-
1
-
-
0000695099
-
Chemical aspects of the toxicity of inhaled mineral dusts
-
Fubini, B. and Aräan, L.O. (1999) Chemical aspects of the toxicity of inhaled mineral dusts. Chem. Soc. Rev., 28, 373-382.
-
(1999)
Chem. Soc. Rev.
, vol.28
, pp. 373-382
-
-
Fubini, B.1
Aräan, L.O.2
-
2
-
-
0035886887
-
Enantioselective organocatalysis
-
Dalko, P.I. and Moisan, L. (2001) Enantioselective organocatalysis. Angew. Chem. Int. Ed., 40, 3726-3748.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 3726-3748
-
-
Dalko, P.I.1
Moisan, L.2
-
4
-
-
0141619399
-
Polymer-supported organic catalysts
-
Benaglia, M., Puglisi, A., and Cozzi, F. (2003) Polymer-supported organic catalysts. Chem. Rev., 103, 3401-3430.
-
(2003)
Chem. Rev.
, vol.103
, pp. 3401-3430
-
-
Benaglia, M.1
Puglisi, A.2
Cozzi, F.3
-
5
-
-
4143094833
-
Asymmetric organocatalysis
-
Special issue
-
(2004) Special issue: asymmetric organocatalysis. Acc. Chem. Res., 37, 487-631.
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 487-631
-
-
-
6
-
-
14744286984
-
-
Special issue
-
(2004) Special issue on organocatalysis. Adv. Synth. Catal., 346, 1007-1249.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 1007-1249
-
-
-
7
-
-
33645788277
-
-
Special issue
-
(2006) Special issue on organocatalysis. Tetrahedron, 62, 243-502.
-
(2006)
Tetrahedron
, vol.62
, pp. 243-502
-
-
-
8
-
-
38349142750
-
-
Special issue
-
(2007) Special issue on organocatalysis. Chem. Rev., 107, 5413-5883.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5413-5883
-
-
-
9
-
-
34547623607
-
Asymmetric organocatalysis
-
Pellissier, H. (2007) Asymmetric organocatalysis. Tetrahedron, 63, 9267-9331.
-
(2007)
Tetrahedron
, vol.63
, pp. 9267-9331
-
-
Pellissier, H.1
-
10
-
-
48849094479
-
Asymmetric organocatalysis: from infancy to adolescence
-
Dondoni, A. and Massi, A. (2008) Asymmetric organocatalysis: from infancy to adolescence. Angew. Chem. Int. Ed., 47, 4638-4660.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4638-4660
-
-
Dondoni, A.1
Massi, A.2
-
11
-
-
53549121402
-
Asymmetric aminocatalysis-Gold rush in organic chemistry
-
Melchiorre, P., Marigo, M., Carlone, A., and Bartoli, G. (2008) Asymmetric aminocatalysis-Gold rush in organic chemistry. Angew. Chem. Int. Ed., 47, 6138-6171.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6138-6171
-
-
Melchiorre, P.1
Marigo, M.2
Carlone, A.3
Bartoli, G.4
-
12
-
-
35348861428
-
Enantioselective direct aldol reaction: the blossoming of modern organocatalysis
-
Guillena, G., Nájera, C., and Ramón, D.J. (2007) Enantioselective direct aldol reaction: the blossoming of modern organocatalysis. Tetrahedron: Asymmetry, 18, 2249-2293.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2249-2293
-
-
Guillena, G.1
Nájera, C.2
Ramón, D.J.3
-
13
-
-
0034654216
-
Proline-catalyzed direct asymmetric aldol reactions
-
List, B., Lerner, R.A., and Barbas, C.F. III (2000) Proline-catalyzed direct asymmetric aldol reactions. J. Am. Chem. Soc., 122, 2395-2396.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 2395-2396
-
-
List, B.1
Lerner, R.A.2
Barbas III, C.F.3
-
14
-
-
84861495352
-
-
German Patent 2102 623. filled Jan. 21, 1970 and issued Jul. 29, 1971
-
Hajos, Z.G. and Parrish, D.R. (1971) Werkwijze voor de bereiding van 1,3-dioxycycloalkanen. German Patent 2102 623, filled Jan. 21, 1970 and issued Jul. 29, 1971.
