-
1
-
-
6044269452
-
In the golden age of organocatalysis
-
Dalko PI, Moisan L. In the golden age of organocatalysis. Angew Chem Int Ed Engl 2004;43:5138-5175.
-
(2004)
Angew Chem Int Ed Engl
, vol.43
, pp. 5138-5175
-
-
Dalko, P.I.1
Moisan, L.2
-
2
-
-
33748766864
-
The organic approach to asymmetric catalysis
-
List B, Yang JW. The organic approach to asymmetric catalysis. Science 2006;313:1584-1586.
-
(2006)
Science
, vol.313
, pp. 1584-1586
-
-
List, B.1
Yang, J.W.2
-
5
-
-
34547623607
-
Asymmetric organocatalysis
-
Pellissier H. Asymmetric organocatalysis. Tetrahedron 2007;63:9267-9331.
-
(2007)
Tetrahedron
, vol.63
, pp. 9267-9331
-
-
Pellissier, H.1
-
6
-
-
48849094479
-
Asymmetric organocatalysis: From infancy to adolescence
-
Dondoni A, Massi A. Asymmetric organocatalysis: from infancy to adolescence. Angew Chem Int Ed Engl 2008;47:4638-4660.
-
(2008)
Angew Chem Int Ed Engl
, vol.47
, pp. 4638-4660
-
-
Dondoni, A.1
Massi, A.2
-
8
-
-
48649106016
-
Hydrogen-Bond-Mediated asymmetric catalysis
-
Yu X, Wang W. Hydrogen-Bond-Mediated asymmetric catalysis. Chem Asian J 2008;3:516-532.
-
(2008)
Chem Asian J
, vol.3
, pp. 516-532
-
-
Yu, X.1
Wang, W.2
-
9
-
-
38349135345
-
Small-molecule H-bond donors in asymmetric catalysis
-
Doyle AG, Jacobsen EN. Small-molecule H-bond donors in asymmetric catalysis. Chem Rev 2007;107:5713-5743.
-
(2007)
Chem Rev
, vol.107
, pp. 5713-5743
-
-
Doyle, A.G.1
Jacobsen, E.N.2
-
10
-
-
51749120761
-
Organocatalytic asymmetric synthesis of α,α-disubstituted α-amino acids and derivatives
-
Cabrera S, Reyes E, Alemán J, Milelli A, Kobbelgaard S, Jørgensen KA. Organocatalytic asymmetric synthesis of α,α-disubstituted α-amino acids and derivatives. J Am Chem Soc 2008;130:12031-12037.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 12031-12037
-
-
Cabrera, S.1
Reyes, E.2
Alemán, J.3
Milelli, A.4
Kobbelgaard, S.5
Jørgensen, K.A.6
-
11
-
-
67649600829
-
Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: Application to the formal synthesis of (+)-physostigmine
-
Bui T, Syed S, Barbas CF III. Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine. J Am Chem Soc 2009;131:8758-8759.
-
(2009)
J Am Chem Soc
, vol.131
, pp. 8758-8759
-
-
Bui, T.1
Syed, S.2
Barbas III, C.F.3
-
12
-
-
55249084647
-
Enantioselective organocatalytic approach to γ-methylene-δ- lactones and δ-lactams
-
Albrecht Ł, Richter B, Krawczyk H, Jørgensen KA. Enantioselective organocatalytic approach to γ-methylene-δ-lactones and δ-lactams. J Org Chem 2008;73:8337-8343.
