-
1
-
-
0141619399
-
Polymer-Supported organic catalysts
-
Benaglia M., Puglisi A., Cozzi F., Polymer-Supported organic catalysts, Chem. Rev., 103, 3401-3429, 2003.
-
(2003)
Chem. Rev
, vol.103
, pp. 3401-3429
-
-
Benaglia, M.1
Puglisi, A.2
Cozzi, F.3
-
2
-
-
0000677232
-
Organic reactions in aqueous media-with a focus on carbon-carbon bond formation
-
Li C. J., Organic reactions in aqueous media-with a focus on carbon-carbon bond formation, Chem. Rev., 93, 2023-2035, 1993.
-
(1993)
Chem. Rev
, vol.93
, pp. 2023-2035
-
-
Li, C.J.1
-
3
-
-
0027934153
-
Water promoted organic reactions
-
Lubineau A., Augé J., Queneau Y., Water promoted organic reactions, Synthesis, 741-760, 1994.
-
(1994)
Synthesis
, vol.741-760
-
-
Lubineau, A.1
Augé, J.2
Queneau, Y.3
-
4
-
-
0000159773
-
The Michael reaction
-
Bergmann E. D., Ginsburg D., Pappo R. The Michael reaction, Org. React., 10, 179-569, 1959.
-
(1959)
Org. React
, vol.10
, pp. 179-569
-
-
Bergmann, E.D.1
Ginsburg, D.2
Pappo, R.3
-
5
-
-
0037152336
-
7, A new catalyst for Michael addition
-
7, A new catalyst for Michael addition, Tetrahedron Lett., 43, 7729-7730, 2002.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 7729-7730
-
-
Zahouily, M.1
Abrouki, Y.2
Rayadh, A.3
-
6
-
-
0030750993
-
Zeolite mediated Michael addition of 1,3-dicarbonyl compounds and thiols
-
Sreekurnar R., Rugmimi P., Padmakumar R., Zeolite mediated Michael addition of 1,3-dicarbonyl compounds and thiols, Tetrahedron Lett., 38, 6557-6560, 1997.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 6557-6560
-
-
Sreekurnar, R.1
Rugmimi, P.2
Padmakumar, R.3
-
7
-
-
0025146306
-
Dual catalysis of the Michael reaction
-
Laszlo P., Montaufier P. M. T., Randriamahefa S. L., Dual catalysis of the Michael reaction. Tetrahedron Lett., 31, 4867-4870, 1990.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 4867-4870
-
-
Laszlo, P.1
Montaufier, P.M.T.2
Randriamahefa, S.L.3
-
8
-
-
0032482490
-
Supported phenolates as efficient catalysts of the Michael reaction
-
Macquarrie D. J., Supported phenolates as efficient catalysts of the Michael reaction, Tetrahedron Lett., 39, 4125-4128, 1998.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4125-4128
-
-
Macquarrie, D.J.1
-
9
-
-
1542709349
-
Supported binolate salts as base catalysts. Preparation and use in the Michael reaction
-
Macquarrie D. J., Supported binolate salts as base catalysts. Preparation and use in the Michael reaction, Chem. Commun., 6, 601-602, 1997.
-
(1997)
Chem. Commun
, vol.6
, pp. 601-602
-
-
Macquarrie, D.J.1
-
10
-
-
14844312173
-
Asymmetric synthesis of ß-amino acids and α-substituted â-amino acids
-
Cardillo G., Tomasini C., Asymmetric synthesis of ß-amino acids and α-substituted â-amino acids, Chem. Soc. Rev., 117-128, 1996.
-
(1996)
Chem. Soc. Rev
, vol.117-128
-
-
Cardillo, G.1
Tomasini, C.2
-
11
-
-
33846080721
-
-
In Fluharty A. L., The Chemistry of the Thiol Group, Patai S., Ed., Wiely, New York, Part 2, 589, 1974.
-
In Fluharty A. L., The Chemistry of the Thiol Group, Patai S., Ed., Wiely, New York, Part 2, 589, 1974.
-
-
-
-
12
-
-
0033804490
-
The asymmetric synthesis of ß-haloaryl-ß-amino acid derivatives
-
Bull S. D., Davies S. G., Delgado-Ballester S., Fenton G., Kelly P. M., Smith A. D., The asymmetric synthesis of ß-haloaryl-ß-amino acid derivatives, Synlett, 1257-1260, 2000.