-
(1971)
Werkwijze voor de bereiding van 1,3-dioxycycloalkanen
-
-
Hajos, Z.G.1
Parrish, D.R.2
-
16
-
-
33847804003
-
Asymmetric synthesis of bicyclic intermediates of natural product chemistry
-
Hajos, Z.G. and Parrish, D.R. (1974) Asymmetric synthesis of bicyclic intermediates of natural product chemistry. J. Org. Chem., 39, 1615-1621.
-
(1974)
J. Org. Chem.
, vol.39
, pp. 1615-1621
-
-
Hajos, Z.G.1
Parrish, D.R.2
-
17
-
-
84885768437
-
-
German Patent 2,014,757. filled Mar. 20, 1970 and issued Oct. 7, 1971
-
Eder, U., Sauer, G., and Wiechert, R. (1971) Verfahren zur herstellung optisch aktiver bicycloalkan derivate. German Patent 2,014,757, filled Mar. 20, 1970 and issued Oct. 7, 1971.
-
(1971)
Verfahren zur herstellung optisch aktiver bicycloalkan derivate
-
-
Eder, U.1
Sauer, G.2
Wiechert, R.3
-
18
-
-
84981886574
-
New type of asymmetric cyclization to optically active steroid cd partial structures
-
Eder, U., Sauer, G., and Wiechert, R. (1971) New type of asymmetric cyclization to optically active steroid cd partial structures. Angew. Chem. Int. Ed., 10, 496-497.
-
(1971)
Angew. Chem. Int. Ed.
, vol.10
, pp. 496-497
-
-
Eder, U.1
Sauer, G.2
Wiechert, R.3
-
19
-
-
0034600250
-
New strategies for organic catalysis: the first highly enantioselective organocatalytic Diels-Alder reaction
-
Ahrendt, K.A., Borths, C.J., and MacMillan, D.W.C. (2000) New strategies for organic catalysis: the first highly enantioselective organocatalytic Diels-Alder reaction. J. Am. Chem. Soc., 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
-
20
-
-
38349100690
-
Asymmetric enamine catalysis
-
Mukherjee, S., Woon Yang, Y., Hoffmann, S., and List, B. (2007) Asymmetric enamine catalysis. Chem. Rev., 107, 5471-5569.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Woon Yang, Y.2
Hoffmann, S.3
List, B.4
-
21
-
-
38349178582
-
Iminium catalysis
-
Erkkilä, A., Majander, I., and Pihko, P.M. (2007) Iminium catalysis. Chem. Rev., 107, 5416-5470.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5416-5470
-
-
Erkkilä, A.1
Majander, I.2
Pihko, P.M.3
-
22
-
-
43049134765
-
Advances in asymmetric organocatalytic reactions catalyzed by chiral primary amines
-
Peng, F. and Shao, Z. (2008) Advances in asymmetric organocatalytic reactions catalyzed by chiral primary amines. J. Mol. Catal. A: Chem., 285, 1-13.
-
(2008)
J. Mol. Catal. A: Chem.
, vol.285
, pp. 1-13
-
-
Peng, F.1
Shao, Z.2
-
23
-
-
49649083136
-
The development of asymmetric primary amine catalysts based on cinchona alkaloids
-
Chen, Y.-C. (2008) The development of asymmetric primary amine catalysts based on cinchona alkaloids. Synlett, 1919-1930.
-
(2008)
Synlett
, pp. 1919-1930
-
-
Chen, Y.-C.1
-
24
-
-
38349148300
-
Recent development and application of chiral phase-transfer catalysts
-
Hashimoto, T. and Maruoka, K. (2007) Recent development and application of chiral phase-transfer catalysts. Chem. Rev., 107, 5656-5682.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5656-5682
-
-
Hashimoto, T.1
Maruoka, K.2
-
25
-
-
38349189109
-
Stronger Brønsted acids
-
Akiyama, T. (2007) Stronger Brønsted acids. Chem. Rev., 107, 5744-5758.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5744-5758
-
-
Akiyama, T.1
-
26
-
-
38349135345
-
Small-molecule H-bond donors in asymmetric synthesis
-
Doyle, A.G. and Jacobsen, E.N. (2007) Small-molecule H-bond donors in asymmetric synthesis. Chem. Rev., 107, 5713-5743.
-
(2007)
Chem. Rev.
