-
1
-
-
0034654216
-
Proline-Catalyzed Direct Asymmetric Aldol Reactions
-
List, B.; Lerner, R. A.; Barbas, C. F. Proline-Catalyzed Direct Asymmetric Aldol Reactions. J. Am. Chem. Soc. 2000, 122, 2395-2396.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2395-2396
-
-
List, B.1
Lerner, R.A.2
Barbas, C.F.3
-
2
-
-
0034596299
-
Catalytic Asymmetric Synthesis of anti-1,2-Diols
-
Notz, W.; List, B. Catalytic Asymmetric Synthesis of anti-1,2-Diols. J. Am. Chem. Soc. 2000, 122, 7386-7387.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7386-7387
-
-
Notz, W.1
List, B.2
-
3
-
-
0034600250
-
New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction
-
Ahrendt, K. A.; Borths, C. J.; MacMillan, D. W. C. New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels-Alder Reaction. J. Am. Chem. Soc. 2000, 122, 4243-4244.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4243-4244
-
-
Ahrendt, K.A.1
Borths, C.J.2
Macmillan, D.W.C.3
-
4
-
-
0003554758
-
Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries
-
Sigman, M. S.; Jacobsen, E. N. Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries. J. Am. Chem. Soc. 1998, 120, 4901-4902.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 4901-4902
-
-
Sigman, M.S.1
Jacobsen, E.N.2
-
5
-
-
0036927410
-
Direct Organocatalytic Aldol Reactions In. Buffered Aqueous Media
-
Córdova, A., Notz, W.; Barbas III, C. F. Direct organocatalytic aldol reactions in buffered aqueous media. Chem. Commun. 2002, 3024-3025.
-
(2002)
Chem. Commun.
, pp. 3024-3025
-
-
Córdova, A.1
Notz, W.2
Barbas III, C.F.3
-
6
-
-
0037012379
-
Aqueous Aldol Catalysis by a Nicotine Metabolite
-
Dickerson, T. J.; Janda, K. D. Aqueous Aldol Catalysis by a Nicotine Metabolite. J. Am. Chem. Soc. 2002, 124, 3220-3221.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3220-3221
-
-
Dickerson, T.J.1
Janda, K.D.2
-
7
-
-
28944449583
-
Effect of additives on the proline-catalyzed ketone-aldehyde aldol reactions
-
Pihko, P. M.; Laurikainen, K. M.; Usano, A.; Nyberg, A. I.; Kaavi, J. A. Effect of additives on the proline-catalyzed ketone-aldehyde aldol reactions. Tetrahedron 2006, 62, 317-328.
-
(2006)
Tetrahedron
, vol.62
, pp. 317-328
-
-
Pihko, P.M.1
Laurikainen, K.M.2
Usano, A.3
Nyberg, A.I.4
Kaavi, J.A.5
-
8
-
-
70449345895
-
Organocatalytic Reactions In Water
-
Raj, M.; Singh, V. K., Organocatalytic reactions in water. Chem. Commun. 2009, 6687-6703.
-
(2009)
Chem. Commun.
, pp. 6687-6703
-
-
Raj, M.1
Singh, V.K.2
-
9
-
-
58549093369
-
Water in Stereoselective Organocatalytic Reactions
-
Gruttadauria, M.; Giacalone, F.; Noto, R. Water in Stereoselective Organocatalytic Reactions. Adv. Synth. Catal. 2009, 351, 33-57.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 33-57
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
10
-
-
47749143706
-
Catalytic asymmetric aldol reactions in aqueous media
-
Mlynarski, J.; Paradowska, J. Catalytic asymmetric aldol reactions in aqueous media. Chem. Soc. Rev. 2008, 37, 1502-1511.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1502-1511
-
-
Mlynarski, J.1
Paradowska, J.2
-
11
-
-
77958060431
-
Water: Nature's Reaction Enforcer-Comparative Effects for Organic Synthesis "In-Water: And "On-Water
-
Butler, R.; Coyne, A. G. Water: Nature's Reaction Enforcer-Comparative Effects for Organic Synthesis In-Water: and "On-Water". Chem. Rev. 2010, 110, 6302-6337.
-
(2010)
Chem. Rev.
, vol.110
, pp. 6302-6337
-
-
Butler, R.1
Coyne, A.G.2
-
12
-
-
77955953727
-
In water, on water, and by water: Mimicking nature's aldolases with organocatalysis and water
-
Mase, M.; Barbas III, C.F. In water, on water, and by water: mimicking nature's aldolases with organocatalysis and water. Org. Biomol. Chem., 2010, 8, 4043-4050.
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 4043-4050
-
-
Mase, M.1
Barbas III, C.F.2
-
13
-
-
31444456557
-
Organocatalytic Direct Asymmetric Aldol Reactions in Water
-
Mase, N.; Nakai, Y.; Ohara, N.; Yoda, H.; Takabe, K.; Tanaka, F.; Barbas, C. F. Organocatalytic Direct Asymmetric Aldol Reactions in Water. J. Am. Chem. Soc. 2005, 128, 734-735.
-
(2005)
J. Am. Chem. Soc.
, vol.128
, pp. 734-735
-
-
Mase, N.1
Nakai, Y.2
Ohara, N.3
Yoda, H.4
Takabe, K.5
Tanaka, F.6
Barbas, C.F.7
-
14
-
-
32044463187
-
Highly Diastereo- and Enantioselective Direct Aldol Reactions in Water
-
Hayashi, Y.; Sumiya, T.; Takahashi, J.; Gotoh, H.; Urushima, T.; Shoji, M. Highly Diastereo- and Enantioselective Direct Aldol Reactions in Water. Angew. Chem. Int. Ed. 2006, 45, 958-961.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 958-961
-
-
Hayashi, Y.1
Sumiya, T.2
Takahashi, J.3
Gotoh, H.4
Urushima, T.5
Shoji, M.6
-
15
-
-
33748655418
-
Combined Proline-Surfactant Organocatalyst for the Highly Diastereo- and Enantioselective Aqueous Direct Cross-Aldol Reaction of Aldehydes
-
Hayashi, Y.; Aratake, S.; Okano, T.; Takahashi, J.; Sumiya, T.; Shoji, M. Combined Proline-Surfactant Organocatalyst for the Highly Diastereo- and Enantioselective Aqueous Direct Cross-Aldol Reaction of Aldehydes. Angew. Chem. Int. Ed. 2006, 45, 5527-5529.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5527-5529
-
-
Hayashi, Y.1
Aratake, S.2
Okano, T.3
Takahashi, J.4
Sumiya, T.5
Shoji, M.6
-
16
-
-
33748926253
-
Highly Enantioselective Direct Aldol Reaction Catalyzed by Organic Molecules
-
Raj, M., Vishnumaya; Ginotra, S. K.; Singh, V. K. Highly Enantioselective Direct Aldol Reaction Catalyzed by Organic Molecules. Org. Lett. 2006, 8, 4097-4099.
-
(2006)
Org. Lett.
, vol.8
, pp. 4097-4099
-
-
Raj, M.1
-
17
-
-
66249084153
-
Highly Efficient Small Organic Molecules for Enantioselective Direct Aldol Reaction in Organic and Aqueous Media
-
Vishnumaya, M. R.; Singh, V. K. Highly Efficient Small Organic Molecules for Enantioselective Direct Aldol Reaction in Organic and Aqueous Media. J. Org. Chem. 2009, 74, 4289-4297.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4289-4297
-
-
Vishnumaya, M.R.1
Singh, V.K.2
-
18
-
-
56749102623
-
Highly Enantioselective Organocatalyzed Construction of Quaternary Carbon Centers via Cross- Aldol Reaction of Ketones in Water
-
Zheng, C.; Wu, Y.; Wang, X.; Zhao, G. Highly Enantioselective Organocatalyzed Construction of Quaternary Carbon Centers via Cross- Aldol Reaction of Ketones in Water. Adv. Synth. Catal. 2008, 350, 2690-2694.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2690-2694
-
-
Zheng, C.1
Wu, Y.2
Wang, X.3
Zhao, G.4
-
19
-
-
34250700023
-
Organocatalytic asymmetric aldol reaction in the presence of water
-
Gryko, D.; Saletra, W. J. Organocatalytic asymmetric aldol reaction in the presence of water. Org. Biomol. Chem. 2007, 5, 2148-2153.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 2148-2153
-
-
Gryko, D.1
Saletra, W.J.2
-
20
-
-
49549107813
-
Highly Enantioselective Aldol Reactions Catalyzed by a Recyclable Fluorous (S) Pyrrolidine Sulfonamide on Water
-
Zu, L.; Xie, H.; Li, H.; Wang, J.; Wang, W. Highly Enantioselective Aldol Reactions Catalyzed by a Recyclable Fluorous (S) Pyrrolidine Sulfonamide on Water. Org. Lett. 2008, 10, 1211-1214.
-
(2008)
Org. Lett.
, vol.10
, pp. 1211-1214
-
-
Zu, L.1
Xie, H.2
Li, H.3
Wang, J.4
Wang, W.5
-
21
-
-
34547236177
-
Highly Efficient Threonine-Derived Organocatalysts for Direct Asymmetric Aldol Reactions in Water
-
Wu, X.; Jiang, Z.; Shen, H.-M.; Lu, Y. Highly Efficient Threonine-Derived Organocatalysts for Direct Asymmetric Aldol Reactions in Water. Adv. Synth. Catal. 2007, 349, 812-816.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 812-816
-
-
Wu, X.1
Jiang, Z.2
Shen, H.-M.3
Lu, Y.4
-
22
-
-
34250624385
-
Direct asymmetric aldol reactions catalyzed by a siloxy serine organocatalyst in water
-
Teo, Y.-C. Direct asymmetric aldol reactions catalyzed by a siloxy serine organocatalyst in water. Tetrahedron: Asymmetry 2007, 18, 1155-1158.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 1155-1158
-
-
Teo, Y.C.1
-
23
-
-
68749100830
-
Organic Solvent-Free Direct Asymmetric Aldol Reactions Catalyzed by a Siloxy Serine Organocatalyst in Brine
-
Teo, Y.-C.; Lee, P. P.-F. Organic Solvent-Free Direct Asymmetric Aldol Reactions Catalyzed by a Siloxy Serine Organocatalyst in Brine. Synth. Commun. 2009, 39, 3081 - 3091.
-
(2009)
Synth. Commun.
, vol.39
, pp. 3081-3091
-
-
Teo, Y.C.1
Lee P., P.F.2
-
24
-
-
66149105445
-
Water versus Solvent-Free Conditions for the Enantioselective Inter- and Intramolecular Aldol Reaction Employing L-Prolinamides and L-Prolinethioamides as Organocatalysts
-
Almasi, D.; Alonso, Diego A.; Balaguer, A.-N.; Nájera, C. Water versus Solvent-Free Conditions for the Enantioselective Inter- and Intramolecular Aldol Reaction Employing L-Prolinamides and L-Prolinethioamides as Organocatalysts. Adv. Synth. Catal. 2009, 351, 1123-1131.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 1123-1131
-
-
Almasi, D.1
Alonso Diego, A.2
Balaguer, A.N.3
Nájera, C.4
-
25
-
-
72149126893
-
Highly diastereo- and enantioselective direct aldol reactions by 4-tert-butyldimethylsiloxysubstituted organocatalysts derived from N-prolylsulfonamides in water
-
Fu, S.-d.; Fu, X.-k.; Zhang, S.-p.; Zou, X.-c.; Wu, X.-j. Highly diastereo- and enantioselective direct aldol reactions by 4-tert-butyldimethylsiloxysubstituted organocatalysts derived from N-prolylsulfonamides in water. Tetrahedron: Asymmetry 2009, 20, 2390-2396.
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 2390-2396
-
-
Fu, S.D.1
Fu, X.K.2
Zhang, S.-P.3
Zou, X.C.4
Wu, X.J.5
-
26
-
-
67649831572
-
Highly efficient primary amine organocatalysts for the direct asymmetric aldol reaction in brine
-
Ma, X.; Da, C.-S.; Yi, L.; Jia, Y.-N.; Guo, Q.-P.; Che, L.-P.; Wu, F.-C.; Wang, J.-R.; Li, W.-P. Highly efficient primary amine organocatalysts for the direct asymmetric aldol reaction in brine. Tetrahedron: Asymmetry 2009, 20, 1419-1424.
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1419-1424
-
-
Ma, X.1
Da, C.S.2
Yi, L.3
Jia, Y.N.4
Guo, Q.P.5
Che, L.P.6
Wu, F.C.7
Wang, J.R.8
Li, W.P.9
-
27
-
-
73149113747
-
Proline-β3-Amino-Ester Dipeptides as Efficient Catalysts for Enantioselective Direct Aldol Reaction in Aqueous Medium
-
De Nisco, M.; Pedatella, S.; Ullah, H.; Zaidi, J. H.; Naviglio, D.; Ozdamar, O. z. r.; Caputo, R. Proline-β3-Amino-Ester Dipeptides as Efficient Catalysts for Enantioselective Direct Aldol Reaction in Aqueous Medium. J. Org. Chem. 2009, 74, 9562-9565.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 9562-9565
-
-
de Nisco, M.1
Pedatella, S.2
Ullah, H.3
Zaidi, J.H.4
Naviglio, D.5
Ozdamar, O.Z.R.6
Caputo, R.7
-
28
-
-
38349023020
-
A novel (S)-proline-modified task-specific chiral ionic liquid--an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water
-
Siyutkin, D. E.; Kucherenko, A. S.; Struchkova, M. I.; Zlotin, S. G. A novel (S)-proline-modified task-specific chiral ionic liquid--an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water. Tetrahedron Letters 2008, 49, 1212-1216.