-
(2000)
Synlett
, vol.1257-1260
-
-
Bull, S.D.1
Davies, S.G.2
Delgado-Ballester, S.3
Fenton, G.4
Kelly, P.M.5
Smith, A.D.6
-
13
-
-
33846093623
-
An asymmetric synthesis of N-protected ß-amino aldehydes and ß-amino ketones
-
Davies S. G., McCarthy T. D., An asymmetric synthesis of N-protected ß-amino aldehydes and ß-amino ketones, Synlett, 700-702, 1995.
-
(1995)
Synlett
, vol.700-702
-
-
Davies, S.G.1
McCarthy, T.D.2
-
14
-
-
0032577033
-
A catalytic Michael addition of thiols to α,ß-unsaturated carbonyl compounds: Asymmetric michael additions and asymmetric protonations
-
Emori E., Arai Sasai T. H., Shibasaki, M., A catalytic Michael addition of thiols to α,ß-unsaturated carbonyl compounds: Asymmetric michael additions and asymmetric protonations, J. Am. Chem. Soc., 120, 4043-4044, 1998.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 4043-4044
-
-
Emori, E.1
Arai Sasai, T.H.2
Shibasaki, M.3
-
15
-
-
0037010780
-
Natural phosphate and doped-catalyzed michael addition of mercaptans to α,â -unsaturated carbonyl compounds
-
Abrouki Y., Zahouily M., Rayadh A., Bahlaouan B., Sebti S., Natural phosphate and doped-catalyzed michael addition of mercaptans to α,â -unsaturated carbonyl compounds, Tetrahedron Lett., 43, 8951-8953, 2002.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8951-8953
-
-
Abrouki, Y.1
Zahouily, M.2
Rayadh, A.3
Bahlaouan, B.4
Sebti, S.5
-
16
-
-
0013813289
-
The synthesis of ß-amino mercaptans and ß-amino thiosulfates via ethylenimine intermediates
-
Rosental d., braundrup G., Davis K. H., Wall M. E., The synthesis of ß-amino mercaptans and ß-amino thiosulfates via ethylenimine intermediates, J. Org. Chem., 30, 3689-3696, 1965.
-
(1965)
J. Org. Chem
, vol.30
, pp. 3689-3696
-
-
Rosental, D.1
braundrup, G.2
Davis, K.H.3
Wall, M.E.4
-
17
-
-
0037205013
-
3-catalyzed 1,4- then 1,2-nucleophilic addition to enones
-
3-catalyzed 1,4- then 1,2-nucleophilic addition to enones, J. Org. Chem., 67, 3700-3704, 2002.
-
(2002)
J. Org. Chem
, vol.67
, pp. 3700-3704
-
-
Bandini, M.1
Cozzi, P.G.2
Giacomini, M.3
Melchiorre, P.4
Selva, S.5
Umani-Ronchi, A.6
-
18
-
-
0037459683
-
Bismuth nitrate-catalyzed versatile Michael reactions
-
Srivastava N., Banic K., Bismuth nitrate-catalyzed versatile Michael reactions, J. Org. Chem., 68, 2109-2114, 2003.
-
(2003)
J. Org. Chem
, vol.68
, pp. 2109-2114
-
-
Srivastava, N.1
Banic, K.2
-
19
-
-
13844269067
-
40 A useful recyclable heterogeneous catalyst for the facile and highly efficient Michael addition reaction of thiols to α,ß-unsaturated ktones
-
40 A useful recyclable heterogeneous catalyst for the facile and highly efficient Michael addition reaction of thiols to α,ß-unsaturated ktones, Synlett, 299, 2005.
-
(2005)
Synlett
, vol.299
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafari, A.A.3
-
20
-
-
0346749656
-
Efficient copper-catalyzed chemo selective conjugate addition of aliphatic amines to α,ß-unsaturated compounds in water
-
Xu L. W., Li J. W., Xia C. G., Zhou S. L., Hu X. X. Efficient copper-catalyzed chemo selective conjugate addition of aliphatic amines to α,ß-unsaturated compounds in water, Synlett, 2425-2427, 2003.