, vol.107
, pp. 5713-5743
-
-
Doyle, A.G.1
Jacobsen, E.N.2
-
28
-
-
0037043180
-
Proline-catalyzed asymmetric reactions
-
Review on proline-catalyzed reactions
-
Review on proline-catalyzed reactions: (a) List, B. (2002) Proline-catalyzed asymmetric reactions. Tetrahedron, 58, 5573-5590.
-
(2002)
Tetrahedron
, vol.58
, pp. 5573-5590
-
-
List, B.1
-
29
-
-
0037170944
-
Amino acids and peptides as asymmetric organocatalysts
-
Jarvo, E.R. and Miller, S.J. (2002) Amino acids and peptides as asymmetric organocatalysts. Tetrahedron, 58, 2481-2495.
-
(2002)
Tetrahedron
, vol.58
, pp. 2481-2495
-
-
Jarvo, E.R.1
Miller, S.J.2
-
30
-
-
4143114533
-
Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric aldol, Mannich, Michael, and Diels-Alder reactions
-
Notz, W., Tanaka, F., and Barbas, C.F. III (2004) Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric aldol, Mannich, Michael, and Diels-Alder reactions. Acc. Chem. Res., 37, 580-591.
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 580-591
-
-
Notz, W.1
Tanaka, F.2
Barbas III, C.F.3
-
31
-
-
0034812506
-
Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions
-
Selected recent examples on proline-catalyzed aldol reactions
-
Selected recent examples on proline-catalyzed aldol reactions: (a) Sakthivel, K., Notz, W., Bui, T., and Barbas, C.F. III (2001) Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. J. Am. Chem. Soc., 123, 5260-5267.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5260-5267
-
-
Sakthivel, K.1
Notz, W.2
Bui, T.3
Barbas III, C.F.4
-
32
-
-
33646508100
-
Dihydroxyacetone variants in the organocatalytic construction of carbohydrates: mimicking tagatose and fuculose aldolases
-
Suri, J.T., Mitsumori, S., Albertshofer, K., Tanaka, F., and Barbas, C.F. III (2006) Dihydroxyacetone variants in the organocatalytic construction of carbohydrates: mimicking tagatose and fuculose aldolases. J. Org. Chem., 71, 3822-3228.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 3822-3228
-
-
Suri, J.T.1
Mitsumori, S.2
Albertshofer, K.3
Tanaka, F.4
Barbas III, C.F.5
-
33
-
-
28944447661
-
Direct asymmetric organocatalytic de novo synthesis of carbohydrates
-
Grondal, C. and Enders, D. (2006) Direct asymmetric organocatalytic de novo synthesis of carbohydrates. Tetrahedron, 62, 329-337.
-
(2006)
Tetrahedron
, vol.62
, pp. 329-337
-
-
Grondal, C.1
Enders, D.2
-
34
-
-
17444375359
-
Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: a facile route to carbohydrates and aminosugars
-
Suri, J.T., Ramachary, D.B., and Barbas, C.F. III (2005) Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: a facile route to carbohydrates and aminosugars. Org. Lett., 7, 1383-1385.
-
(2005)
Org. Lett.
, vol.7
, pp. 1383-1385
-
-
Suri, J.T.1
Ramachary, D.B.2
Barbas III, C.F.3
-
35
-
-
17244373834
-
Amino acid catalyzed direct enantioselective formation of carbohydrates: one-step de novo synthesis of ketoses
-
Ibrahem, I. and Córdova, A. (2005) Amino acid catalyzed direct enantioselective formation of carbohydrates: one-step de novo synthesis of ketoses. Tetrahedron Lett., 46, 3363-3367.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3363-3367
-
-
Ibrahem, I.1
Córdova, A.2
-
36
-
-
3843118994
-
Enantioselective organocatalytic aldehyde-aldehyde cross-aldol couplings. The broad utility of a-thioacetal aldehydes
-
Storer, R.I. and MacMillan, D.W.C. (2004) Enantioselective organocatalytic aldehyde-aldehyde cross-aldol couplings. The broad utility of a-thioacetal aldehydes. Tetrahedron, 60, 7705-7714.