-
(2008)
Tetrahedron Letters
, vol.49
, pp. 1212-1216
-
-
Siyutkin, D.E.1
Kucherenko, A.S.2
Struchkova, M.I.3
Zlotin, S.G.4
-
29
-
-
71049188136
-
A new (S)-prolinamide modified by an ionic liquid moiety--a high performance recoverable catalyst for asymmetric aldol reactions in aqueous media
-
Siyutkin, D. E.; Kucherenko, A. S.; Zlotin, S. G. A new (S)-prolinamide modified by an ionic liquid moiety--a high performance recoverable catalyst for asymmetric aldol reactions in aqueous media. Tetrahedron 2010, 66, 513-518.
-
(2010)
Tetrahedron
, vol.66
, pp. 513-518
-
-
Siyutkin, D.E.1
Kucherenko, A.S.2
Zlotin, S.G.3
-
30
-
-
58149352252
-
Hydroxy-[alpha]-amino acids modified by ionic liquid moieties: Recoverable organocatalysts for asymmetric aldol reactions in the presence of water
-
Siyutkin, D. E.; Kucherenko, A. S.; Zlotin, S. G. Hydroxy-[alpha]-amino acids modified by ionic liquid moieties: recoverable organocatalysts for asymmetric aldol reactions in the presence of water. Tetrahedron 2009, 65, 1366-1372.
-
(2009)
Tetrahedron
, vol.65
, pp. 1366-1372
-
-
Siyutkin, D.E.1
Kucherenko, A.S.2
Zlotin, S.G.3
-
31
-
-
55549129267
-
modular approach to catalyst hydrophobicity for an asymmetric aldol reaction in a biphasic aqueous environment
-
Lombardo, M.; Easwar, S.; Marco, A. D.; Pasi, F.; Trombini, C. A modular approach to catalyst hydrophobicity for an asymmetric aldol reaction in a biphasic aqueous environment. Org. Biomol. Chem. 2008, 6, 4224-4229.
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 4224-4229
-
-
Lombardo, M.1
Easwar, S.2
Marco, A.D.3
Pasi, F.4
Trombini, C.A.5
-
32
-
-
54149117629
-
Direct Asymmetric Aldol Reaction Catalyzed by an Imidazolium-Tagged trans-4- Hydroxy-l-proline under Aqueous Biphasic Conditions
-
Lombardo, M.; Pasi, F.; Easwar, S.; Trombini, C. Direct Asymmetric Aldol Reaction Catalyzed by an Imidazolium-Tagged trans-4- Hydroxy-l-proline under Aqueous Biphasic Conditions. Synlett 2008, 2008, 2471-2474.
-
(2008)
Synlett
, vol.2008
, pp. 2471-2474
-
-
Lombardo, M.1
Pasi, F.2
Easwar, S.3
Trombini, C.4
-
33
-
-
58549103519
-
The Ion Tag Strategy as a Route to Highly Efficient Organocatalysts for the Direct Asymmetric Aldol Reaction
-
Lombardo, M.; Easwar, S.; Pasi, F.; Trombini, C. The Ion Tag Strategy as a Route to Highly Efficient Organocatalysts for the Direct Asymmetric Aldol Reaction. Adv. Synth. Catal. 2009, 351, 276-282.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 276-282
-
-
Lombardo, M.1
Easwar, S.2
Pasi, F.3
Trombini, C.4
-
34
-
-
69149083759
-
The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water
-
Chimni, S. S.; Singh, S.; Kumar, A. The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water. Tetrahedron: Asymmetry 2009, 20, 1722-1724.
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1722-1724
-
-
Chimni, S.S.1
Singh, S.2
Kumar, A.3
-
35
-
-
0037420807
-
Proline catalyzed aldol reactions in aqueous micelles: An environmentally friendly reaction system
-
Peng, Y.-Y.; Ding, Q.-P.; Li, Z.; Wang, P. G.; Cheng, J.-P. Proline catalyzed aldol reactions in aqueous micelles: an environmentally friendly reaction system. Tetrahedron Lett. 2003, 44, 3871-3875.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3871-3875
-
-
Peng, Y.Y.1
Ding, Q.-P.2
Li, Z.3
Wang, P.G.4
Cheng, J.-P.5
-
36
-
-
72149095111
-
Effect of Long Chain Fatty Acids on Organocatalytic Aqueous Direct Aldol Reactions
-
Mase, N.; Noshiro, N.; Mokuya, A.; Takabe, K. Effect of Long Chain Fatty Acids on Organocatalytic Aqueous Direct Aldol Reactions. Adv. Synth. Catal. 2009, 351, 2791-2796.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 2791-2796
-
-
Mase, N.1
Noshiro, N.2
Mokuya, A.3
Takabe, K.4
-
37
-
-
56749154215
-
New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium
-
Giacalone, F.; Gruttadauria, M.; Meo, P. L.; Riela, S.; Noto, R. New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium. Adv. Synth. Catal. 2008, 350, 2747-2760.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2747-2760
-
-
Giacalone, F.1
Gruttadauria, M.2
Meo, P.L.3
Riela, S.4
Noto, R.5
-
38
-
-
70450177301
-
Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water
-
Gruttadauria, M.; Salvo, A. M. P.; Giacalone, F.; Agrigento, P.; Noto, R. Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water. Eur. J. Org. Chem. 2009, 2009, 5437-5444.
-
(2009)
Eur. J. Org. Chem.
, vol.2009
, pp. 5437-5444
-
-
Gruttadauria, M.1
Salvo, A.M.P.2
Giacalone, F.3
Agrigento, P.4
Noto, R.5
-
39
-
-
53849141478
-
Novel Prolinamide-Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction
-
Gruttadauria, M.; Giacalone, F.; Marculescu, A. M.; Noto, R. Novel Prolinamide-Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction. Adv. Synth. Catal. 2008, 350, 1397-1405.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1397-1405
-
-
Gruttadauria, M.1
Giacalone, F.2
Marculescu, A.M.3
Noto, R.4
-
40
-
-
33845336873
-
Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and [alpha]-selenenylation of aldehydes
-
Giacalone, F.; Gruttadauria, M.; Marculescu, A. M.; Noto, R. Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and [alpha]-selenenylation of aldehydes. Tetrahedron Lett. 2007, 48, 255-259.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 255-259
-
-
Giacalone, F.1
Gruttadauria, M.2
Marculescu, A.M.3
Noto, R.4
-
41
-
-
33750070045
-
Polystyrene-Supported Hydroxyproline: An Insoluble, Recyclable Organocatalyst for the Asymmetric Aldol Reaction in Water
-
Font, D.; Jimeno, C.; Pericas, M. A. Polystyrene-Supported Hydroxyproline: An Insoluble, Recyclable Organocatalyst for the Asymmetric Aldol Reaction in Water. Org. Lett. 2006, 8, 4653-4655.
-
(2006)
Org. Lett.
, vol.8
, pp. 4653-4655
-
-
Font, D.1
Jimeno, C.2
Pericas, M.A.3
-
42
-
-
27144559611
-
Direct asymmetric aldol reaction in aqueous media using polymer-supported peptide
-
Akagawa, K.; Sakamoto, S.; Kudo, K. Direct asymmetric aldol reaction in aqueous media using polymer-supported peptide. Tetrahedron Lett. 2005, 46, 8185-8187.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8185-8187
-
-
Akagawa, K.1
Sakamoto, S.2
Kudo, K.3
-
43
-
-
67650333080
-
Synthesis of Acrylic Polymer Beads for Solid-Supported Proline-Derived Organocatalysts
-
Kristensen, T. E.; Vestli, K.; Fredriksen, K. A.; Hansen, F. K.; Hansen, T. Synthesis of Acrylic Polymer Beads for Solid-Supported Proline-Derived Organocatalysts. Org. Lett. 2009, 11, 2968-2971.
-
(2009)
Org. Lett.
, vol.11
, pp. 2968-2971
-
-
Kristensen, T.E.1
Vestli, K.2
Fredriksen, K.A.3
Hansen, F.K.4
Hansen, T.5
-
44
-
-
69449097485
-
Highly Enantioselective Direct Aldol Reactions Catalyzed by Proline Derivatives Based on a Calix[4]arene Scaffold in the Presence of Water
-
Li, Z.-Y.; Chen, J.-W.; Wang, L.; Pan, Y. Highly Enantioselective Direct Aldol Reactions Catalyzed by Proline Derivatives Based on a Calix[4]arene Scaffold in the Presence of Water. Synlett 2009, 2009, 2356-2360.
-
(2009)
Synlett
, vol.2009
, pp. 2356-2360
-
-
Li, Z.-Y.1
Chen, J.-W.2
Wang, L.3
Pan, Y.4
-
45
-
-
33750041086
-
Highly Efficient and Reusable Dendritic Catalysts Derived from N-Prolylsulfonamide for the Asymmetric Direct Aldol Reaction in Water
-
Wu, Y.; Zhang, Y.; Yu, M.; Zhao, G.; Wang, S. Highly Efficient and Reusable Dendritic Catalysts Derived from N-Prolylsulfonamide for the Asymmetric Direct Aldol Reaction in Water. Org. Lett. 2006, 8, 4417-4420.
-
(2006)
Org. Lett.
, vol.8
, pp. 4417-4420
-
-
Wu, Y.1
Zhang, Y.2
Yu, M.3
Zhao, G.4
Wang, S.5
-
46
-
-
68049101360
-
Structural Effects on the Catalytic, Emulsifying, and Recycling Properties of Chiral Amphiphilic Dendritic Organocatalysts
-
Lo, C.-M.; Chow, H.-F. Structural Effects on the Catalytic, Emulsifying, and Recycling Properties of Chiral Amphiphilic Dendritic Organocatalysts. J. Org. Chem. 2009, 74, 5181-5191.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5181-5191
-
-
Lo, C.-M.1
Chow, H.-F.2
-
47
-
-
77953130840
-
Simple amphiphilic isosteviol-proline conjugate as chiral catalysts for the direct asymmetric aldol reaction in the presence of water
-
An, Y.-J.; Zhang, Y.-X.; Wu, Y.; Liu, Z.-M.; Pi,C.; Tao J.-C. Simple amphiphilic isosteviol-proline conjugate as chiral catalysts for the direct asymmetric aldol reaction in the presence of water. Tetrahedron: Asymmetry 2010, 21, 688-694.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 688-694
-
-
An, Y.-J.1
Zhang, Y.-X.2
Wu, Y.3
Liu, Z.-M.4
Pi, C.5
Tao, J.-C.6
-
48
-
-
78249281374
-
Advances towards Highly Active and Stereoselective Simple and Cheap Proline-Based Organocatalysts
-
Giacalne, F.; Gruttadauria, M.; Agrigento P.; Lo Melo, P.; Noto, R. Advances towards Highly Active and Stereoselective Simple and Cheap Proline-Based Organocatalysts. Eur. J. Org. Chem. 2010, 5696-5704.
-
(2010)
Eur. J. Org. Chem.
, pp. 5696-5704
-
-
Giacalne, F.1
Gruttadauria, M.2
Agrigento, P.3
Lo Melo, P.4
Noto, R.5
-
49
-
-
78349270190
-
Highly Efficient Direct Asymmetric Aldol Reactions Catalyzed by a Prolinethioamide Derivative in Aqueous Media
-
Wang, B.; Liu X.-W.; Liu, L.-Y; Chang, W. X.; Li, J., Highly Efficient Direct Asymmetric Aldol Reactions Catalyzed by a Prolinethioamide Derivative in Aqueous Media. Eur. J. Org. Chem. 2010, 5951-5954.
-
(2010)
Eur. J. Org. Chem.
, pp. 5951-5954
-
-
Wang, B.1
Liu, X.-W.2
Liu, L.-Y.3
Chang, W.X.4
Li, J.5
-
50
-
-
77950233672
-
Direct Asymmetric Aldol Reaction with Recyclale Fluorous Organocatalyst
-
Miura, T.; Imai, K.; Ina, M.; Tada, N.; Imai, N.; Itoh A. Direct Asymmetric Aldol Reaction with Recyclale Fluorous Organocatalyst. Org. Lett. 2010, 12, 1620-1623.
-
(2010)
Org. Lett.
, vol.12
, pp. 1620-1623
-
-
Miura, T.1
Imai, K.2
Ina, M.3
Tada, N.4
Imai, N.5
Itoh, A.6
-
51
-
-
78649874385
-
Direct asymmetric aldol reaction cocatalyzed by L-proline and 12 elements Lewis acids in the presence of water
-
Penjoat, M.; Barbry D.; Rolando C. Direct asymmetric aldol reaction cocatalyzed by L-proline and 12 elements Lewis acids in the presence of water. Tetrahedron Lett. 2011, 52, 159-162.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 159-162
-
-
Penjoat, M.1
Barbry, D.2
Rolando, C.3
-
52
-
-
34547198987
-
Organocatalytic enantioselective Michael and hetero-Michael reactions
-
Vicario, J. L.; Badia, D.; Carrillo, L., Organocatalytic enantioselective Michael and hetero-Michael reactions. Synthesis 2007, 2065-2092.
-
(2007)
Synthesis
, pp. 2065-2092
-
-
Vicario, J.L.1
Badia, D.2
Carrillo, L.3
-
53
-
-
34547463692
-
Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation
-
Sulzer- Mosse, S.; Alexakis, A. Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation. Chem. Commun. 2007, 3123-3135.
-
(2007)
Chem. Commun.
, pp. 3123-3135
-
-
Sulzer-, M.S.1
Alexakis, A.2
-
54
-
-
34250613134
-
Recent Advances in Asymmetric Organocatalytic 1,4-Conjugate Additions
-
Tsogoeva, S. B. Recent Advances in Asymmetric Organocatalytic 1,4-Conjugate Additions. Eur. J. Org. Chem. 2007, 1701-1716.