-
(2003)
Synlett
, vol.2425-2427
-
-
Xu, L.W.1
Li, J.W.2
Xia, C.G.3
Zhou, S.L.4
Hu, X.X.5
-
21
-
-
3142703700
-
Transition-metal-based lewis acid catalysis of aza-type Michael additions of amines to α,ß-unsaturated electrophiles in water
-
Xu L. W., Li L., Xia C. G., Transition-metal-based lewis acid catalysis of aza-type Michael additions of amines to α,ß-unsaturated electrophiles in water, Helv. Chim. Acta, 87, 1522-1526, 2004.
-
(2004)
Helv. Chim. Acta
, vol.87
, pp. 1522-1526
-
-
Xu, L.W.1
Li, L.2
Xia, C.G.3
-
22
-
-
18244393705
-
Micellar solution of sodium dodecyl sulfate SDS catalyzes facile Michael addition of amines and thiols to α, ß-unsaturated ketones in water under neutral conditions
-
Firouzabadi H., Iranpoor N., Jafari A. A. Micellar solution of sodium dodecyl sulfate SDS catalyzes facile Michael addition of amines and thiols to α, ß-unsaturated ketones in water under neutral conditions, Adv. Synth. Catal., 347, 655-661, 2005.
-
(2005)
Adv. Synth. Catal
, vol.347
, pp. 655-661
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafari, A.A.3
-
23
-
-
11844279065
-
-
2O/NaI system supported on alumina in solvent-free conditions, J. Org. Chem., 70, 169-174, 2005.
-
2O/NaI system supported on alumina in solvent-free conditions, J. Org. Chem., 70, 169-174, 2005.
-
-
-
-
24
-
-
1542269183
-
A green, ionic liquid and quaternary ammonium salt-catalyzed aza-Michael reaction of α,ß- ethylenic compounds with amines in water
-
Xu L. W., Li J. W., Zhou S. L., Xia C. G., A green, ionic liquid and quaternary ammonium salt-catalyzed aza-Michael reaction of α,ß- ethylenic compounds with amines in water, New. J. Chem., 28, 183-184, 2004.
-
(2004)
New. J. Chem
, vol.28
, pp. 183-184
-
-
Xu, L.W.1
Li, J.W.2
Zhou, S.L.3
Xia, C.G.4
-
25
-
-
0035796966
-
Mild chemo-enzymatic synthesis of polymer-supported cinchona alkaloids and their application in asymmetric Michael addition
-
Athawal V., Manjrekar N., Mild chemo-enzymatic synthesis of polymer-supported cinchona alkaloids and their application in asymmetric Michael addition, Tetrahedron Lett., 42, 4541-4543, 2001.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 4541-4543
-
-
Athawal, V.1
Manjrekar, N.2
-
26
-
-
0035935120
-
Clay catalyzed chemoselective Michael type addition of aliphatic amines to α,ß- ethylenic compounds
-
Shaikh N. S., Deshpande V. H., Bedekar A. V., Clay catalyzed chemoselective Michael type addition of aliphatic amines to α,ß- ethylenic compounds, Tetrahedron, 57, 9045-9048, 2001.
-
(2001)
Tetrahedron
, vol.57
, pp. 9045-9048
-
-
Shaikh, N.S.1
Deshpande, V.H.2
Bedekar, A.V.3
-
27
-
-
0002174832
-
Polystyrene-supported ammonium fluoride as a catalyst for several base-catalyzed reactions
-
Ohtani N., Inoue Y., Nomoto A., Ohta S., Polystyrene-supported ammonium fluoride as a catalyst for several base-catalyzed reactions, React. Polym., 24, 73-78, 1994.
-
(1994)
React. Polym
, vol.24
, pp. 73-78
-
-
Ohtani, N.1
Inoue, Y.2
Nomoto, A.3
Ohta, S.4
-
28
-
-
0033305826
-
Organic reaction in water. Part 2: Michael addition in water without phase transfer agents
-
Martins da Silva, F., Gomes A. K., Jones J., Organic reaction in water. Part 2: Michael addition in water without phase transfer agents, Can. J. Chem., 77, 624-627, 1999.
-
(1999)
Can. J. Chem
, vol.77
, pp. 624-627
-
-
Martins da Silva, F.1
Gomes, A.K.2
Jones, J.3
-
29
-
-
0036535478
-
Synthesis of halohydrins from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new solid-liquid phase transfer catalyst
-
Tamami B., Mahdavi H., Synthesis of halohydrins from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new solid-liquid phase transfer catalyst, React. Funct. Polym., 5, 7-13, 2002.