-
(2004)
Tetrahedron
, vol.60
, pp. 7705-7714
-
-
Storer, R.I.1
MacMillan, D.W.C.2
-
37
-
-
3142720242
-
Direct organocatalytic asymmetric α-hydroxymethylation of ketones and aldehydes
-
Casas, J., Sundén, H., and Córdova, A. (2004) Direct organocatalytic asymmetric α-hydroxymethylation of ketones and aldehydes. Tetrahedron Lett., 45, 6117-6119.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 6117-6119
-
-
Casas, J.1
Sundén, H.2
Córdova, A.3
-
38
-
-
1642528064
-
Diastereoselective aldol reaction of N,N-dibenzyl- α-amino aldehydes with ketones catalyzed by proline
-
Pan, Q., Zou, B., Wang, Y., and Ma, D. (2004) Diastereoselective aldol reaction of N,N-dibenzyl- α-amino aldehydes with ketones catalyzed by proline. Org. Lett., 6, 1009-1012.
-
(2004)
Org. Lett.
, vol.6
, pp. 1009-1012
-
-
Pan, Q.1
Zou, B.2
Wang, Y.3
Ma, D.4
-
39
-
-
3242806955
-
Enantioselective organocatalytic direct aldol reaction of α-oxylaldehydes: step one in a two-step synthesis of carbohydrates
-
Northrup, A.B., Mangion, I.K., Hettche, F., and MacMillan, D.W.C. (2004) Enantioselective organocatalytic direct aldol reaction of α-oxylaldehydes: step one in a two-step synthesis of carbohydrates. Angew. Chem. Int. Ed., 43, 2152-2154.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 2152-2154
-
-
Northrup, A.B.1
Mangion, I.K.2
Hettche, F.3
MacMillan, D.W.C.4
-
40
-
-
4143104623
-
Theory of asymmetric organocatalysis of aldol and related reactions: rationalizations and predictions
-
Allemann, C., Gordillo, R., Clemente, F.R., Cheong, P.H.-Y., and Houk, K.N. (2004) Theory of asymmetric organocatalysis of aldol and related reactions: rationalizations and predictions. Acc. Chem. Res., 37, 558-569.
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 558-569
-
-
Allemann, C.1
Gordillo, R.2
Clemente, F.R.3
Cheong, P.H.-Y.4
Houk, K.N.5
-
41
-
-
6444239481
-
Direct organocatalytic asymmetric aldol reactions of α-amino aldehydes: expedient syntheses of highly enantiomerically enriched anti-β-hydroxy-α-amino acids
-
Thayumanavan, R., Tanaka, F., and Barbas, C.F. III (2004) Direct organocatalytic asymmetric aldol reactions of α-amino aldehydes: expedient syntheses of highly enantiomerically enriched anti-β-hydroxy-α-amino acids. Org. Lett., 6, 3541-3544.
-
(2004)
Org. Lett.
, vol.6
, pp. 3541-3544
-
-
Thayumanavan, R.1
Tanaka, F.2
Barbas III, C.F.3
-
42
-
-
0038729533
-
Direct catalytic asymmetric enolexo aldolizations
-
Pidathala, C., Hoang, L., Vignola, N., and List, B. (2003) Direct catalytic asymmetric enolexo aldolizations. Angew. Chem. Int. Ed., 42, 2785-2788.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2785-2788
-
-
Pidathala, C.1
Hoang, L.2
Vignola, N.3
List, B.4
-
43
-
-
0034596452
-
A proline-catalyzed asymmetric Robinson annulation reaction
-
Bui, T. and Barbas, C.F. III (2000) A proline-catalyzed asymmetric Robinson annulation reaction. Tetrahedron Lett., 41, 6951-6954.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 6951-6954
-
-
Bui, T.1
Barbas III, C.F.2
-
44
-
-
0034721440
-
The direct catalytic asymmetric three-component Mannich reaction
-
List, B. (2000) The direct catalytic asymmetric three-component Mannich reaction. J. Am. Chem. Soc., 122, 9336.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9336
-
-
List, B.1
-
45
-
-
0037028924
-
A highly enantioselective amino acid-catalyzed route to functionalized α-amino acids
-