-
(2007)
Eur. J. Org. Chem.
, pp. 1701-1716
-
-
Tsogoeva, S.B.1
-
55
-
-
33847623075
-
Organocatalytic asymmetric conjugate additions
-
Almasi, D.; Alonso, D. A.; Nájera, C. Organocatalytic asymmetric conjugate additions. Tetrahedron: Asymmetry 2007, 18, 299-365.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 299-365
-
-
Almasi, D.1
Alonso, D.A.2
Nájera, C.3
-
56
-
-
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, C. F. 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
-
57
-
-
34848859862
-
Highly Enantioselective Michael Additions in Water Catalyzed by a PS-Supported Pyrrolidine
-
Alza, E.; Cambeiro, X. C.; Jimeno, C.; Pericàs, M. A. 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
-
58
-
-
33746620447
-
Recyclable Fluorous (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 Fluorous (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.A.4
-
59
-
-
33748152821
-
Surfactant-type asymmetric organocatalyst: Organocatalytic asymmetric Michael addition to nitrostyrenes in water
-
Luo, S.; Mi, X.; Liu, S.; Xu, H.; Cheng, J.-P. Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water. Chem. Commun. 2006, 3687-3689.
-
(2006)
Chem. Commun.
, pp. 3687-3689
-
-
Luo, S.1
Mi, X.2
Liu, S.3
Xu, H.4
Cheng, J.-P.5
-
60
-
-
33751407719
-
Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts
-
Cao, Y.-J.; Lai, Y.-Y.; Wang, X.; Li, Y.-J.; Xiao, W.-J. Michael additions in water of ketones to nitroolefins catalyzed by readily tunable and bifunctional pyrrolidine-thiourea organocatalysts. Tetrahedron Lett. 2007, 48, 21-24.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 21-24
-
-
Cao, Y.-J.1
Lai, Y.-Y.2
Wang, X.3
Li, Y.-J.4
Xiao, W.-J.5
-
61
-
-
65449174801
-
Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether
-
Chuan, Y.; Chen, G.; Peng, Y. Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether. Tetrahedron Lett. 2009, 50, 3054-3058.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 3054-3058
-
-
Chuan, Y.1
Chen, G.2
Peng, Y.3
-
62
-
-
47049110777
-
Silicasupported pyrrolidine-triazole, an insoluble, recyclable organocatalyst for the enantioselective Michael addition of ketones to nitroalkenes
-
Zhao, Y.-B.; Zhang, L.-W.; Wu, L.-Y.; Zhong, X.; Li, R.; Ma, J.-T. Silicasupported pyrrolidine-triazole, an insoluble, recyclable organocatalyst for the enantioselective Michael addition of ketones to nitroalkenes. Tetrahedron: Asymmetry 2008, 19, 1352-1355.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 1352-1355
-
-
Zhao, Y.-B.1
Zhang, L.-W.2
Wu, L.-Y.3
Zhong, X.4
Li, R.5
Ma, J.-T.6
-
63
-
-
38949133131
-
Highly Efficient Catalytic System for Enantioselective Michael Addition of Aldehydes to Nitroalkenes in Water
-
Zhu, S.; Yu, S.; Ma, D. Highly Efficient Catalytic System for Enantioselective Michael Addition of Aldehydes to Nitroalkenes in Water. Angew. Chem. Int. Ed. 2008, 47, 545-548.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 545-548
-
-
Zhu, S.1
Yu, S.2
Ma, D.3
-
64
-
-
41649092639
-
Enantioselective organocatalytic Michael addition of malonates to [alpha],[beta]-unsaturated aldehydes in water
-
Ma, A.; Zhu, S.; Ma, D. Enantioselective organocatalytic Michael addition of malonates to [alpha],[beta]-unsaturated aldehydes in water. Tetrahedron Letters 2008, 49, 3075-3077.
-
(2008)
Tetrahedron Letters
, vol.49
, pp. 3075-3077
-
-
Ma, A.1
Zhu, S.2
Ma, D.3
-
65
-
-
48849084149
-
Enantioselective Assembly of Substituted Dihydropyrones via Organocatalytic Reaction in Water Media
-
Wang, J.; Yu, F.; Zhang, X.; Ma, D. Enantioselective Assembly of Substituted Dihydropyrones via Organocatalytic Reaction in Water Media. Org. Lett. 2008, 10, 2561-2564.
-
(2008)
Org. Lett.
, vol.10
, pp. 2561-2564
-
-
Wang, J.1
Yu, F.2
Zhang, X.3
Ma, D.4
-
66
-
-
68149110229
-
Di(methylimidazole)prolinol Silyl Ether Catalyzed Highly Michael Addition of Aldehydes to Nitroolefins in Water
-
Wu, J.; Ni, B.; Headley, A. D. Di(methylimidazole)prolinol Silyl Ether Catalyzed Highly Michael Addition of Aldehydes to Nitroolefins in Water. Org. Lett. 2009, 11, 3354-3356.
-
(2009)
Org. Lett.
, vol.11
, pp. 3354-3356
-
-
Wu, J.1
Ni, B.2
Headley, A.D.3
-
67
-
-
72149085433
-
Highly Efficient Ion-Tagged Catalyst for the Enantioselective Michael Addition of Aldehydes to Nitroalkenes
-
Lombardo, M.; Chiarucci, M.; Quintavalla, A.; Trombini, C. Highly Efficient Ion-Tagged Catalyst for the Enantioselective Michael Addition of Aldehydes to Nitroalkenes. Adv. Synth. Catal. 2009, 351, 2801-2806.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 2801-2806
-
-
Lombardo, M.1
Chiarucci, M.2
Quintavalla, A.3
Trombini, C.4
-
68
-
-
72149122415
-
A new type of organocatalyst for highly stereoselective Michael addition of ketones to nitroolefins on water
-
Syu, S.-E.; Kao, T.-T.; Lin, W. A new type of organocatalyst for highly stereoselective Michael addition of ketones to nitroolefins on water. Tetrahedron 2010, 66, 891-897.
-
(2010)
Tetrahedron
, vol.66
, pp. 891-897
-
-
Syu, S.-E.1
Kao, T.-T.2
Lin, W.3
-
69
-
-
74849103683
-
Diarylprolinol Silyl Ether Salts as New, Efficient, Water-Soluble, and Recyclable Organocatalysts for the Asymmetric Michael Addition on Water
-
Zheng, Z.; Perkins, B. L.; Ni, B. Diarylprolinol Silyl Ether Salts as New, Efficient, Water-Soluble, and Recyclable Organocatalysts for the Asymmetric Michael Addition on Water. J. Am. Chem. Soc. 2009, 132, 50-51.
-
(2009)
J. Am. Chem. Soc.
, vol.132
, pp. 50-51
-
-
Zheng, Z.1
Perkins, B.L.2
Ni, B.3
-
70
-
-
57549115024
-
A Highly Efficient and Recyclable Ionic Liquid Anchored Pyrrolidine Catalyst for Enantioselective Michael Additions
-
Miao, T.; Wang, L.; Li, P.; Yan, J. A Highly Efficient and Recyclable Ionic Liquid Anchored Pyrrolidine Catalyst for Enantioselective Michael Additions. Synthesis 2008, 2008, 3828-3834.
-
(2008)
Synthesis
, vol.2008
, pp. 3828-3834
-
-
Miao, T.1
Wang, L.2
Li, P.3
Yan, J.4
-
71
-
-
34748882366
-
Ionic-liquidsupported organocatalyst for the enantioselective Michael addition of ketones to nitroolefins
-
Wu, L.-Y.; Yan, Z.-Y.; Xie, Y.-X.; Niu, Y.-N.; Liang, Y.-M. Ionic-liquidsupported organocatalyst for the enantioselective Michael addition of ketones to nitroolefins. Tetrahedron: Asymmetry 2007, 18, 2086-2090.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2086-2090
-
-
Wu, L.-Y.1
Yan, Z.-Y.2
Xie, Y.-X.3
Niu, Y.-N.4
Liang, Y.-M.5
-
72
-
-
61349135678
-
Enantioselective Organocatalytic Conjugate Addition of Aldehydes to Nitrodienes
-
Belot, S.; Massaro, A.; Tenti, A.; Mordini, A.; Alexakis, A. Enantioselective Organocatalytic Conjugate Addition of Aldehydes to Nitrodienes. Org. Lett. 2008, 10, 4557-4560.
-
(2008)
Org. Lett.
, vol.10
, pp. 4557-4560
-
-
Belot, S.1
Massaro, A.2
Tenti, A.3
Mordini, A.4
Alexakis, A.5
-
73
-
-
36148957495
-
Water- Compatible Iminium Activation: Organocatalytic Michael Reactions of Carbon-Centered Nucleophiles with Enals
-
Palomo, C.; Landa, A.; Mielgo, A.; Oiarbide, M.; Puente, Á.; Vera, S. Water- Compatible Iminium Activation: Organocatalytic Michael Reactions of Carbon-Centered Nucleophiles with Enals. Angew. Chem. Int. Ed. 2007, 46, 8431-8435.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 8431-8435
-
-
Palomo, C.1
Landa, A.2
Mielgo, A.3
Oiarbide, M.4
Puente, Á.5
Vera, S.6
-
74
-
-
53849122328
-
Enantioselective Michael Addition of Dicyanoolefins to alpha,beta-Unsaturated Aldehydes in Aqueous Medium
-
Lu, J.; Liu, F.; Loh, T.-P. Enantioselective Michael Addition of Dicyanoolefins to alpha,beta-Unsaturated Aldehydes in Aqueous Medium. Adv. Synth. Catal. 2008, 350, 1781-1784.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1781-1784
-
-
Lu, J.1
Liu, F.2
Loh, T.-P.3
-
75
-
-
70350150903
-
O-TMS-alpha,alphadiphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between alpha,beta- Enals and Dialkyl Malonates
-
Maltsev, O. V.; Kucherenko, A. S.; Zlotin, S. G. O-TMS-alpha,alphadiphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between alpha,beta- Enals and Dialkyl Malonates. Eur. J. Org. Chem. 2009, 2009, 5134-5137.
-
(2009)
Eur. J. Org. Chem.
, vol.2009
, pp. 5134-5137
-
-
Maltsev, O.V.1
Kucherenko, A.S.2
Zlotin, S.G.3
-
76
-
-
77956338488
-
Functionalized proline with double hydrogen bonding potential: Highly enantioselective Michael adition of carbonyl compounds to β-nitrostyrenes in brine
-
Saha, S.; Seth, S.; Moorthy, J. N. Functionalized proline with double hydrogen bonding potential: highly enantioselective Michael adition of carbonyl compounds to β-nitrostyrenes in brine. Tetrahedron Lett. 2010, 51, 5281-5286.
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 5281-5286
-
-
Saha, S.1
Seth, S.2
Moorthy, J.N.3
-
77
-
-
78349262620
-
Highly Active Water-Soluble and Recyclable Organocatalyst for the Asymmetric 1,4-Conjugate Addition of Nitroalkanes to α,β-Unsaturated Aldehydes
-
Ghosh, S. K.; Zheng, Z.; Ni, B. Highly Active Water-Soluble and Recyclable Organocatalyst for the Asymmetric 1,4-Conjugate Addition of Nitroalkanes to α,β-Unsaturated Aldehydes. Adv. Synth. Catal., 2010, 352, 2378-2382.
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2378-2382
-
-
Ghosh, S.K.1
Zheng, Z.2
Ni, B.3
-
78
-
-
77955384489
-
The Organocatalytic Enantioselective Michael Addition of Aldehydes to Vinyl Sulfones in Water
-
Xiao, J.; Liu, Y.-L.; Loh T.-P. The Organocatalytic Enantioselective Michael Addition of Aldehydes to Vinyl Sulfones in Water. Synlett, 2010, 2029-2032.
-
(2010)
Synlett
, pp. 2029-2032
-
-
Xiao, J.1
Liu, Y.-L.2
Loh, T.-P.3
-
79
-
-
78649877354
-
Organocatalytic Michael addition of aldehydes to a,β-silylmethylene malonate to form intermediates for the enantioselective synthesis of hydroxylated valerolactones and piperidines
-
Chowdhury, R.; Ghosh, S. K. Organocatalytic Michael addition of aldehydes to a,β-silylmethylene malonate to form intermediates for the enantioselective synthesis of hydroxylated valerolactones and piperidines. Tetrahedron: Asymmetry, 2010, 21, 2696-2702.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2696-2702
-
-
Chowdhury, R.1
Ghosh, S.K.2
-
80
-
-
38149118178
-
Organocatalysed asymmetric Mannich reactions
-
Verkade, J. M. M.; Hemert, L. J. C. V.; Quaedflieg, P. J. L. M.; Rutjes, F. P. J. T. Organocatalysed asymmetric Mannich reactions. Chem. Soc. Rev. 2008, 37, 29-41.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 29-41
-
-
Verkade, J.M.M.1
Hemert, L.J.C.V.2
Quaedflieg, P.J.L.M.3
Rutjes, F.P.J.T.4
-
81
-
-
37349005457
-
Organocatalytic Asymmetric Mannich Reactions: New Methodology, Catalyst Design, and Synthetic Applications
-
Ting, A.; Schaus, S. E. Organocatalytic Asymmetric Mannich Reactions: New Methodology, Catalyst Design, and Synthetic Applications. Eur. J. Org. Chem. 2007, 2007, 5797-5815.