-
(2008)
J Org Chem
, vol.73
, pp. 8337-8343
-
-
Albrecht, Ł.1
Richter, B.2
Krawczyk, H.3
Jørgensen, K.A.4
-
14
-
-
34247472031
-
Enantioselective and diastereoselective Michael addition of ketone/aldehyde to trans-nitroolefins catalyzed by a novel chiral pyrrolidine-thiourea
-
DOI 10.1002/chir.20382
-
Shen Z, Zhang Y, Jiao C, Li B, Ding J, Zhang Y. Enantioselective and diastereoselective Michael addition of ketone/aldehyde to trans-nitroolefins catalyzed by a novel chiral pyrrolidine-thiourea. Chirality 2007;19:307-312. (Pubitemid 46659344)
-
(2007)
Chirality
, vol.19
, Issue.4
, pp. 307-312
-
-
Shen, Z.1
Zhang, Y.2
Jiao, C.3
Li, B.4
Ding, J.5
Zhang, Y.6
-
16
-
-
33746643770
-
Pyrroliding-thiourea as a bifunctional organocatalyst: Highly enantioselective Michael addition of cyclohexanone to nitroolefins
-
Cao CL, Ye MC, Sun XL, Tang Y. Pyrroliding-thiourea as a bifunctional organocatalyst: highly enantioselective Michael addition of cyclohexanone to nitroolefins. Org Lett 2006;8:2901-2904.
-
(2006)
Org Lett
, vol.8
, pp. 2901-2904
-
-
Cao, C.L.1
Ye, M.C.2
Sun, X.L.3
Tang, Y.4
-
17
-
-
66149154333
-
Rational design of organocatalyst: Highly stereoselective Michael addition of cyclic ketones to nitroolefins
-
Tan B, Zeng X, Lu Y, Chua PJ, Zhong G. Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins. Org Lett 2009;11:1927-1930.
-
(2009)
Org Lett
, vol.11
, pp. 1927-1930
-
-
Tan, B.1
Zeng, X.2
Lu, Y.3
Chua, P.J.4
Zhong, G.5
-
18
-
-
14844316261
-
Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes
-
DOI 10.1002/anie.200461959
-
Wang W, Wang J, Li H. Direct, highly enantioselective pyrrolidine sulfonamide catalyzed Michael addition of aldehydes to nitrostyrenes. Angew Chem Int Ed Engl 2005;44:1369-1371. (Pubitemid 40343551)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.9
, pp. 1369-1371
-
-
Wang, W.1
Wang, J.2
Li, H.3
-
19
-
-
33746620447
-
A recyclable flurous (S)-pyrrolidine sulfonamide promoted direct, highly enantioselective Michael addition of ketones and aldehydes to nitroolefins in water
-
Zu L, Wang J, Li H, Wang W. A recyclable flurous (S)-pyrrolidine sulfonamide promoted direct, highly enantioselective Michael addition of ketones and aldehydes to nitroolefins in water. Org Lett 2006;8:3077-3079.
-
(2006)
Org Lett
, vol.8
, pp. 3077-3079
-
-
Zu, L.1
Wang, J.2
Li, H.3
Wang, W.4
-
20
-
-
63849130528
-
Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: Uses of fluorinated methines as nucleophiles
-
Han X, Luo J, Liu C, Lu Y. Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: uses of fluorinated methines as nucleophiles. Chem Commun 2009;2044-2046.
-
(2009)
Chem Commun
, pp. 2044-2046
-
-
Han, X.1
Luo, J.2
Liu, C.3
Lu, Y.4
-
21
-
-
53849136278
-
Novel bifunctional chiral urea and thiourea derivatives as organocatalysts: Enantioselective nitro-Michael Reaction of malonates and diketones
-
Andrés JM, Manzano R, Pedrosa R. Novel bifunctional chiral urea and thiourea derivatives as organocatalysts: enantioselective nitro-Michael Reaction of malonates and diketones. Chem Eur J 2008;14: 5116-5119.
-
(2008)
Chem Eur J
, vol.14
, pp. 5116-5119
-
-
Andrés, J.M.1
Manzano, R.2
Pedrosa, R.3
-
22
-
-
65949105703
-
Enantioselective organocatalytic Michael addition of aldehydes to β-nitrostyrenes
-
Laars M, Ausmees K, Uudsemaa M, Tamm T, Kanger T, Lopp M. Enantioselective organocatalytic Michael addition of aldehydes to β-nitrostyrenes. J Org Chem 2009;74:3772-3775.
-
(2009)
J Org Chem
, vol.74
, pp. 3772-3775
-
-
Laars, M.1
Ausmees, K.2
Uudsemaa, M.3
Tamm, T.4
Kanger, T.5
Lopp, M.6
-
23
-
-
62949181205
-
Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides
-
Zhang X, Liu S, Li X, Yan M, Chan ASC. Highly enantioselective conjugate addition of aldehydes to nitroolefins catalyzed by chiral bifunctional sulfamides. Chem Commun 2009;833-835.