Córdova, A., Notz, W., Zhong, G., Betancort, J.M., and Barbas, C.F. III (2002) A highly enantioselective amino acid-catalyzed route to functionalized α-amino acids. J. Am. Chem. Soc., 124, 1842-1843.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1842-1843
-
-
Córdova, A.1
Notz, W.2
Zhong, G.3
Betancort, J.M.4
Barbas III, C.F.5
-
46
-
-
0037028550
-
The proline-catalyzed direct asymmetric three-component mannich reaction: scope, optimization, and application to the highly enantioselective synthesis of 1,2-amino alcohols
-
List, B., Pojarliev, P., Biller, W.T., and Martin, H.J. (2002) The proline-catalyzed direct asymmetric three-component mannich reaction: scope, optimization, and application to the highly enantioselective synthesis of 1,2-amino alcohols. J. Am. Chem. Soc., 124, 827-833.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 827-833
-
-
List, B.1
Pojarliev, P.2
Biller, W.T.3
Martin, H.J.4
-
47
-
-
0345529038
-
The direct organocatalytic asymmetric Mannich reaction: unmodified aldehydes as nucleophiles
-
Notz, W., Tanaka, F., Watanabe, S., Chowdari, N.S., Turner, J.M., Thayumanavan, R., and Barbas, C.F. III (2003) The direct organocatalytic asymmetric Mannich reaction: unmodified aldehydes as nucleophiles. J. Org. Chem., 68, 9624-9634.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 9624-9634
-
-
Notz, W.1
Tanaka, F.2
Watanabe, S.3
Chowdari, N.S.4
Turner, J.M.5
Thayumanavan, R.6
Barbas III, C.F.7
-
48
-
-
4043170073
-
Asymmetric synthesis of quaternary α- and β-amino acids and β-lactams via proline-catalyzed Mannich reactions with branched aldehyde donors
-
Chowdari, N.S., Suri, J.T., and Barbas, C.F. III (2004) Asymmetric synthesis of quaternary α- and β-amino acids and β-lactams via proline-catalyzed Mannich reactions with branched aldehyde donors. Org. Lett., 6, 2507-2510.
-
(2004)
Org. Lett.
, vol.6
, pp. 2507-2510
-
-
Chowdari, N.S.1
Suri, J.T.2
Barbas III, C.F.3
-
49
-
-
0042969372
-
The direct and enantioselective, one-pot, three-component, cross-Mannich reaction of aldehydes
-
Hayashi, Y., Tsuboi, W., Ashimine, I., Urushima, T., Shoji, M., and Sakai, K. (2003) The direct and enantioselective, one-pot, three-component, cross-Mannich reaction of aldehydes. Angew. Chem. Int. Ed., 42, 3677-3680.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3677-3680
-
-
Hayashi, Y.1
Tsuboi, W.2
Ashimine, I.3
Urushima, T.4
Shoji, M.5
Sakai, K.6
-
50
-
-
4243162724
-
Asymmetric tandem Mannich-Michael reaction
-
Córdova, A. (2003) Asymmetric tandem Mannich-Michael reaction. Synlett, 1651-1654.
-
(2003)
Synlett
, pp. 1651-1654
-
-
Córdova, A.1
-
51
-
-
0000761777
-
Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins
-
List, B., Pojarliev, P., and Martin, H.J. (2001) Efficient proline-catalyzed Michael additions of unmodified ketones to nitro olefins. Org. Lett., 3, 2423-2425.
-
(2001)
Org. Lett.
, vol.3
, pp. 2423-2425
-
-
List, B.1
Pojarliev, P.2
Martin, H.J.3
-
52
-
-
0035891780
-
Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors
-
Betancort, J.M. and Barbas, C.F. III (2001) Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors. Org. Lett., 3, 3737-3740.
-
(2001)
Org. Lett.
, vol.3
, pp. 3737-3740
-
-
Betancort, J.M.1
Barbas III, C.F.2
-
53
-
-
0036138062
-
Proline-catalyzed enantioselective Michael additions of ketones to nitrostyrene
-
Enders, D. and Seki, A. (2002) Proline-catalyzed enantioselective Michael additions of ketones to nitrostyrene. Synlett, 26-28.