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 5797-5815
-
-
Ting, A.1
Schaus, S.E.2
-
82
-
-
21244473265
-
Dihydroxyacetone in Amino Acid Catalyzed Mannich-Type Reactions
-
Westermann, B.; Neuhaus, C. Dihydroxyacetone in Amino Acid Catalyzed Mannich-Type Reactions. Angew. Chem. Int. Ed. 2005, 44, 4077-4079.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 4077-4079
-
-
Westermann, B.1
Neuhaus, C.2
-
83
-
-
38349145665
-
Organic Solvent- Free, Enantio- and Diastereoselective, Direct Mannich Reaction in the Presence of Water
-
Hayashi, Y.; Urushima, T.; Aratake, S.; Okano, T.; Obi, K. Organic Solvent- Free, Enantio- and Diastereoselective, Direct Mannich Reaction in the Presence of Water. Org. Lett. 2008, 10, 21-24.
-
(2008)
Org. Lett.
, vol.10
, pp. 21-24
-
-
Hayashi, Y.1
Urushima, T.2
Aratake, S.3
Okano, T.4
Obi, K.5
-
84
-
-
33846529045
-
Evidence of Asymmetric Autocatalysis in Organocatalytic Reactions
-
Mauksch, M.; Tsogoeva, Svetlana B.; Martynova, Irina M.; Wei, S. Evidence of Asymmetric Autocatalysis in Organocatalytic Reactions. Angew. Chem. Int. Ed. 2007, 46, 393-396.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 393-396
-
-
Mauksch, M.1
Tsogoeva Svetlana, B.2
Martynova, I.M.3
Wei, S.4
-
85
-
-
46149091526
-
Asymmetric autocatalytic Mannich reaction in the presence of water and its implication in prebiotic chemistry
-
Amedjkouh, M.; Brandberg, M. Asymmetric autocatalytic Mannich reaction in the presence of water and its implication in prebiotic chemistry. Chem. Commun. 2008, 3043-3045.
-
(2008)
Chem. Commun.
, pp. 3043-3045
-
-
Amedjkouh, M.1
Brandberg, M.2
-
86
-
-
38749144743
-
Direct asymmetric three-component Mannich reactions catalyzed by a siloxy serine organocatalyst in water
-
Teo, Y.-C.; Lau, J.-J.; Wu, M.-C. Direct asymmetric three-component Mannich reactions catalyzed by a siloxy serine organocatalyst in water. Tetrahedron: Asymmetry 2008, 19, 186-190.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 186-190
-
-
Teo, Y.-C.1
Lau, J.-J.2
Wu, M.-C.3
-
87
-
-
33947545143
-
Direct asymmetric three-component organocatalytic anti-selective Mannich reactions in a purely aqueous system
-
Cheng, L.; Wu, X.; Lu, Y. Direct asymmetric three-component organocatalytic anti-selective Mannich reactions in a purely aqueous system. Org. Biomol. Chem. 2007, 5, 1018-1020.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1018-1020
-
-
Cheng, L.1
Wu, X.2
Lu, Y.3
-
88
-
-
0037139610
-
The First General Enantioselective Catalytic Diels-Alder Reaction with Simple α,β- Unsaturated Ketones
-
Northrup, A. B.; MacMillan, D. W. C. The First General Enantioselective Catalytic Diels-Alder Reaction with Simple α,β- Unsaturated Ketones. J. Am. Chem. Soc. 2002, 124, 2458-2460.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2458-2460
-
-
Northrup, A.B.1
Macmillan, D.W.C.2
-
89
-
-
25444465184
-
Aqueous Enantioselective Organocatalytic Diels-Alder Reactions Employing Hydrazide Catalysts. A New Scaffold for Organic Acceleration
-
Lemay, M.; Ogilvie, W. W. Aqueous Enantioselective Organocatalytic Diels-Alder Reactions Employing Hydrazide Catalysts. A New Scaffold for Organic Acceleration. Org. Lett. 2005, 7, 4141-4144.
-
(2005)
Org. Lett.
, vol.7
, pp. 4141-4144
-
-
Lemay, M.1
Ogilvie, W.W.2
-
90
-
-
34547224498
-
Design of a Conformationally Rigid Hydrazide Organic Catalyst
-
Lemay, M.; Aumand, L.; Ogilvie, William W. Design of a Conformationally Rigid Hydrazide Organic Catalyst. Adv. Synth. Catal. 2007, 349, 441-447.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 441-447
-
-
Lemay, M.1
Aumand, L.2
Ogilvie3
William, W.4
-
91
-
-
33845701141
-
Aziridin-2-yl methanols as organocatalysts in Diels-Alder reactions and Friedel-Crafts alkylations of N-methyl-pyrrole and N-methylindole
-
Bonini, B. F.; Capitò, E.; Comes-Franchini, M.; Fochi, M.; Ricci, A.; Zwanenburg, B. Aziridin-2-yl methanols as organocatalysts in Diels-Alder reactions and Friedel-Crafts alkylations of N-methyl-pyrrole and N-methylindole. Tetrahedron: Asymmetry 2006, 17, 3135-3143.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3135-3143
-
-
Bonini, B.F.1
Capitò, E.2
Comes-Franchini, M.3
Fochi, M.4
Ricci, A.5
Zwanenburg, B.6
-
92
-
-
53249140774
-
Asymmetric Diels-Alder Reactions of alpha,beta-Unsaturated Aldehydes Catalyzed by a Diarylprolinol Silyl Ether Salt in the Presence of Water
-
Hayashi, Y.; Samanta, S.; Gotoh, H.; Ishikawa, H. Asymmetric Diels-Alder Reactions of alpha,beta-Unsaturated Aldehydes Catalyzed by a Diarylprolinol Silyl Ether Salt in the Presence of Water. Angew. Chem. Int. Ed. 2008, 47, 6634-6637.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6634-6637
-
-
Hayashi, Y.1
Samanta, S.2
Gotoh, H.3
Ishikawa, H.4
-
93
-
-
77951119729
-
2-symmetric bipyrrolidines: Catalyst recycling in water medium and insight into the catalytic mode
-
Ma, Y.; Jin, S.; Kan, Y.; Zhang, Y. J.; Zhang,W. Highly active asymmetric Diels-Alder reactions catalyzed by C2-symmetric bipyrrolidines: catalyst recycling in water medium and insight into the catalytic mode. Tetrahedron 2010, 66, 3849-3854.
-
(2010)
Tetrahedron
, vol.66
, pp. 3849-3854
-
-
Ma, Y.1
Jin, S.2
Kan, Y.3
Zhang, Y.J.4
Zhang, W.5
-
94
-
-
34250327977
-
Dual Reactivity Pattern of Allenolates ldquoOn Waterrdquo: The Chemical Basis for Efficient Allenolate-Driven Organocatalytic Systems
-
González-Cruz, D.; Tejedor, D.; de Armas, P.; García-Tellado, F. Dual Reactivity Pattern of Allenolates ldquoOn Waterrdquo: The Chemical Basis for Efficient Allenolate-Driven Organocatalytic Systems. Chem. Eur. J. 2007, 13, 4823-4832.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 4823-4832
-
-
González-Cruz, D.1
Tejedor, D.2
de Armas, P.3
García-Tellado, F.4
-
95
-
-
33846336715
-
Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalysts
-
Kumar, A.; Maurya, R. A. Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalysts. Tetrahedron 2007, 63, 1946-1952.
-
(2007)
Tetrahedron
, vol.63
, pp. 1946-1952
-
-
Kumar, A.1
Maurya, R.A.2
-
96
-
-
85197361263
-
Polarity-Directed One-Pot Asymmetric Cascade Reactions Mediated by Two Catalysts in an Aqueous Buffer
-
9999, NA
-
Scroggins, S. T.; Chi, Y.; Fréchet, J. M. J. Polarity-Directed One-Pot Asymmetric Cascade Reactions Mediated by Two Catalysts in an Aqueous Buffer. Angew. Chem. Int. Ed. 2009, 9999, NA.
-
(2009)
Angew. Chem. Int. Ed.
-
-
Scroggins, S.T.1
Chi, Y.2
Fréchet, J.M.J.3
-
97
-
-
48549088106
-
Reusable montmorillonite-entrapped organocatalyst for asymmetric Diels-Alder reaction
-
Mitsudome, T.; Nose, K.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Reusable montmorillonite-entrapped organocatalyst for asymmetric Diels-Alder reaction. Tetrahedron Lett. 2008, 49, 5464-5466.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 5464-5466
-
-
Mitsudome, T.1
Nose, K.2
Mizugaki, T.3
Jitsukawa, K.4
Kaneda, K.5
-
98
-
-
58549090627
-
Chiral Amine-Polyoxometalate Hybrids as Recoverable Asymmetric Enamine Catalysts under Neat and Aqueous Conditions
-
Li, J.; Hu, S.; Luo, S.; Cheng, J.-P. Chiral Amine-Polyoxometalate Hybrids as Recoverable Asymmetric Enamine Catalysts under Neat and Aqueous Conditions. Eur. J. Org. Chem. 2009, 2009, 132-140.
-
(2009)
Eur. J. Org. Chem.
, vol.2009
, pp. 132-140
-
-
Li, J.1
Hu, S.2
Luo, S.3
Cheng, J.-P.4
-
99
-
-
73149097919
-
Nano-organocatalyst: Magnetically retrievable ferrite-anchored glutathione for microwave-assisted Paal-Knorr reaction, aza-Michael addition, and pyrazole synthesis
-
Polshettiwar, V.; Varma, R. S. Nano-organocatalyst: magnetically retrievable ferrite-anchored glutathione for microwave-assisted Paal-Knorr reaction, aza-Michael addition, and pyrazole synthesis. Tetrahedron 2010, 66, 1091-1097.
-
(2010)
Tetrahedron
, vol.66
, pp. 1091-1097
-
-
Polshettiwar, V.1
Varma, R.S.2
-
100
-
-
56349159222
-
Asymmetric bifunctional primary aminocatalysis on magnetic nanoparticles
-
Luo, S.; Zheng, X.; Cheng, J.-P. Asymmetric bifunctional primary aminocatalysis on magnetic nanoparticles. Chem. Commun. 2008, 5719-5721.
-
(2008)
Chem. Commun.
, pp. 5719-5721
-
-
Luo, S.1
Zheng, X.2
Cheng, J.-P.3
-
101
-
-
0036979260
-
Prolinecatalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6
-
Kotrusz, P.; Kmentová, I.; Gotov, B.; Toma, Š.; Solčániová, E. Prolinecatalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6. Chem. Commun. 2002, 8, 2510-2511.
-
(2002)
Chem. Commun.
, vol.8
, pp. 2510-2511
-
-
Kotrusz, P.1
Kmentová, I.2
Gotov, B.3
Toma, Š.4
Solčániová, E.5
-
102
-
-
0037175484
-
L-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric aldol reactions
-
Loh, T.-P.; Feng, L.-C.; Yang, H.-Y.; Yang, J.-Y. L-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric aldol reactions. Tetrahedron Lett. 2002, 43, 8741-8743.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 8741-8743
-
-
Loh, T.-P.1
Feng, L.-C.2
Yang, H.-Y.3
Yang, J.-Y.4
-
103
-
-
0142091320
-
Organocatalysis in Ionic Liquids: Highly Efficient l-Proline-Catalyzed Direct Asymmetric Mannich Reactions Involving Ketone and Aldehyde Nucleophiles
-
Chowdari, N. S.; Ramachary, D. B.; Barbas III, C. F. Organocatalysis in Ionic Liquids: Highly Efficient l-Proline-Catalyzed Direct Asymmetric Mannich Reactions Involving Ketone and Aldehyde Nucleophiles. Synlett 2003, 1906-1909.
-
(2003)
Synlett
, pp. 1906-1909
-
-
Chowdari, N.S.1
Ramachary, D.B.2
Barbas III, C.F.3
-
104
-
-
1942467938
-
Direct catalytic asymmetric cross-aldol reactions in ionic liquid media
-
Córdova, A. Direct catalytic asymmetric cross-aldol reactions in ionic liquid media. Tetrahedron Lett. 2004, 45, 3949-3952.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 3949-3952
-
-
Córdova, A.1
-
105
-
-
37249061303
-
L-Proline- Catalyzed Asymmetric Direct Aldol Reaction of Heteroaromatic Aldehydes and Acetone Improvement of Catalytic Efficiency In Ionic Liquid Bmim [BF4]
-
Reddy, K. R.; Chakrapani, L.; Ramani, T.; Rajasekhar, C. V. L-Proline- Catalyzed Asymmetric Direct Aldol Reaction of Heteroaromatic Aldehydes and Acetone: Improvement of Catalytic Efficiency in Ionic Liquid bmim [BF4]. Synth. Commun. 2007, 37, 4301-4307.
-
(2007)
Synth. Commun.
, vol.37
, pp. 4301-4307
-
-
Reddy, K.R.1
Chakrapani, L.2
Ramani, T.3
Rajasekhar, C.V.4
-
106
-
-
0038329193
-
Synthesis of fluorinated materials catalyzed by proline or antibody 38C2 in ionic liquid
-
Kitazume, T.; Jiang, Z.; Kasai, K.; Mihara, Y.; Suzuki, M. Synthesis of fluorinated materials catalyzed by proline or antibody 38C2 in ionic liquid. J. Fluor. Chem. 2003, 121, 205-212.
-
(2003)
J. Fluor. Chem.
, vol.121
, pp. 205-212
-
-
Kitazume, T.1
Jiang, Z.2
Kasai, K.3
Mihara, Y.4
Suzuki, M.5
-
107
-
-
53849119486
-
Proline-Catalyzed Asymmetric Aldol Reaction in Guanidine- Derived Ionic Liquids
-
Shah, J.; Blumenthal, H.; Yacob, Z.; Liebscher, J. Proline-Catalyzed Asymmetric Aldol Reaction in Guanidine- Derived Ionic Liquids. Adv. Synth. Catal. 2008, 350, 1267-1270.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1267-1270
-
-
Shah, J.1
Blumenthal, H.2
Yacob, Z.3
Liebscher, J.4
-
108
-
-
20044390053
-
Recycling Chiral Organocatalyst (4S)-Phenoxy-(S)-proline for Direct Asymmetric Aldol Reaction in Ionic Liquid (bmim)PF6
-
Liu, Y.-H.; Zhang, Y.-W.; Ding, Y.-P.; Shen, Z.-X.; Luo, X.-Q. Recycling Chiral Organocatalyst (4S)-Phenoxy-(S)-proline for Direct Asymmetric Aldol Reaction in Ionic Liquid (bmim)PF6. Chin. J. Chem. 2005, 23, 634-636.