-
(2009)
Chem Commun
, pp. 833-835
-
-
Zhang, X.1
Liu, S.2
Li, X.3
Yan, M.4
Chan, A.S.C.5
-
24
-
-
70349782136
-
Bifunctional guanidine via an amino amide skeleton for asymmetric Michael ractions of β-ketoesters with nitroolefins: A concise synthesis of bicyclic b-amino acids
-
Yu Z, Liu X, Zhou L, Lin L, Feng X. Bifunctional guanidine via an amino amide skeleton for asymmetric Michael ractions of β-ketoesters with nitroolefins: A concise synthesis of bicyclic b-amino acids. Angew Chem Int Ed Engl 2009;48:5195-5198.
-
(2009)
Angew Chem Int Ed Engl
, vol.48
, pp. 5195-5198
-
-
Yu, Z.1
Liu, X.2
Zhou, L.3
Lin, L.4
Feng, X.5
-
25
-
-
67649639592
-
L-Prolinol as a highly enantioselective catalyst for Michael addition of cyclohexanone to nitroole-fins
-
Chua PJ, Tan B, Zeng XF, Zhong GF. L-Prolinol as a highly enantioselective catalyst for Michael addition of cyclohexanone to nitroole-fins. Bioorg Med Chem Lett 2009;19:3915-3918.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 3915-3918
-
-
Chua, P.J.1
Tan, B.2
Zeng, X.F.3
Zhong, G.F.4
-
26
-
-
67650074168
-
Prolinol sulfinyl ester derivatives: Organocatalytic Michael addition of ketones to nitroolefins under neat conditions
-
Zeng XF, Zhong GF. Prolinol sulfinyl ester derivatives: organocatalytic Michael addition of ketones to nitroolefins under neat conditions. Synthesis 2009;9:1545-1550.
-
(2009)
Synthesis
, vol.9
, pp. 1545-1550
-
-
Zeng, X.F.1
Zhong, G.F.2
-
27
-
-
57149148424
-
Organocatalyzed highly enantioselective Michael additions of malonates to enones by using novel primary-secondary diamine catalysts
-
Yang YQ, Zhao G. Organocatalyzed highly enantioselective Michael additions of malonates to enones by using novel primary-secondary diamine catalysts. Chem Eur J 2008;14:10888-10891.
-
(2008)
Chem Eur J
, vol.14
, pp. 10888-10891
-
-
Yang, Y.Q.1
Zhao, G.2
-
28
-
-
0141563562
-
Asymmetric Michael addition of α-hydroxyketones to nitroolefins catalyzed by chiral diamine
-
DOI 10.1021/ol0348755
-
Andrey O, Alexakis A, Bernardinelli G. Asymmetric Michael addition of α-hydroxyketones to nitroolefins catalyzed by chiral diamine. Org Lett 2003;5:2559-2561. (Pubitemid 37140907)
-
(2003)
Organic Letters
, vol.5
, Issue.14
, pp. 2559-2561
-
-
Andrey, O.1
Alexakis, A.2
Bernardinelli, G.3
-
29
-
-
0035891780
-
Catalytic direct asymmetric Michael reactions: Taming naked aldehyde donors
-
Betancort JM, Barbas CF III. Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors. Org Lett 2001;3:3737-3740.
-
(2001)
Org Lett
, vol.3
, pp. 3737-3740
-
-
Betancort, J.M.1
Barbas III, C.F.2
-
30
-
-
0141425514
-
Organocatalytic Michael addition, a convenient tool in total synthesis. First asymmetric synthesis of (-)-botryodiplodin
-
Andrey O, Vidonne A, Alexakis A. Organocatalytic Michael addition, a convenient tool in total synthesis. First asymmetric synthesis of (-)-botryodiplodin. Tetrahedron Lett 2003;44:7901-7904.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 7901-7904
-
-
Andrey, O.1
Vidonne, A.2
Alexakis, A.3
-
31
-
-
4043184288
-
Direct asymmetric organocatalytic Michael reactions of α,α-disubstituted aldehydes with β-nitrostyrenes for the synthesis of quaternary carbon-containing products
-
Mase N, Thayumanavan R, Tanaka F, Barbas CF. Direct asymmetric organocatalytic Michael reactions of α,α-disubstituted aldehydes with β-nitrostyrenes for the synthesis of quaternary carbon-containing products. Org Lett 2004;6:2527-2530.