-
(2002)
Synlett
, pp. 26-28
-
-
Enders, D.1
Seki, A.2
-
54
-
-
27644444355
-
Organocatalytic transformation of 1,3-diketones into optically active cyclohexanones
-
Gryko, D. (2005) Organocatalytic transformation of 1,3-diketones into optically active cyclohexanones. Tetrahedron: Asymmetry, 16, 1377-1383.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 1377-1383
-
-
Gryko, D.1
-
55
-
-
15744379986
-
Total synthesis of Brasoside and Littoralisone
-
Mangion, I.K. and MacMillan, D.W.C. (2005) Total synthesis of Brasoside and Littoralisone. J. Am. Chem. Soc., 127, 3696-3697.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3696-3697
-
-
Mangion, I.K.1
MacMillan, D.W.C.2
-
56
-
-
0036260164
-
Direct organo-catalytic asymmetric α-amination of aldehydes - a simple approach to optically active α-amino aldehydes, α-amino alcohols, and α-amino acids
-
Bøgevig, A., Juhl, K., Kumaragurubaran, N., Zhuang, W., and Jørgensen, K.A. (2002) Direct organo-catalytic asymmetric α-amination of aldehydes - a simple approach to optically active α-amino aldehydes, α-amino alcohols, and α-amino acids. Angew. Chem. Int. Ed., 41, 1790-1793.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1790-1793
-
-
Bøgevig, A.1
Juhl, K.2
Kumaragurubaran, N.3
Zhuang, W.4
Jørgensen, K.A.5
-
57
-
-
0037157154
-
Direct catalytic asymmetric α-amination of aldehydes
-
List, B. (2002) Direct catalytic asymmetric α-amination of aldehydes. J. Am. Chem. Soc., 124, 5656-5657.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 5656-5657
-
-
List, B.1
-
58
-
-
24944569764
-
Organocatalytic enantioselective synthesis of metabotropic glutamate receptor ligands
-
Suri, J.T., Steiner, D.D., and Barbas, C.F. III (2005) Organocatalytic enantioselective synthesis of metabotropic glutamate receptor ligands. Org. Lett., 7, 3885-3888.
-
(2005)
Org. Lett.
, vol.7
, pp. 3885-3888
-
-
Suri, J.T.1
Steiner, D.D.2
Barbas III, C.F.3
-
59
-
-
24644515890
-
First examples of proline-catalyzed domino Knoevenagel/hetero-Diels-Alder/ elimination reactions
-
Sabitha, G., Fatima, N., Reddy, E.V., and Yadav, J.S. (2005) First examples of proline-catalyzed domino Knoevenagel/hetero-Diels-Alder/ elimination reactions. Adv. Synth. Catal., 347, 1353-1355.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1353-1355
-
-
Sabitha, G.1
Fatima, N.2
Reddy, E.V.3
Yadav, J.S.4
-
60
-
-
0037140856
-
Amine-catalyzed direct Diels-Alder reactions of α' β-unsaturated ketones with nitro olefins
-
Thayumanavan, R., Dhevalapally, B., Sakthivel, K., Tanaka, F., and Barbas, C.F. III (2002) Amine-catalyzed direct Diels-Alder reactions of α' β-unsaturated ketones with nitro olefins. Tetrahedron Lett., 43, 3817-3820.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3817-3820
-
-
Thayumanavan, R.1
Dhevalapally, B.2
Sakthivel, K.3
Tanaka, F.4
Barbas III, C.F.5
-
61
-
-
0037119742
-
Amine-catalyzed direct self Diels-Alder reactions of a β-unsaturated ketones in water: synthesis of pro-chiral cyclohexanes
-
Ramachary, D.B., Chowdari, N.S., and Barbas, C.F. III (2002) Amine-catalyzed direct self Diels-Alder reactions of a β-unsaturated ketones in water: synthesis of pro-chiral cyclohexanes. Tetrahedron Lett., 43, 6743-6746.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6743-6746
-
-
Ramachary, D.B.1
Chowdari, N.S.2
Barbas III, C.F.3
-
62
-
-
0036134467
-
Lewis base and l-proline co-catalyzed Baylis- Hillman reaction of arylaldehydes with methyl vinyl ketone
-
Shi, M., Jiang, J.K., and Li, C.Q. (2002) Lewis base and l-proline co-catalyzed Baylis- Hillman reaction of arylaldehydes with methyl vinyl ketone. Tetrahedron Lett., 43, 127-130.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 127-130
-
-
Shi, M.1
Jiang, J.K.2
Li, C.Q.3
-
63
-
-
27944479071
-
An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis- Hillman reaction
-
Chen, S.H., Hong, B.C., Su, C.F., and Sarshar, S. (2005) An unexpected inversion of enantioselectivity in the proline catalyzed intramolecular Baylis- Hillman reaction. Tetrahedron Lett., 46, 8899-8903.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 8899-8903
-
-
Chen, S.H.1
Hong, B.C.2
Su, C.F.3
Sarshar, S.4
-
64
-
-
0142042898
-
Dual catalyst control in the amino acid-peptide-catalyzed enantioselective Baylis-Hillman reaction
-
Imbriglio, J.E., Vasbinder, M.M., and Miller, S.J. (2003) Dual catalyst control in the amino acid-peptide-catalyzed enantioselective Baylis-Hillman reaction. Org. Lett., 5, 3741-3743.