-
(2005)
Chin. J. Chem.
, vol.23
, pp. 634-636
-
-
Liu, Y.-H.1
Zhang, Y.-W.2
Ding, Y.-P.3
Shen, Z.-X.4
Luo, X.-Q.5
-
109
-
-
16444382686
-
Asymmetric direct aldol reaction catalyzed by an L-prolinamide derivative: Considerable improvement of the catalytic efficiency in the ionic liquid
-
Guo, H.-M.; Cun, L.-F.; Gong, L.-Z.; Mi, A.-Q.; Jiang, Y.-Z. Asymmetric direct aldol reaction catalyzed by an L-prolinamide derivative: considerable improvement of the catalytic efficiency in the ionic liquid. Chem. Commun. 2005, 1450-1452.
-
Chem. Commun.
-
-
Guo, H.-M.1
Cun, L.-F.2
Gong, L.-Z.3
Mi, A.-Q.4
Jiang, Y.-Z.5
-
110
-
-
34848917067
-
-
1(R),2(R)-Bis[(S)-prolinamido]cyclohexane/[bmim][BF4] ionic liquid as an efficient catalytic system for direct asymmetric aldol reactions
-
Kucherenko, A. S.; Siyutkin, D. E.; Muraviev, V. O.; Struchkova, M. I.; Zlotin, S. G. 1(R),2(R)-Bis[(S)-prolinamido]cyclohexane/[bmim][BF4] ionic liquid as an efficient catalytic system for direct asymmetric aldol reactions Mendeleev Commun. 2007, 17, 277-278.
-
(2007)
Mendeleev Commun.
, vol.17
, pp. 277-278
-
-
Kucherenko, A.S.1
Siyutkin, D.E.2
Muraviev, V.O.3
Struchkova, M.I.4
Zlotin, S.G.5
-
111
-
-
62249178507
-
Asymmetric aldol condensation in an ionic liquid-water system catalyzed by (S)-prolinamide derivatives
-
Kucherenko, A.; Syutkin, D.; Zlotin, S. Asymmetric aldol condensation in an ionic liquid-water system catalyzed by (S)-prolinamide derivatives. Russ. Chem. Bull. 2008, 57, 591-594.
-
(2008)
Russ. Chem. Bull.
, vol.57
, pp. 591-594
-
-
Kucherenko, A.1
Syutkin, D.2
Zlotin, S.3
-
112
-
-
33748570123
-
Asymmetric Direct Aldol Reaction Catalysed by LProlinethioamides
-
Gryko, D.; Lipinski, R. Asymmetric Direct Aldol Reaction Catalysed by LProlinethioamides. Eur. J. Org. Chem. 2006, 2006, 3864-3876.
-
(2006)
Eur. J. Org. Chem.
, vol.2006
, pp. 3864-3876
-
-
Gryko, D.1
Lipinski, R.2
-
113
-
-
34447253242
-
Functional ionic liquid from biorenewable materials: Synthesis and application as a catalyst in direct aldol reactions
-
Hu, S.; Jiang, T.; Zhang, Z.; Zhu, A.; Han, B.; Song, J.; Xie, Y.; Li, W. Functional ionic liquid from biorenewable materials: synthesis and application as a catalyst in direct aldol reactions. Tetrahedron Lett. 2007, 48, 5613-5617.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 5613-5617
-
-
Hu, S.1
Jiang, T.2
Zhang, Z.3
Zhu, A.4
Han, B.5
Song, J.6
Xie, Y.7
Li, W.8
-
114
-
-
44249092052
-
A recyclable non-immobilized siloxy serine organocatalyst for the asymmetric direct aldol reaction
-
Teo, Y.-C.; Chua, G.-L. A recyclable non-immobilized siloxy serine organocatalyst for the asymmetric direct aldol reaction. Tetrahedron Lett. 2008, 49, 4235-4238.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4235-4238
-
-
Teo, Y.-C.1
Chua, G.-L.2
-
115
-
-
49149122925
-
-
Lombardo, M.; Easwara, S.; Filippo Pasia, C. T.; Dhavale, D. D. Protonated arginine and lysine as catalysts for the direct asymmetric aldol reaction in ionic liquids Tetrahedron 2008, 64, 9203-9207.
-
(2008)
Protonated Arginine and Lysine as Catalysts for the Direct Asymmetric Aldol Reaction in Ionic Liquids Tetrahedron
, vol.64
, pp. 9203-9207
-
-
Lombardo, M.1
Easwara, S.2
Filippo Pasia, C.T.3
Dhavale, D.D.4
-
116
-
-
31544443862
-
Supported Ionic Liquids. New Recyclable Materials for the L-Proline-Catalyzed Aldol Reaction
-
Gruttadauria, M.; Riela, S.; Aprile, C.; Lo Meo, P.; D'Anna, F.; Noto, R. Supported Ionic Liquids. New Recyclable Materials for the L-Proline-Catalyzed Aldol Reaction. Adv. Synth. Catal. 2006, 348, 82-92.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 82-92
-
-
Gruttadauria, M.1
Riela, S.2
Aprile, C.3
Lo Meo, P.4
D'Anna, F.5
Noto, R.6
-
117
-
-
34548394453
-
An Improved Protocol for the Direct Asymmetric Aldol Reaction in Ionic Liquids, Catalysed by Onium Ion-Tagged Prolines
-
Lombardo, M.; Pasi, F.; Easwar, S.; Trombini, C. An Improved Protocol for the Direct Asymmetric Aldol Reaction in Ionic Liquids, Catalysed by Onium Ion-Tagged Prolines. Adv. Synth. Catal. 2007, 349, 2061-2065.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2061-2065
-
-
Lombardo, M.1
Pasi, F.2
Easwar, S.3
Trombini, C.4
-
118
-
-
33947261745
-
Recyclable Asymmetric Cyclization in Ionic Liquid Catalyzed by an Amino Acid, Leading to a Wieland-Miescher Ketone Analogue
-
Nozawa, M.; Akita, T.; Hoshi, T.; Suzuki, T.; Hagiwara, H. Recyclable Asymmetric Cyclization in Ionic Liquid Catalyzed by an Amino Acid, Leading to a Wieland-Miescher Ketone Analogue. Synlett 2007, 2007, 661-663.
-
(2007)
Synlett
, vol.2007
, pp. 661-663
-
-
Nozawa, M.1
Akita, T.2
Hoshi, T.3
Suzuki, T.4
Hagiwara, H.5
-
119
-
-
48749103408
-
Glycine-promoted rapid synthesis of novel xanthene derivatives in ionic liquid
-
Kidwai, M.; Singhal, K.; Kukreja, S. Glycine-promoted rapid synthesis of novel xanthene derivatives in ionic liquid. Can. J. Chem. 2008, 86, 799-802.
-
(2008)
Can. J. Chem.
, vol.86
, pp. 799-802
-
-
Kidwai, M.1
Singhal, K.2
Kukreja, S.3
-
120
-
-
77953841300
-
A Green and Efficient Asymmetric Aldol Reaction Catalyzed by a Chiral Anion Modified Ionic Liquid
-
Qian, Y.; Zheng X.; Wang, Y. A Green and Efficient Asymmetric Aldol Reaction Catalyzed by a Chiral Anion Modified Ionic Liquid. Eur. J. Org. Chem. 2010, 3662-3677.
-
(2010)
Eur. J. Org. Chem.
, pp. 3662-3677
-
-
Qian, Y.1
Zheng, X.2
Wang, Y.3
-
121
-
-
77949391402
-
L-Arginine as a cost-effective and recyclable catalyst for the synthesis of α,β-unsaturated nitriles and ketones in an ionic liquid
-
Hu, Y.; Guan, Z.; He, Y.-H.; Louwagie, N.; Yao, M. J. L-Arginine as a cost-effective and recyclable catalyst for the synthesis of α,β-unsaturated nitriles and ketones in an ionic liquid. J. Chem. Res. 2010, 22-24.
-
(2010)
J. Chem. Res.
, pp. 22-24
-
-
Hu, Y.1
Guan, Z.2
He, Y.-H.3
Louwagie, N.4
Yao, M.J.5
-
122
-
-
0345529038
-
The Direct Organocatalytic Asymmetric Mannich Reaction: Unmodified Aldehydes as Nucleophiles
-
Notz, W.; Tanaka, F.; Watanabe, S.-i.; Chowdari, N. S.; Turner, J. M.; Thayumanavan, R.; Barbas, C. F. The Direct Organocatalytic Asymmetric Mannich Reaction: Unmodified Aldehydes as Nucleophiles. J. Org. Chem. 2003, 68, 9624-9634.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9624-9634
-
-
Notz, W.1
Tanaka, F.2
Watanabe, S.-I.3
Chowdari, N.S.4
Turner, J.M.5
Thayumanavan, R.6
Barbas, C.F.7
-
123
-
-
5144229459
-
The Scope of the Direct Proline- Catalyzed Asymmetric Addition of Ketones to Imines
-
Notz, W.; Watanabe, S.-i.; Chowdari, Naidu S.; Zhong, G.; Betancort, Juan M.; Tanaka, F.; III, Carlos F. B. The Scope of the Direct Proline- Catalyzed Asymmetric Addition of Ketones to Imines. Adv. Synth. Catal. 2004, 346, 1131-1140.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 1131-1140
-
-
Notz, W.1
Watanabe, S.-I.2
Chowdari, N.S.3
Zhong, G.4
Betancort, J.M.5
Tanaka, F.6
Iii Carlos, F.B.7
-
124
-
-
74549180991
-
2-Pyrrolidinecarboxylic Acid Ionic Liquid as a Highly Efficient Organocatalyst for the Asymmetric One-Pot Mannich Reaction
-
Zheng, X.; Qian, Y.-B.; Wang, Y. 2-Pyrrolidinecarboxylic Acid Ionic Liquid as a Highly Efficient Organocatalyst for the Asymmetric One-Pot Mannich Reaction. Eur. J. Org. Chem. 2010, 2010, 515-522.
-
(2010)
Eur. J. Org. Chem.
, vol.2010
, pp. 515-522
-
-
Zheng, X.1
Qian, Y.-B.2
Wang, Y.3
-
125
-
-
38349089956
-
Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselective anti-Mannich-Type Reactions: Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol
-
Zhang, H.; Mitsumori, S.; Utsumi, N.; Imai, M.; Garcia-Delgado, N.; Mifsud, M.; Albertshofer, K.; Cheong, P. H. Y.; Houk, K. N.; Tanaka, F.; Barbas, C. F. Catalysis of 3-Pyrrolidinecarboxylic Acid and Related Pyrrolidine Derivatives in Enantioselective anti-Mannich-Type Reactions: Importance of the 3-Acid Group on Pyrrolidine for Stereocontrol. J. Am. Chem. Soc. 2008, 130, 875-886.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 875-886
-
-
Zhang, H.1
Mitsumori, S.2
Utsumi, N.3
Imai, M.4
Garcia-Delgado, N.5
Mifsud, M.6
Albertshofer, K.7
Cheong, P.H.Y.8
Houk, K.N.9
Tanaka, F.10
Barbas, C.F.11
-
126
-
-
4043170073
-
Asymmetric Synthesis of Quaternary a- and ß-Amino Acids and ß -Lactams via Proline-Catalyzed Mannich Reactions with Branched Aldehyde Donors
-
Chowdari, N. S.; Suri, J. T.; Barbas, C. F. Asymmetric Synthesis of Quaternary a- and ß-Amino Acids and ß -Lactams via Proline-Catalyzed Mannich Reactions with Branched Aldehyde Donors. Org. Lett. 2004, 6, 2507-2510.
-
(2004)
Org. Lett.
, vol.6
, pp. 2507-2510
-
-
Chowdari, N.S.1
Suri, J.T.2
Barbas, C.F.3
-
127
-
-
76049098375
-
Asymmetric Mannich reaction catalyzed by N-arylsulfonyl-l-proline amides
-
Veverková, E.; Štrasserová, J.; Šebesta, R.; Toma, Š. Asymmetric Mannich reaction catalyzed by N-arylsulfonyl-l-proline amides. Tetrahedron: Asymmetry 2010, 21, 58-61.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 58-61
-
-
Veverková, E.1
Štrasserová, J.2
Šebesta, R.3
Toma, Š.4
-
128
-
-
77953311994
-
Highly efficient chemoselective construction of 2,2-dimethyl-6- substituted 4-piperidones via multi-component tandem Mannich reaction in ionic liquids
-
Feng, L.-C.; Sun, Y.-W.; Tang, W.-J.; Xu, L.-J.; Lam, K.-L.; Zho, Z.; Chan, A. S. C. Highly efficient chemoselective construction of 2,2-dimethyl-6- substituted 4-piperidones via multi-component tandem Mannich reaction in ionic liquids. Green Chem., 2010, 12, 949-952.
-
(2010)
Green Chem.