-
(2004)
Org Lett
, vol.6
, pp. 2527-2530
-
-
Mase, N.1
Thayumanavan, R.2
Tanaka, F.3
Barbas, C.F.4
-
32
-
-
33947605163
-
Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins
-
Vishnumaya VK. Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins. Org Lett 2007;9:1117-1119.
-
(2007)
Org Lett
, vol.9
, pp. 1117-1119
-
-
Vishnumaya, V.K.1
-
33
-
-
33746596576
-
Simple diamine- And triamine-protonic acid catalysts for the enantioselective Michael addition of cyclic ketones to nitroalkenes
-
DOI 10.1021/ja062701n
-
Pansare SV, Pandya K. Simple diamine- and triamine-protonic acid catalysts for the enantioselective Michael addition of cyclic ketones to nitroalkenes. J Am Chem Soc 2006;128:9624-9625. (Pubitemid 44147934)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.30
, pp. 9624-9625
-
-
Pansare, S.V.1
Pandya, K.2
-
34
-
-
33646142092
-
Organocatalytic direct Michael reaction of ketones and aldehydes with β-nitrostyrene in brine
-
Mase N, Watanabe K, Yoda H, Takabe K, Tanaka F, Barbas CF. Organocatalytic direct Michael reaction of ketones and aldehydes with β-nitrostyrene in brine. J Am Chem Soc 2006;128:4966-4967.
-
(2006)
J Am Chem Soc
, vol.128
, pp. 4966-4967
-
-
Mase, N.1
Watanabe, K.2
Yoda, H.3
Takabe, K.4
Tanaka, F.5
Barbas, C.F.6
-
35
-
-
53849091017
-
Diversity-oriented synthesis towards conceptually new highly modular aminal-pyrrolidine organocatalysts
-
Quintard A, Bournaud C, Alexakis A. Diversity-oriented synthesis towards conceptually new highly modular aminal-pyrrolidine organocatalysts. Chem Eur J 2008;14:7504-7507.
-
(2008)
Chem Eur J
, vol.14
, pp. 7504-7507
-
-
Quintard, A.1
Bournaud, C.2
Alexakis, A.3
-
36
-
-
4143095871
-
Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents
-
List B. Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents. Acc Chem Res 2004;37:548-557.
-
(2004)
Acc Chem Res
, vol.37
, pp. 548-557
-
-
List, B.1
-
37
-
-
4143114533
-
Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-Alder reactions
-
Notz W, Tanaka F, Barbas CF. Enamine-based organocatalysis with proline and diamines: The development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-Alder reactions. Acc Chem Res 2004;37:580-591.
-
(2004)
Acc Chem Res
, vol.37
, pp. 580-591
-
-
Notz, W.1
Tanaka, F.2
Barbas, C.F.3
-
38
-
-
65449148970
-
Secondary-secondary diamine catalysts for the enantioselective Michael addition of cyclic ketones to nitroalkenes
-
Pansare SV, Kirby RL. Secondary-secondary diamine catalysts for the enantioselective Michael addition of cyclic ketones to nitroalkenes. Tetrahedron 2009;65:4557-4561.
-
(2009)
Tetrahedron
, vol.65
, pp. 4557-4561
-
-
Pansare, S.V.1
Kirby, R.L.2
-
39
-
-
0000761777
-
Efficient proline-catalyzed Michael additions of unmodified ketones to nitroolefins
-
List B, Pojarliev P, Martin HJ. Efficient proline-catalyzed Michael additions of unmodified ketones to nitroolefins. Org Lett 2001;3:2423-2425.
