu, Z.-J.; Cheng, W.-M.; Xiao, B.; Fu, Y. Rh(III)-Catalyzed C-H Activation with Allenes to Synthesize Conjugated Olefins Org. Lett. 2014, 16, 330-333
-
(2014)
Org. Lett.
, vol.16
, pp. 330-333
-
-
Gong, T.-J.1
Su, W.2
Liu, Z.-J.3
Cheng, W.-M.4
Xiao, B.5
Fu, Y.6
|