, vol.12
, pp. 949-952
-
-
Feng, L.-C.1
Sun, Y.-W.2
Tang, W.-J.3
Xu, L.-J.4
Lam, K.-L.5
Zho, Z.6
Chan, A.S.C.7
-
129
-
-
27844576639
-
Enantioselective organocatalysis in ionic liquids: Addition of aliphatic aldehydes and ketones to diethyl azodicarboxylate
-
Kotrusz, P.; Alemayehu, S.; Toma, Š.; Schmalz, H. G.; Adler, A. Enantioselective organocatalysis in ionic liquids: Addition of aliphatic aldehydes and ketones to diethyl azodicarboxylate. Eur. J. Org. Chem. 2005, 4904-4911.
-
(2005)
Eur. J. Org. Chem.
, pp. 4904-4911
-
-
Kotrusz, P.1
Alemayehu, S.2
Toma, Š.3
Schmalz, H.G.4
Adler, A.5
-
130
-
-
33750014954
-
Highly Enantioselective alpha- Aminoxylation of Aldehydes and Ketones in Ionic Liquids
-
Huang, K.; Huang, Z. Z.; Li, X. L. Highly Enantioselective alpha- Aminoxylation of Aldehydes and Ketones in Ionic Liquids. J. Org. Chem. 2006, 71, 8320-8323.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8320-8323
-
-
Huang, K.1
Huang, Z.Z.2
Li, X.L.3
-
131
-
-
33746690372
-
L-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric -aminoxylation of aldehydes and ketones
-
Guo, H.-M.; Niu, H.-Y.; Xue, M.-X.; Guo, Q.-X.; Cun, L.-F.; Mi, A.-Q.; Jiang, Y.-Z.; Wang, J.-J. L-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric -aminoxylation of aldehydes and ketones. Green Chem. 2006, 8, 682-684.
-
(2006)
Green Chem.
, vol.8
, pp. 682-684
-
-
Guo, H.-M.1
Niu, H.-Y.2
Xue, M.-X.3
Guo, Q.-X.4
Cun, L.-F.5
Mi, A.-Q.6
Jiang, Y.-Z.7
Wang, J.-J.8
-
132
-
-
4544281440
-
Michael additions of aldehydes and ketones to beta-nitrostyrenes in an ionic liquid
-
Kotrusz, P.; Toma, Š.; Schmalz, H. G.; Adler, A. Michael additions of aldehydes and ketones to beta-nitrostyrenes in an ionic liquid. Eur. J. Org. Chem. 2004, 1577-1583.
-
(2004)
Eur. J. Org. Chem.
, pp. 1577-1583
-
-
Kotrusz, P.1
Toma, Š.2
Schmalz, H.G.3
Adler, A.4
-
133
-
-
34548388393
-
Pyrrolidine-pyridinium based organocatalysts for highly enantioselective Michael addition of cyclohexanone to nitroalkenes
-
Xu, D.-Q.; Wang, B.-T.; Luo, S.-P.; Yue, H.-D.; Wang, L.-P.; Xu, Z.-Y. Pyrrolidine-pyridinium based organocatalysts for highly enantioselective Michael addition of cyclohexanone to nitroalkenes. Tetrahedron: Asymmetry 2007, 18, 1788-1794.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 1788-1794
-
-
Xu, D.-Q.1
Wang, B.-T.2
Luo, S.-P.3
Yue, H.-D.4
Wang, L.-P.5
Xu, Z.-Y.6
-
134
-
-
20344372440
-
An ionic liquid influenced L-proline catalysed asymmetric Michael addition of ketones to nitrostyrene
-
Rasalkar, M. S.; Potdar, M. K.; Mohile, S. S.; Salunkhe, M. M. An ionic liquid influenced L-proline catalysed asymmetric Michael addition of ketones to nitrostyrene. J. Mol. Catal. A: Chem. 2005, 235, 267-270.
-
(2005)
J. Mol. Catal. A: Chem.
, vol.235
, pp. 267-270
-
-
Rasalkar, M.S.1
Potdar, M.K.2
Mohile, S.S.3
Salunkhe, M.M.4
-
135
-
-
61949140878
-
Catalytic Properties of L-Proline for Asymmetric Michael Reaction in Ionic Liquid
-
Luo, S.-P.; Wang, L.-P.; Yue, H.-D.; Le, Z.-G.; Yang, W.-L.; Xu, D.-Q.; Xu, Z.-Y. Catalytic Properties of L-Proline for Asymmetric Michael Reaction in Ionic Liquid. Acta Chim. Sin. 2006, 14, 1483-1488.
-
(2006)
Acta Chim Sin.
, vol.14
, pp. 1483-1488
-
-
Luo, S.-P.1
Wang, L.-P.2
Yue, H.-D.3
Le, Z.-G.4
Yang, W.-L.5
Xu, D.-Q.6
Xu, Z.-Y.7
-
136
-
-
70349338482
-
Simple Chiral Pyrrolidine-Pyridine-Based Catalysts for Highly Enantioselective Michael Addition to Nitro Olefins
-
Xu, D.-Z.; Shi, S.; Wang, Y. Simple Chiral Pyrrolidine-Pyridine-Based Catalysts for Highly Enantioselective Michael Addition to Nitro Olefins. Eur. J. Org. Chem. 2009, 2009, 4848-4853.
-
(2009)
Eur. J. Org. Chem.
, vol.2009
, pp. 4848-4853
-
-
Xu, D.-Z.1
Shi, S.2
Wang, Y.3
-
137
-
-
33750091660
-
Ion-Supported Chiral Pyrrolidines as Enantioselective Catalysts for Direct Michael Addition of Nitroalkenes in [BMIm]PF6
-
Xu, D.; Luo, S.; Yue, H.; Wang, L.; Liu, Y.; Xu, Z. Ion-Supported Chiral Pyrrolidines as Enantioselective Catalysts for Direct Michael Addition of Nitroalkenes in [BMIm]PF6. Synlett 2006, 2569-2572.
-
(2006)
Synlett
, pp. 2569-2572
-
-
Xu, D.1
Luo, S.2
Yue, H.3
Wang, L.4
Liu, Y.5
Xu, Z.6
-
138
-
-
5444250671
-
Trends in Asymmetric Michael Reactions Catalysed by Tripeptides in Combination with an Achiral Additive in Different Solvents
-
Tsogoeva, Svetlana B.; Jagtap, Sunil B.; Ardemasova, Zoya A.; Kalikhevich, Victor N. Trends in Asymmetric Michael Reactions Catalysed by Tripeptides in Combination with an Achiral Additive in Different Solvents. Eur. J. Org. Chem. 2004, 4014-4019.
-
(2004)
Eur. J. Org. Chem.
, pp. 4014-4019
-
-
Tsogoeva, S.B.1
Jagtap, S.B.2
Ardemasova, Z.A.3
Kalikhevich, V.N.4
-
139
-
-
1842638567
-
Catalytic asymmetric 1,4- conjugate addition of unmodified aldehyde in ionic liquid J
-
Hagiwara, H.; Okabe, T.; Hoshi, T.; Suzuki, T. Catalytic asymmetric 1,4- conjugate addition of unmodified aldehyde in ionic liquid J. Mol. Catal. A: Chem. 2004, 214, 167-174.
-
(2004)
Mol. Catal. A: Chem.
, vol.214
, pp. 167-174
-
-
Hagiwara, H.1
Okabe, T.2
Hoshi, T.3
Suzuki, T.4
-
140
-
-
34250618376
-
Asymmetric Conjugate Addition of Ketones to beta-Nitrostyrenes by Means of 1,2-Amino-Alcohol-Derived Prolinamides as Bifunctional Catalysts
-
Almasi, D.; Alonso, D. A.; Gómez-Bengoa, E.; Nagel, Y.; Nájera, C. Asymmetric Conjugate Addition of Ketones to beta-Nitrostyrenes by Means of 1,2-Amino-Alcohol-Derived Prolinamides as Bifunctional Catalysts. Eur. J. Org. Chem. 2007, 2007, 2328-2343.
-
(2007)
Eur. J. Org. Chem.
, vol.2007
, pp. 2328-2343
-
-
Almasi, D.1
Alonso, D.A.2
Gómez-Bengoa, E.3
Nagel, Y.4
Nájera, C.5
-
141
-
-
48949114906
-
A mild and efficient procedure for asymmetric Michael additions of cyclohexanone to chalcones by an amino acid ionic liquid
-
Qian, Y.; Xiao, S.; Liu, L.; Wang, Y. A mild and efficient procedure for asymmetric Michael additions of cyclohexanone to chalcones by an amino acid ionic liquid. Tetrahedron: Asymmetry 2008, 18, 1515-1518.
-
(2008)
Tetrahedron: Asymmetry
, vol.18
, pp. 1515-1518
-
-
Qian, Y.1
Xiao, S.2
Liu, L.3
Wang, Y.4
-
142
-
-
53849131000
-
Enamine Catalysis in the Synthesis of Chiral Structural Analogues of gem-Bisphosphonates Known To Be Biologically Active
-
Barros, M. T.; Phillips, A. M. F. Enamine Catalysis in the Synthesis of Chiral Structural Analogues of gem-Bisphosphonates Known To Be Biologically Active. Eur. J. Org. Chem. 2008, 2008, 2525-2529.
-
(2008)
Eur. J. Org. Chem.
, vol.2008
, pp. 2525-2529
-
-
Barros, M.T.1
Phillips, A.M.F.2
-
143
-
-
33645281478
-
Michael addition of thiols to betaenones in ionic liquids with and without organocatalysts
-
Meciarová, M.; Toma, Š.; Kotrusz, P. Michael addition of thiols to betaenones in ionic liquids with and without organocatalysts. Org. Biomol. Chem. 2006, 4, 1420-1424.
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 1420-1424
-
-
Meciarová, M.1
Toma, Š.2
Kotrusz, P.3
-
144
-
-
33845652139
-
Michael addition of thiols to beta-enones: Is any catalyst necessary?
-
Meciarová, M.; Toma, Š. Michael addition of thiols to beta-enones: Is any catalyst necessary? Lett. Org. Chem. 2006, 3, 794-797.
-
(2006)
Lett. Org. Chem.
, vol.3
, pp. 794-797
-
-
Meciarová, M.1
Toma, Š.2
-
145
-
-
35649017665
-
Stereoselective Michael addition of carbonyl compounds to (E)-beta-nitrostyrene catalysed by Ntoluensulfonyl- l-proline amide in ionic liquids
-
Meciarová, M.; Hubinská, K.; Toma, Š.; Koch, B.; Berkessel, A. Stereoselective Michael addition of carbonyl compounds to (E)-beta-nitrostyrene catalysed by Ntoluensulfonyl- l-proline amide in ionic liquids. Monatsh. Chem. 2007, 138, 1181-1186.
-
(2007)
Monatsh. Chem.
, vol.138
, pp. 1181-1186
-
-
Meciarová, M.1
Hubinská, K.2
Toma, Š.3
Koch, B.4
Berkessel, A.5
-
146
-
-
53849084847
-
Kinetic Study of Michael Addition Catalyzed by N-Methylimidazole in Ionic Liquids: Residual N-Methylimidazole in Ionic Liquids as a Strong Base
-
Meciarová, M.; Cigán, M.; Toma, Š.; Gáplovský A. Kinetic Study of Michael Addition Catalyzed by N-Methylimidazole in Ionic Liquids: Residual N-Methylimidazole in Ionic Liquids as a Strong Base. Eur. J. Org. Chem. 2008, 2008, 4408-4411.
-
(2008)
Eur. J. Org. Chem.
, vol.2008
, pp. 4408-4411
-
-
Meciarová, M.1
Cigán, M.2
Toma, Š.3
Gáplovský, A.4
-
147
-
-
36849063211
-
On the characterization of some [bmim][X]/co-solvent binary mixtures: A multidisciplinary approach by using kinetic, spectrophotometric and conductometric investigations
-
D'Anna, F.; Frenna, V.; La Marca, S.; Noto, R.; Pace, V.; Spinelli, D. On the characterization of some [bmim][X]/co-solvent binary mixtures: a multidisciplinary approach by using kinetic, spectrophotometric and conductometric investigations. Tetrahedron 2008, 64, 672-680.
-
(2008)
Tetrahedron
, vol.64
, pp. 672-680
-
-
D'Anna, F.1
Frenna, V.2
la Marca, S.3
Noto, R.4
Pace, V.5
Spinelli, D.6
-
148
-
-
33846573334
-
Michael additions of methylene active compounds to chalcone in ionic liquids without any catalyst: The peculiar properties of ionic liquids
-
Meciarová, M.; Toma, Š. Michael additions of methylene active compounds to chalcone in ionic liquids without any catalyst: The peculiar properties of ionic liquids. Chem. Eur. J. 2007, 13, 1268-1272.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 1268-1272
-
-
Meciarová, M.1
Toma, Š.2
-
149
-
-
71849098979
-
Asymmetric organocatalyzed Michael addition of aldehydes to [beta]-nitrostyrene in ionic liquids
-
Meciarová, M.; Toma, Š.; Šebesta, R. Asymmetric organocatalyzed Michael addition of aldehydes to [beta]-nitrostyrene in ionic liquids. Tetrahedron: Asymmetry 2009, 20, 2403-2406.
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 2403-2406
-
-
Meciarová, M.1
Toma, Š.2
Šebesta, R.3
-
150
-
-
0000220483
-
Diamine-Catalyzed Asymmetric Michael Additions of Aldehydes and Ketones to Nitrostyrene
-
Alexakis, A.; Andrey, O. Diamine-Catalyzed Asymmetric Michael Additions of Aldehydes and Ketones to Nitrostyrene. Org. Lett. 2002, 4, 3611-3614;
-
(2002)
Org. Lett.