-
(2002)
React. Funct. Polym
, vol.5
, pp. 7-13
-
-
Tamami, B.1
Mahdavi, H.2
-
30
-
-
0035802996
-
Synthesis of azidohydrins from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new polymeric phase-transfer catalyst
-
Tamami B., Mahdavi H., Synthesis of azidohydrins from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new polymeric phase-transfer catalyst, Tetrahedron Lett., 42, 8721-8724, 2001.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 8721-8724
-
-
Tamami, B.1
Mahdavi, H.2
-
31
-
-
1642497625
-
Synthesis of thiiranes from oxiranes in water using polymeric cosolvents
-
Tamami B., Kolahdoozan M., Synthesis of thiiranes from oxiranes in water using polymeric cosolvents, Tetrahedron Lett., 42, 1535-1537, 2004.
-
(2004)
Tetrahedron Lett
, vol.42
, pp. 1535-1537
-
-
Tamami, B.1
Kolahdoozan, M.2
-
32
-
-
1542604374
-
Regioselective azidolysis of epoxides in water using poly(vinylamine) and poly(allylamine) as new polymeric cosolvents
-
Tamami B., Kolahdoozan M. Mahdavi H., Regioselective azidolysis of epoxides in water using poly(vinylamine) and poly(allylamine) as new polymeric cosolvents, Iran. Polym. J., 13, 21-28, 2004.
-
(2004)
Iran. Polym. J
, vol.13
, pp. 21-28
-
-
Tamami, B.1
Kolahdoozan, M.2
Mahdavi, H.3
-
33
-
-
26844528493
-
A polymeric heterogeneous catalyst based on polyacrylamide for Knoevenagel reaction in solvent free and aqueous medias
-
Tamami B., Fadavi A., A polymeric heterogeneous catalyst based on polyacrylamide for Knoevenagel reaction in solvent free and aqueous medias, Iran. Polym. J., 6, 747-751, 2005.
-
(2005)
Iran. Polym. J
, vol.6
, pp. 747-751
-
-
Tamami, B.1
Fadavi, A.2
-
34
-
-
24344453789
-
Synthesis of 2-nitroalcohols from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new polymeric phase transfer catalyst
-
Tamami B., Mahdavi H., Synthesis of 2-nitroalcohols from epoxides using quaternized amino functionalized cross-linked polyacrylamide as a new polymeric phase transfer catalyst, React. Funct. Polym., 64, 179-185, 2005.
-
(2005)
React. Funct. Polym
, vol.64
, pp. 179-185
-
-
Tamami, B.1
Mahdavi, H.2
-
35
-
-
0035966174
-
-
2O-NaI system supported in silica gel, J. Org. Chem., 66, 9052-9055, 2001.
-
2O-NaI system supported in silica gel, J. Org. Chem., 66, 9052-9055, 2001.
-
-
-
-
36
-
-
0028130028
-
Recent stereoselective synthetic approaches to ß-amino acids
-
Cole D. E., Recent stereoselective synthetic approaches to ß-amino acids, Tetrahedron, 50, 9517-9582, 1994.
-
(1994)
Tetrahedron
, vol.50
, pp. 9517-9582
-
-
Cole, D.E.1
-
37
-
-
0000962863
-
Oxidative functionalization of the ß-carbon in α,ß-unsaturated systems: Preparation of 3-phenylthio enones, acrylates, and other vinyl derivatives
-
Bakuzis P., Bakuzis M. L. F., Oxidative functionalization of the ß-carbon in α,ß-unsaturated systems: Preparation of 3-phenylthio enones, acrylates, and other vinyl derivatives, J. Org. Chem., 46, 235-239, 1981.
-
(1981)
J. Org. Chem
, vol.46
, pp. 235-239
-
-
Bakuzis, P.1
Bakuzis, M.L.F.2
-
38
-
-
0037474595
-
Catalysis by an ionic liquid: Efficient conjugate addition of thiols to electron deficient alkenes catalyzed by molten tetrabutylammonium bromide under solvent-free conditions
-
Ranu B. C., Dey S. S., Hajra A., Catalysis by an ionic liquid: Efficient conjugate addition of thiols to electron deficient alkenes catalyzed by molten tetrabutylammonium bromide under solvent-free conditions, Tetrahedron, 59, 2417-2421, 2003.
-
(2003)
Tetrahedron
, vol.59
, pp. 2417-2421
-
-
Ranu, B.C.1
Dey, S.S.2
Hajra, A.3
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