-
(2003)
Org. Lett.
, vol.5
, pp. 3741-3743
-
-
Imbriglio, J.E.1
Vasbinder, M.M.2
Miller, S.J.3
-
65
-
-
34249712553
-
A way to highly enantiomerically enriched aza-Morita-Baylis-Hillman-type products
-
Utsumi, N., Zhang, H., Tanaka, F., and Barbas, C.F. III (2007) A way to highly enantiomerically enriched aza-Morita-Baylis-Hillman-type products. Angew. Chem. Int. Ed., 46, 1878-1880.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 1878-1880
-
-
Utsumi, N.1
Zhang, H.2
Tanaka, F.3
Barbas III, C.F.4
-
66
-
-
34548249167
-
Aza-Morita-Baylis-Hillman-type reactions : highly enantioselective organocatalytic addition of unmodified α, β-unsaturated aldehydes to N-Boc protected imines
-
Vesely, J., Dziedzic, P., and Córdova, A. (2007) Aza-Morita-Baylis-Hillman-type reactions : highly enantioselective organocatalytic addition of unmodified α, β-unsaturated aldehydes to N-Boc protected imines. Tetrahedron Lett., 48, 6900-6904.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 6900-6904
-
-
Vesely, J.1
Dziedzic, P.2
Córdova, A.3
-
67
-
-
84961985214
-
Direct, facile aldehyde and ketone α-selenenylation reactions promoted by l-prolinamide and pyrrolidine sulfonamide organocatalysts
-
Wang, J., Li, H., Mei, Y., Lou, B., Xu, D., Xie, D., Guo, H., and Wang, W. (2005) Direct, facile aldehyde and ketone α-selenenylation reactions promoted by l-prolinamide and pyrrolidine sulfonamide organocatalysts. J. Org. Chem., 70, 5678-5687.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 5678-5687
-
-
Wang, J.1
Li, H.2
Mei, Y.3
Lou, B.4
Xu, D.5
Xie, D.6
Guo, H.7
Wang, W.8
-
68
-
-
0141522552
-
A facile and rapid route to highly enantiopure 1,2-diols by novel catalytic asymmetric -aminoxylation of aldehydes
-
Zhong, G. (2003) A facile and rapid route to highly enantiopure 1,2-diols by novel catalytic asymmetric -aminoxylation of aldehydes. Angew. Chem. Int. Ed., 42, 4247-4250.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 4247-4250
-
-
Zhong, G.1
-
69
-
-
0041733541
-
The direct and enantioselective organocatalytic α-oxidation of aldehydes
-
Brown, S.P., Brochu, M.P., Sinz, C.J., and MacMillan, D.W.C. (2003) The direct and enantioselective organocatalytic α-oxidation of aldehydes. J. Am. Chem. Soc., 125, 10808-10809.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10808-10809
-
-
Brown, S.P.1
Brochu, M.P.2
Sinz, C.J.3
MacMillan, D.W.C.4
-
70
-
-
0141957357
-
Direct proline catalyzed asymmetric α-aminooxylation of aldehydes
-
Hayashi, Y., Yamaguchi, J., Hibino, K., and Shoji, M. (2003) Direct proline catalyzed asymmetric α-aminooxylation of aldehydes. Tetrahedron Lett., 44, 8293-8296.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 8293-8296
-
-
Hayashi, Y.1
Yamaguchi, J.2
Hibino, K.3
Shoji, M.4
-
71
-
-
1842792133
-
Direct catalytic enantioselective -aminoxylation of ketones: a stereoselective synthesis of α-hydroxy and α' α' -dihydroxy ketones
-
Bøgevig, A., Sundén, H., and Córdova, A. (2004) Direct catalytic enantioselective -aminoxylation of ketones: a stereoselective synthesis of α-hydroxy and α' α' -dihydroxy ketones. Angew. Chem. Int. Ed., 43, 1109-1112.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 1109-1112
-
-
Bøgevig, A.1
Sundén, H.2
Córdova, A.3
-
72
-
-
4243057730
-
Direct proline-catalyzed asymmetric α-aminoxylation of ketones