-
(2001)
Org Lett
, vol.3
, pp. 2423-2425
-
-
List, B.1
Pojarliev, P.2
Martin, H.J.3
-
41
-
-
0043204564
-
Synthesis and application to asymmetric allylic amination of substituted monodonor diazaphospholidine ligands
-
Edwards CW, Shipton MR, Alcock NW, Clasea H, Willsa M. Synthesis and application to asymmetric allylic amination of substituted monodonor diazaphospholidine ligands. Tetrahedron 2003;59:6473-6480.
-
(2003)
Tetrahedron
, vol.59
, pp. 6473-6480
-
-
Edwards, C.W.1
Shipton, M.R.2
Alcock, N.W.3
Clasea, H.4
Willsa, M.5
-
42
-
-
0002824073
-
Synthesis and characterization of new chiral Rh(I) complexes with N,N′-, and N,P-ligands. A study of anchoring on the modified zeolites and catalytic properties of heterogenized complexes
-
Carmona A, Corma A, Iglesias M, San José A, Sánchez F. Synthesis and characterization of new chiral Rh(I) complexes with N,N′-, and N,P-ligands. A study of anchoring on the modified zeolites and catalytic properties of heterogenized complexes. J Organomet Chem 1995;492:11-21.
-
(1995)
J Organomet Chem
, vol.492
, pp. 11-21
-
-
Carmona, A.1
Corma, A.2
Iglesias, M.3
San José, A.4
Sánchez, F.5
-
44
-
-
0006059147
-
Photochemical isomerization and dimerization of 1-(9-anthryl)-2- nitroethylene
-
Becker HD, Sörensen H, Sandros K. Photochemical isomerization and dimerization of 1-(9-anthryl)-2-nitroethylene. J Org Chem 1986;51:3223-3226.
-
(1986)
J Org Chem
, vol.51
, pp. 3223-3226
-
-
Becker, H.D.1
Sörensen, H.2
Sandros, K.3
-
45
-
-
0004825486
-
Mescaline analogs. V. p-dialkylamino-β-phenethylamines and 9-(β-aminoethyl)julolidine
-
Benington F, Morin RD, Clark LC. Mescaline analogs. V. p-dialkylamino-β-phenethylamines and 9-(β-aminoethyl)julolidine. J Org Chem 1956;21:1470-1472.
-
(1956)
J Org Chem
, vol.21
, pp. 1470-1472
-
-
Benington, F.1
Morin, R.D.2
Clark, L.C.3
-
46
-
-
1942469514
-
Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives
-
DOI 10.1073/pnas.0307176101
-
Tang Z, Jiang F, Cui X, Gong LZ, Mi AQ, Jiang YZ, Wu YD. Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives. Proc Natl Acad Sci USA 2004;101:5755-5760. (Pubitemid 38520473)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.16
, pp. 5755-5760
-
-
Tang, Z.1
Jiang, F.2
Cui, X.3
Gong, L.-Z.4
Mi, A.-Q.5
Jiang, Y.-Z.6
Wu, Y.-D.7
-
47
-
-
0034853451
-
Functionalization of calyx[4]-arenes at the lower rim and synthesis of calyx[4](aza)crowns
-
Chen CF, Zheng QY, Zheng YS, Huang ZT. Functionalization of calyx[4]-arenes at the lower rim and synthesis of calyx[4](aza)crowns. Syn Commun 2002;31:2829-2836.
-
(2002)
Syn Commun
, vol.31
, pp. 2829-2836
-
-
Chen, C.F.1
Zheng, Q.Y.2
Zheng, Y.S.3
Huang, Z.T.4
-
48
-
-
33645915448
-
Design of highly enantioselective organocatalysts based on molecular recognition
-
Tang Z, Cun LF, Cui X, Mi AQ, Jiang YZ, Gong LZ. Design of highly enantioselective organocatalysts based on molecular recognition. Org Lett 2006;8:1263-1266.
-
(2006)
Org Lett
, vol.8
, pp. 1263-1266
-
-
Tang, Z.1
Cun, L.F.2
Cui, X.3
Mi, A.Q.4
Jiang, Y.Z.5
Gong, L.Z.6
-
49
-
-
0001013917
-
Asymmetric synthesis based on chiral diamines having pyrrolidine ring
-
Mukaiyama T. Asymmetric synthesis based on chiral diamines having pyrrolidine ring. Tetrahedron 1981;37:4111-4119.