, vol.4
, pp. 3611-3614
-
-
Alexakis, A.1
Andrey, O.2
-
151
-
-
65949105703
-
Enantioselective Organocatalytic Michael Addition of Aldehydes to beta-Nitrostyrenes
-
Laars, M.; Ausmees, K.; Uudsemaa, M.; Tamm, T.; Kanger, T.; Lopp, M. Enantioselective Organocatalytic Michael Addition of Aldehydes to beta-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
-
152
-
-
33748791724
-
Highly Efficient Asymmetric Michael Addition of Aldehydes to Nitroalkenes Catalyzed by a Simple trans-4-Hydroxyprolylamide
-
Palomo, C.; Vera, S.; Mielgo, A.; Gómez-Bengoa, E. Highly Efficient Asymmetric Michael Addition of Aldehydes to Nitroalkenes Catalyzed by a Simple trans-4-Hydroxyprolylamide. Angew. Chem. Int. Ed. 2006, 45, 5984-5987.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5984-5987
-
-
Palomo, C.1
Vera, S.2
Mielgo, A.3
Gómez-Bengoa, E.4
-
153
-
-
5144224358
-
The Use of NAlkyl-2,2prime-bipyrrolidine Derivatives as Organocatalysts for the Asymmetric Michael Addition of Ketones and Aldehydes to Nitroolefins
-
Andrey, O.; Alexakis, A.; Tomassini, A.; Bernardinelli, G. The Use of NAlkyl-2,2prime-bipyrrolidine Derivatives as Organocatalysts for the Asymmetric Michael Addition of Ketones and Aldehydes to Nitroolefins. Adv. Synth. Catal. 2004, 346, 1147-1168.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 1147-1168
-
-
Andrey, O.1
Alexakis, A.2
Tomassini, A.3
Bernardinelli, G.4
-
154
-
-
22144459070
-
Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes
-
Hayashi, Y.; Gotoh, H.; Hayashi, T.; Shoji, M. Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes. Angew. Chem. Int. Ed. 2005, 44, 4212-4215.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 4212-4215
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
155
-
-
33747002158
-
Effective and recyclable dendritic catalysts for the direct asymmetric Michael addition of aldehydes to nitrostyrenes
-
Li, Y.; Liu, X.-Y.; Zhao, G. Effective and recyclable dendritic catalysts for the direct asymmetric Michael addition of aldehydes to nitrostyrenes. Tetrahedron: Asymmetry 2006, 17, 2034-2039.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2034-2039
-
-
Li, Y.1
Liu, X.-Y.2
Zhao, G.3
-
156
-
-
77957191209
-
Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of ß-alkoxyketones by oxa-Michael addition reactions
-
Guo, H.; Li, X.; Wang, J.-L.; Jin, X.-H.; Lin, X.-F. Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of ß-alkoxyketones by oxa-Michael addition reactions. Tetrahedron 2010, 66, 8300-8303;
-
(2010)
Tetrahedron
, vol.66
, pp. 8300-8303
-
-
Guo, H.1
Li, X.2
Wang, J.-L.3
Jin, X.-H.4
Lin, X.-F.5
-
157
-
-
78649330635
-
Chiral quaternary alkylammonium ionic liquid [Pro-dabco][BF4]: As a recyclable and highly efficient organocatalyst for asymmetric Michael addition reaction
-
Xu, D.-Z.; Liu, Y.; Shi, S.; Wang, Y. Chiral quaternary alkylammonium ionic liquid [Pro-dabco][BF4]: as a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions. Tetrahedron: Asymmetry 2010, 21, 2530-2534.
-
(2010)
Tetrahedron: Asymmetr
, vol.2
, pp. 2530-2533
-
-
Xu, D.Z.1
Liu, Y.2
Shi, S.3
Wang, Y.4
-
158
-
-
1642527461
-
Recycling Chiral Imidazolidin-4-one Catalyst for Asymmetric Diels-Alder Reactions: Screening of Various Ionic Liquids
-
Park, Jin K.; Sreekanth, P.; Kim, B. M. Recycling Chiral Imidazolidin-4-one Catalyst for Asymmetric Diels-Alder Reactions: Screening of Various Ionic Liquids. Adv. Synth. Catal. 2004, 346, 49-52.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 49-52
-
-
Park, J.K.1
Sreekanth, P.2
Kim, B.M.3
-
159
-
-
0141745638
-
Organocatalytic Asymmetric Domino Knoevenagel/Diels-Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane-1,5,9-triones
-
Ramachary, D. B.; Chowdari, N. S.; III, C. F. B. Organocatalytic Asymmetric Domino Knoevenagel/Diels-Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane-1,5,9-triones. Angew. Chem. Int. Ed. 2003, 42, 4233-4237.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 4233-4237
-
-
Ramachary, D.B.1
Chowdari, N.S.2
Iii, C.F.B.3
-
160
-
-
0142059749
-
The First Organocatalytic Hetero-Domino Knoevenagel-Diels-Alder-Epimerization Reactions: Diastereoselective Synthesis of Highly Substituted Spiro[cyclohexane-1,2??-indan]-1??,3??,4-triones
-
Ramachary, D. B.; Chowdari, N. S.; Barbas III, C. F. The First Organocatalytic Hetero-Domino Knoevenagel-Diels-Alder-Epimerization Reactions: Diastereoselective Synthesis of Highly Substituted Spiro[cyclohexane-1,2??-indan]-1??,3??,4-triones. Synlett 2003, 2003, 1910-1914.
-
(2003)
Synlett
, vol.2003
, pp. 1910-1914
-
-
Ramachary, D.B.1
Chowdari, N.S.2
Barbas III, C.F.3
-
161
-
-
8344250171
-
Towards Organo-Click Chemistry: Development of Organocatalytic Multicomponent Reactions Through Combinations of Aldol, Wittig, Knoevenagel, Michael, Diels-Alder and Huisgen Cycloaddition Reactions
-
Ramachary, D. B.; III, C. F. B. Towards Organo-Click Chemistry: Development of Organocatalytic Multicomponent Reactions Through Combinations of Aldol, Wittig, Knoevenagel, Michael, Diels-Alder and Huisgen Cycloaddition Reactions. Chem. Eur. J. 2004, 10, 5323-5331.
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 5323-5331
-
-
Ramachary, D.B.1
Iii, C.F.B.2
-
162
-
-
20444494428
-
Direct Asymmetric alpha-Fluorination of Aldehydes
-
Steiner, D. D.; Mase, N.; III, C. F. B. Direct Asymmetric alpha-Fluorination of Aldehydes. Angew. Chem. Int. Ed. 2005, 44, 3706-3710.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 3706-3710
-
-
Steiner, D.D.1
Mase, N.2
Iii, C.F.B.3
-
163
-
-
2342641980
-
Asymmetric aldol reactions in poly(ethylene glycol) catalyzed by l-proline
-
Chandrasekhar, S.; Narsihmulu, C.; Reddy, N. R.; Sultana, S. S. Asymmetric aldol reactions in poly(ethylene glycol) catalyzed by l-proline. Tetrahedron Lett. 2004, 45, 4581-4582.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4581-4582
-
-
Chandrasekhar, S.1
Narsihmulu, C.2
Reddy, N.R.3
Sultana, S.S.4
-
164
-
-
72649084416
-
A supramolecular hydrogel as a reusable heterogeneous catalyst for the direct aldol reaction
-
Rodríguez-Llansola, F.; Miravet, J. F.; Escuder, B. A supramolecular hydrogel as a reusable heterogeneous catalyst for the
-
(2009)
Chem. Commun.
, pp. 7303-7305
-
-
Rodríguez-Llansola, F.1
Miravet, J.F.2
Escuder, B.3
-
165
-
-
72649084416
-
supramolecular hydrogel as a reusable heterogeneous catalyst for the direct aldol reaction
-
Rodriquez-Llamsola, F.; Miravet, J. F.; Escuder, B. A supramolecular hydrogel as a reusable heterogeneous catalyst for the direct aldol reaction. Chem. Commun. 2009, 7303-7305.
-
(2009)
Chem. Commun.
, pp. 7303-7305
-
-
Rodriquez-Llamsola, F.1
Miravet, J.F.2
Escuder, B.A.3
-
166
-
-
77956712781
-
Cyclic carbonates as suitable solvents for proline-catalyzed aldol reaction
-
Clegg, W.; Harrington, R. W.; North, M.; Pizzato, F.; Villuendas, P. Cyclic carbonates as suitable solvents for proline-catalyzed aldol reaction. Tetrahedron: Asymmetry 2010, 21, 1262-1271;
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 1262-1271
-
-
Clegg, W.1
Harrington, R.W.2
North, M.3
Pizzato, F.4
Villuendas, P.5
-
167
-
-
77952329857
-
Chiral Solvent Effect in Asymmetric Organocatalysis
-
North, M.; Villuendas, P. A Chiral Solvent Effect in Asymmetric Organocatalysis. Org. Lett. 2010, 12, 2378-2381.
-
(2010)
Org. Lett.
, vol.12
, pp. 2378-2381
-
-
North, M.1
Villuendas, P.A.2
-
168
-
-
52049123632
-
Asymmetric Catalysis: Resin-Bound Hydroxyprolylthreonine Derivatives in Enamine-Mediated Reactions
-
Carpenter, Richard D.; Fettinger, James C.; Lam, Kit S.; Kurth, Mark J. Asymmetric Catalysis: Resin-Bound Hydroxyprolylthreonine Derivatives in Enamine-Mediated Reactions. Angew. Chem. Int. Ed. 2008, 47, 6407-6410.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6407-6410
-
-
Carpenter Richard, D.1
Fettinger, J.C.2
Lam Kit, S.3
Kurth, M.J.4
-
169
-
-
74049126344
-
Microwave-assisted organocatalytic multicomponent Knoevenagel/hetero Diels-Alder reaction for the synthesis of 2,3-dihydropyran[2,3-c]pyrazoles
-
Radi, M.; Bernardo, V.; Bechi, B.; Castagnolo, D.; Pagano, M.; Botta, M. Microwave-assisted organocatalytic multicomponent Knoevenagel/hetero Diels-Alder reaction for the synthesis of 2,3-dihydropyran[2,3-c]pyrazoles. Tetrahedron Lett. 2009, 50, 6572-6575.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 6572-6575
-
-
Radi, M.1
Bernardo, V.2
Bechi, B.3
Castagnolo, D.4
Pagano, M.5
Botta, M.6
-
170
-
-
67650484331
-
Asymmetric synthesis of 2-azabicyclo[3.3.1]nonanes by a microwave-assisted organocatalysed tandem desymmetrisation and intramolecular aldolisation
-
Diaba, F.; Bonjoch, J. Asymmetric synthesis of 2-azabicyclo[3.3.1]nonanes by a microwave-assisted organocatalysed tandem desymmetrisation and intramolecular aldolisation. Org. Biomol. Chem. 2009, 7, 2517-2519.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 2517-2519
-
-
Diaba, F.1
Bonjoch, J.2
-
171
-
-
33747205615
-
Organocatalyzed Asymmetric Reactions via Microwave Activation
-
Mosse, S.; Alexakis, A. Organocatalyzed Asymmetric Reactions via Microwave Activation. Org. Lett. 2006, 8, 3577-3580.
-
(2006)
Org. Lett.
, vol.8
, pp. 3577-3580
-
-
Mosse, S.1
Alexakis, A.2
-
172
-
-
33846986839
-
Microwave-Assisted Asymmetric Organocatalysis. A Probe for Nonthermal Microwave Effects and the Concept of Simultaneous Cooling
-
Hosseini, M.; Stiasni, N.; Barbieri, V.; Kappe, C. O. Microwave-Assisted Asymmetric Organocatalysis. A Probe for Nonthermal Microwave Effects and the Concept of Simultaneous Cooling. J. Org. Chem. 2007, 72, 1417-1424.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 1417-1424
-
-
Hosseini, M.1
Stiasni, N.2
Barbieri, V.3
Kappe, C.O.4
-
173
-
-
33645507049
-
Thermal Effects in the Organocatalytic Asymmetric Mannich Reaction
-
Rodriguez, B.; Bolm, C. Thermal Effects in the Organocatalytic Asymmetric Mannich Reaction. J. Org. Chem. 2006, 71, 2888-2891.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 2888-2891
-
-
Rodriguez, B.1
Bolm, C.2
-
174
-
-
53749097933
-
Thermal Effects in the Organocatalytic Asymmetric alpha-Amination of Disubstituted Aldehydes with Azodicarboxylates: A High-Temperature Organocatalysis
-
Baumann, T.; Bächle, M.; Hartmann, C.; Bräse, S. Thermal Effects in the Organocatalytic Asymmetric alpha-Amination of Disubstituted Aldehydes with Azodicarboxylates: A High-Temperature Organocatalysis. Eur. J. Org. Chem. 2008, 2207-2212.
-
(2008)
Eur. J. Org. Chem.
, pp. 2207-2212
-
-
Baumann, T.1
Bächle, M.2
Hartmann, C.3
Bräse, S.4
-
175
-
-
33748628266
-
Sulfamidation of 2-Arylaldehydes and Ketones with Chloramine-T
-
Baumann, T.; Bächle, M.; Bräse, S. Sulfamidation of 2-Arylaldehydes and Ketones with Chloramine-T. Org. Lett. 2006, 8, 3797-3800.
-
(2006)
Org. Lett.
, vol.8
, pp. 3797-3800
-
-
Baumann, T.1
Bächle, M.2
Bräse, S.3
-
176
-
-
37549035949
-
Microwave-Assisted Organocatalytic Anomerization of a-C-Glycosylmethyl Aldehydes and Ketones
-
Massi, A.; Nuzzi, A.; Dondoni, A. Microwave-Assisted Organocatalytic Anomerization of a-C-Glycosylmethyl Aldehydes and Ketones. J. Org. Chem. 2007, 72, 10279-10282.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 10279-10282
-
-
Massi, A.1
Nuzzi, A.2
Dondoni, A.3
-
177
-
-
38949140139
-
Asymmetric organocatalytic nitroaldol reaction of [alpha]-ketoesters: Stereoselective construction of chiral tertiary alcohols at subzero temperature
-
Takada, K.; Takemura, N.; Cho, K.; Sohtome, Y.; Nagasawa, K. Asymmetric organocatalytic nitroaldol reaction of [alpha]-ketoesters: stereoselective construction of chiral tertiary alcohols at subzero temperature. Tetrahedron Lett. 2008, 49, 1623-1626.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1623-1626
-
-
Takada, K.1
Takemura, N.2
Cho, K.3
Sohtome, Y.4
Nagasawa, K.5
-
178
-
-
66449097465
-
Efficient organocatalytic [alpha]-sulfenylation of substituted piperazine-2,5-diones
-
Dubey, R.; Polaske, N. W.; Nichol, G. S.; Olenyuk, B. Efficient organocatalytic [alpha]-sulfenylation of substituted piperazine-2,5-diones. Tetrahedron Lett. 2009, 50, 4310-4313.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 4310-4313
-
-
Dubey, R.1
Polaske, N.W.2
Nichol, G.S.3
Olenyuk, B.4
-
179
-
-
70349211623
-
Highly Enantioselective Organocatalytic Addition of Ethyl Trifluoropyruvate to Ketones with Subzero Temperature Microwave Activation
-
Landge, S.; Török, B. Highly Enantioselective Organocatalytic Addition of Ethyl Trifluoropyruvate to Ketones with Subzero Temperature Microwave Activation. Catal. Lett. 2009, 131, 432-439.
-
(2009)
Catal. Lett.
, vol.131
, pp. 432-439
-
-
Landge, S.1
Török, B.2
-
180
-
-
77954849793
-
A New Microwave-Assisted Organocatalytic Solvent-Free Synthesis of Optically Enriched Michael Adducts
-
Procopio, A.; De Nino, A.; Nardi, M.; Oliviero, M.; Paonessa, R.; Pasceri, R. A New Microwave-Assisted Organocatalytic Solvent-Free Synthesis of Optically Enriched Michael Adducts. Synlett 2010, 1849-1853;
-
(2010)
Synlett
, pp. 1849-1853
-
-
Procopio, A.1
de Nino, A.2
Nardi, M.3
Oliviero, M.4
Paonessa, R.5
Pasceri, R.6
-
181
-
-
76249097507
-
Microwave-Assisted Organocatalytic Quadrupole Domino Reactions of Acetaldehyde and Nitroalkenes
-
Enders, D.; Krüll, R.; Bettray, W. Microwave-Assisted Organocatalytic Quadrupole Domino Reactions of Acetaldehyde and Nitroalkenes. Synthesis 2010, 567-572.
-
(2010)
Synthesis
, pp. 567-572
-
-
Enders, D.1
Krüll, R.2
Bettray, W.3
-
182
-
-
0037175462
-
The Baylis-Hillman reaction under high pressure induced by water-freezing
-
Hayashi, Y.; Okado, K.; Ashimine, I.; Shoji, M. The Baylis-Hillman reaction under high pressure induced by water-freezing. Tetrahedron Lett. 2002, 43, 8683-8686.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 8683-8686
-
-
Hayashi, Y.1
Okado, K.2
Ashimine, I.3
Shoji, M.4
-
183
-
-
0043194285
-
Application of High Pressure Induced by Water-Freezing to the Direct Catalytic Asymmetric Three- Component List-Barbas-Mannich Reaction
-
Hayashi, Y.; Tsuboi, W.; Shoji, M.; Suzuki, N. Application of High Pressure Induced by Water-Freezing to the Direct Catalytic Asymmetric Three- Component List-Barbas-Mannich Reaction. J. Am. Chem. Soc. 2003, 125, 11208-11209.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11208-11209
-
-
Hayashi, Y.1
Tsuboi, W.2
Shoji, M.3
Suzuki, N.4
-
184
-
-
2342605494
-
Application of high pressure, induced by water freezing, to the direct asymmetric aldol reaction
-
Hayashi, Y.; Tsuboi, W.; Shoji, M.; Suzuki, N. Application of high pressure, induced by water freezing, to the direct asymmetric aldol reaction. Tetrahedron Lett. 2004, 45, 4353-4356.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4353-4356
-
-
Hayashi, Y.1
Tsuboi, W.2
Shoji, M.3
Suzuki, N.4
-
185
-
-
0042912970
-
High- Pressure-Promoted Asymmetric Aldol Reactions of Ketones with Aldehydes Catalyzed by l-Proline
-
Sekiguchi, Y.; Sasaoka, A.; Shimomoto, A.; Fujioka, S.; Kotsuki, H. High- Pressure-Promoted Asymmetric Aldol Reactions of Ketones with Aldehydes Catalyzed by l-Proline. Synlett 2003, 2003, 1655-1658.
-
(2003)
Synlett
, vol.2003
, pp. 1655-1658
-
-
Sekiguchi, Y.1
Sasaoka, A.2
Shimomoto, A.3
Fujioka, S.4
Kotsuki, H.5
-
186
-
-
28944440486
-
Synthesis of (-)- (5R,6S)-6-acetoxyhexadecanolide based on l-proline-catalyzed asymmetric aldol reactions
-
Ikishima, H.; Sekiguchi, Y.; Ichikawa, Y.; Kotsuki, H. Synthesis of (-)- (5R,6S)-6-acetoxyhexadecanolide based on l-proline-catalyzed asymmetric aldol reactions. Tetrahedron 2006, 62, 311-316.
-
(2006)
Tetrahedron
, vol.62
, pp. 311-316
-
-
Ikishima, H.1
Sekiguchi, Y.2
Ichikawa, Y.3
Kotsuki, H.4
-
187
-
-
69449105547
-
Efficient Organocatalytic Hetero-Diels-Alder Reactions of Activated Ketones under High Pressure for Direct Access to d-Lactones
-
Mori, K.; Maddaluno, J.; Nakano, K.; Ichikawa, Y.; Kotsuki, H. Efficient Organocatalytic Hetero-Diels-Alder Reactions of Activated Ketones under High Pressure for Direct Access to d-Lactones. Synlett 2009, 2009, 2346-2350.
-
(2009)
Synlett
, vol.2009
, pp. 2346-2350
-
-
Mori, K.1
Maddaluno, J.2
Nakano, K.3
Ichikawa, Y.4
Kotsuki, H.5
-
188
-
-
54949089047
-
Organocatalytic reactions: Effects of ball milling, microwave and ultrasound irradiation
-
Bruckmann, A.; Krebs, A.; Bolm, C. Organocatalytic reactions: effects of ball milling, microwave and ultrasound irradiation. Green Chem. 2008, 10, 1131-1141.
-
(2008)
Green Chem.
, vol.10
, pp. 1131-1141
-
-
Bruckmann, A.1
Krebs, A.2
Bolm, C.3
-
189
-
-
0037627742
-
The Use of DMAP as Catalyst in the Baylis-Hillman Reaction Between Methyl Acrylate and Aromatic Aldehydes
-
Octavio, R.; de Souza, M. A.; Vasconcellos, M. L. A. A. The Use of DMAP as Catalyst in the Baylis-Hillman Reaction Between Methyl Acrylate and Aromatic Aldehydes. Synth. Commun. 2003, 33, 1383 - 1389.
-
(2003)
Synth. Commun.
, vol.33
, pp. 1383-1389
-
-
Octavio, R.1
de Souza, M.A.2
Vasconcellos, M.L.A.A.3
-
190
-
-
0037467814
-
An easy and stereoselective synthesis of NBoc- dolaproine via the Baylis-Hillman reaction
-
Almeida, W. P.; Coelho, F. An easy and stereoselective synthesis of NBoc- dolaproine via the Baylis-Hillman reaction. Tetrahedron Lett. 2003, 44, 937-940;
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 937-940
-
-
Almeida, W.P.1
Coelho, F.2
-
191
-
-
33344473974
-
The Baylis-Hillman Reaction with Chiral ??-Amino Aldehydes under Racemization-Free Conditions
-
Coelho, F.; Diaz, G.; Abella, C. A. M.; Almeida, W. P. The Baylis-Hillman Reaction with Chiral ??-Amino Aldehydes under Racemization-Free Conditions. Synlett 2006, 2006, 0435-0439.
-
(2006)
Synlett
, vol.2006
, pp. 0435-0439
-
-
Coelho, F.1
Diaz, G.2
Abella, C.A.M.3
Almeida, W.P.4
-
192
-
-
33745712182
-
Proline catalyzed two-component, three-component and self-asymmetric Mannich reactions promoted by ultrasonic conditions
-
Kantam, M. L.; Rajasekhar, C. V.; Gopikrishna, G.; Rajender Reddy, K.; Choudary, B. M. Proline catalyzed two-component, three-component and self-asymmetric Mannich reactions promoted by ultrasonic conditions. Tetrahedron Lett. 2006, 47, 5965-5967.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 5965-5967
-
-
Kantam, M.L.1
Rajasekhar, C.V.2
Gopikrishna, G.3
Rajender, R.K.4
Choudary, B.M.5
-
193
-
-
33750460594
-
Solvent-Free Asymmetric Organocatalysis in a Ball Mill
-
Rodríguez, B.; Rantanen, T.; Bolm, C. Solvent-Free Asymmetric Organocatalysis in a Ball Mill. Angew. Chem. Int. Ed. 2006, 45, 6924-6926.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6924-6926
-
-
Rodríguez, B.1
Rantanen, T.2
Bolm, C.3
-
194
-
-
34250371777
-
Highly Efficient Asymmetric Organocatalytic Aldol Reaction in a Ball Mill
-
Rodríguez, B.; Bruckmann, A.; Bolm, C. A Highly Efficient Asymmetric Organocatalytic Aldol Reaction in a Ball Mill. Chem. Eur. J. 2007, 13, 4710-4722.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 4710-4722
-
-
Rodríguez, B.1
Bruckmann, A.2
Bolm, C.A.3
-
195
-
-
60849136349
-
Nonlinear effects in prolinecatalysed aldol reactions under solvent-free conditions based on the ternary phase behaviour of scalemic proline
-
Bruckmann, A.; Rodríguez, B.; Bolm, C. Nonlinear effects in prolinecatalysed aldol reactions under solvent-free conditions based on the ternary phase behaviour of scalemic proline. CrystEngComm 2009, 11, 404-407.
-
(2009)
CrystEngComm
, vol.11
, pp. 404-407
-
-
Bruckmann, A.1
Rodríguez, B.2
Bolm, C.3
-
196
-
-
35348873830
-
Solventfree asymmetric direct aldol reactions organocatalysed by recoverable S - binam-l-prolinamide
-
Guillena, G.; del Carmen Hita, M.; Nájera, C.; Viózquez, S. F. Solventfree asymmetric direct aldol reactions organocatalysed by recoverable S - binam-l-prolinamide. Tetrahedron: Asymmetry 2007, 18, 2300-2304;
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2300-2304
-
-
Guillena, G.1
del Carmen Hita, M.2
Nájera, C.3
Viózquez, S.F.4
-
197
-
-
48249091272
-
A Highly Efficient Solvent-Free Asymmetric Direct Aldol Reaction Organocatalyzed by Recoverable (S)-Binam-l-Prolinamides. ESI-MS Evidence of the Enamine-Iminium Formation
-
Guillena, G.; Hita, M. d. C.; Nájera, C.; Viózquez, S. F. A Highly Efficient Solvent-Free Asymmetric Direct Aldol Reaction Organocatalyzed by Recoverable (S)-Binam-l-Prolinamides. ESI-MS Evidence of the Enamine-Iminium Formation. J. Org. Chem. 2008, 73, 5933-5943.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 5933-5943
-
-
Guillena, G.1
Hita, M.D.C.2
Nájera, C.3
Viózquez, S.F.4
-
198
-
-
35348885188
-
Solvent-Free Asymmetric Anhydride Opening in a Ball Mill
-
Rantanen, T.; Schiffers, I.; Bolm, C. Solvent-Free Asymmetric Anhydride Opening in a Ball Mill. Org. Proc. Res. Dev. 2007, 11, 592-597.
-
(2007)
Org. Proc. Res. Dev.
, vol.11
, pp. 592-597
-
-
Rantanen, T.1
Schiffers, I.2
Bolm, C.3
-
199
-
-
34047094942
-
Rate enhancement of the Morita-Baylis-Hillman reaction through mechanochemistry
-
Mack, J.; Shumba, M. Rate enhancement of the Morita-Baylis-Hillman reaction through mechanochemistry. Green Chem. 2007, 9, 328-330.
-
(2007)
Green Chem.
, vol.9
, pp. 328-330
-
-
Mack, J.1
Shumba, M.2
-
200
-
-
33746903576
-
Solventless Protocol for Efficient Bis-N-Boc Protection of Adenosine, Cytidine, and Guanosine Derivatives
-
Sikchi, S. A.; Hultin, P. G. Solventless Protocol for Efficient Bis-N-Boc Protection of Adenosine, Cytidine, and Guanosine Derivatives. J. Org. Chem. 2006, 71, 5888-5891.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 5888-5891
-
-
Sikchi, S.A.1
Hultin, P.G.2
-
201
-
-
60949084915
-
An efficient ultrasound-promoted synthesis of the Baylis-Hillman adducts catalyzed by imidazole and l-proline
-
Mamaghani, M.; Dastmard, S. An efficient ultrasound-promoted synthesis of the Baylis-Hillman adducts catalyzed by imidazole and l-proline. Ultrason. Sonochem. 2009, 16, 445-447.
-
(2009)
Ultrason. Sonochem.
, vol.16
, pp. 445-447
-
-
Mamaghani, M.1
Dastmard, S.2
|