-
(1981)
Tetrahedron
, vol.37
, pp. 4111-4119
-
-
Mukaiyama, T.1
-
50
-
-
0025327884
-
Asymmetric transformation of symmetrical epoxides to allylic alcohols by lithium (S)-2-(N,N-disubstituted aminomethyl)- pyrrolidine
-
Isalasami M. Asymmetric transformation of symmetrical epoxides to allylic alcohols by lithium (S)-2-(N,N-disubstituted aminomethyl)- pyrrolidine. Bull Chem Soc Jpn 1990;63:721-727.
-
(1990)
Bull Chem Soc Jpn
, vol.63
, pp. 721-727
-
-
Isalasami, M.1
-
51
-
-
33751407719
-
Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts
-
DOI 10.1016/j.tetlet.2006.11.037, PII S0040403906022520
-
Cao YJ, Lai YY, Wang X, Li YJ, Xiao WJ. Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts. Tetrahedron Lett 2007;48:21-24. (Pubitemid 44821295)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.1
, pp. 21-24
-
-
Cao, Y.-J.1
Lai, Y.-Y.2
Wang, X.3
Li, Y.-J.4
Xiao, W.-J.5
-
52
-
-
44949202349
-
A chiral thioureido acid as an effective additive for enantioselective organocatalytic Michael additions of nitroolefins
-
Xu DQ, Yue HD, Luo SP, Xia AB, Zhang S, Xu ZY. A chiral thioureido acid as an effective additive for enantioselective organocatalytic Michael additions of nitroolefins. Org Biomol Chem 2008;6:2054-2057.
-
(2008)
Org Biomol Chem
, vol.6
, pp. 2054-2057
-
-
Xu, D.Q.1
Yue, H.D.2
Luo, S.P.3
Xia, A.B.4
Zhang, S.5
Xu, Z.Y.6
-
53
-
-
54749140370
-
Modularly designed organocatalytic assemblies for direct nitro-Michael addition reactions
-
Mandal T, Zhao CG. Modularly designed organocatalytic assemblies for direct nitro-Michael addition reactions. Angew Chem Int Ed Engl 2008;47:7714-7717.
-
(2008)
Angew Chem Int Ed Engl
, vol.47
, pp. 7714-7717
-
-
Mandal, T.1
Zhao, C.G.2
-
54
-
-
38949133131
-
Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water
-
DOI 10.1002/anie.200704161
-
Zhu S, Yu S, Ma D. Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water. Angew Chem Int Ed Engl 2008;47:545-548. (Pubitemid 351412339)
-
(2008)
Angewandte Chemie - International Edition
, vol.47
, Issue.3
, pp. 545-548
-
-
Zhu, S.1
Yu, S.2
Ma, D.3
-
55
-
-
33846254547
-
Combining proline and 'click chemistry': A class of versatile organocatalysts for the highly diastereo- and enantioselective Michael addition in water
-
Yan ZY, Niu YN, Wei HL, Wu LY, Zhao YB, Liang YM. Combining proline and 'click chemistry': a class of versatile organocatalysts for the highly diastereo- and enantioselective Michael addition in water. Tetrahedron Asymmetry 2006;17:3288-3293.
-
(2006)
Tetrahedron Asymmetry
, vol.17
, pp. 3288-3293
-
-
Yan, Z.Y.1
Niu, Y.N.2
Wei, H.L.3
Wu, L.Y.4
Zhao, Y.B.5
Liang, Y.M.6
-
56
-
-
34848859862
-
Highly enantioselective Michael additions in water catalyzed by a PS-supported pyrrolidine
-
Alza E, Cambeiro XC, Jimeno C, Pericàs MA. Highly enantioselective Michael additions in water catalyzed by a PS-supported pyrrolidine. Org Lett 2007;9:3717-3720.
-
(2007)
Org Lett
, vol.9
, pp. 3717-3720
-
-
Alza, E.1
Cambeiro, X.C.2
Jimeno, C.3
Pericàs, M.A.4
|