-
Hayashi, Y., Yamaguchi, J., Hibino, K., and Shoji, M. (2004) Direct proline-catalyzed asymmetric α-aminoxylation of ketones. Angew. Chem. Int. Ed., 43, 1112-1115.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 1112-1115
-
-
Hayashi, Y.1
Yamaguchi, J.2
Hibino, K.3
Shoji, M.4
-
73
-
-
4344693780
-
Direct proline-catalyzed asymmetric α-aminoxylation of aldehydes and ketones
-
Hayashi, Y., Yamaguchi, J., Sumiya, T., Hibino, K., and Shoji, M. (2004) Direct proline-catalyzed asymmetric α-aminoxylation of aldehydes and ketones. J. Org. Chem., 69, 5966-5973.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 5966-5973
-
-
Hayashi, Y.1
Yamaguchi, J.2
Sumiya, T.3
Hibino, K.4
Shoji, M.5
-
74
-
-
4243126802
-
The direct catalytic asymmetric α-aminooxylation reaction: development of stereoselective routes to 1,2-diols and 1,2-amino alcohols and density functional calculations
-
Córdova, A., Sundén, H., Bøgevig, A., Johansson, M., and Himo, F. (2004) The direct catalytic asymmetric α-aminooxylation reaction: development of stereoselective routes to 1,2-diols and 1,2-amino alcohols and density functional calculations. Chem. Eur. J., 10, 3673-3684.
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 3673-3684
-
-
Córdova, A.1
Sundén, H.2
Bøgevig, A.3
Johansson, M.4
Himo, F.5
-
75
-
-
1842450587
-
Direct and enantioselective organocatalytic α-chlorination of aldehydes
-
Brochu, M.P., Brown, S.P., and MacMillan, D.W.C. (2004) Direct and enantioselective organocatalytic α-chlorination of aldehydes. J. Am. Chem. Soc., 126, 4108-4109.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4108-4109
-
-
Brochu, M.P.1
Brown, S.P.2
MacMillan, D.W.C.3
-
76
-
-
0026733927
-
Asymmetric syntheses with chiral oxazaborolidines
-
Wallbaum, S. and Martens, J. (1992) Asymmetric syntheses with chiral oxazaborolidines. Tetrahedron: Asymmetry, 3, 1475-1504.
-
(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 1475-1504
-
-
Wallbaum, S.1
Martens, J.2
-
77
-
-
0028968254
-
Catalytic enantioselective allylic oxidation
-
Rispens, M.T., Zondervan, C., and Feringa, B.L. (1995) Catalytic enantioselective allylic oxidation. Tetrahedron: Asymmetry, 6, 661-664.
-
(1995)
Tetrahedron: Asymmetry
, vol.6
, pp. 661-664
-
-
Rispens, M.T.1
Zondervan, C.2
Feringa, B.L.3
-
78
-
-
0034807741
-
New strategies in organic catalysis: the first enantioselective organocatalytic Friedel-Crafts alkylation
-
Para, N.A. and MacMillan, D.W.C. (2001) New strategies in organic catalysis: the first enantioselective organocatalytic Friedel-Crafts alkylation. J. Am. Chem. Soc., 123, 4370-4371.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 4370-4371
-
-
Para, N.A.1
MacMillan, D.W.C.2
-
79
-
-
34247565955
-
Enantioselective organocatalysis using SOMO activation
-
Beeson, T.D., Mastracchio, A., Hong, J.-B., Ashton, K., and MacMillan, D.W.C. (2007) Enantioselective organocatalysis using SOMO activation. Science, 316, 582-585.
-
(2007)
Science
, vol.316
, pp. 582-585
-
-
Beeson, T.D.1
Mastracchio, A.2
Hong, J.-B.3
Ashton, K.4
MacMillan, D.W.C.5
-
80
-
-
40149110106
-
Enantioselective organo-SOMO catalysis: the α-vinylation of aldehydes
-
Kim, H. and MacMillan, D.W.C. (2007) Enantioselective organo-SOMO catalysis: the α-vinylation of aldehydes. J. Am. Chem. Soc., 130, 398-399.
-
(2007)
J. Am. Chem. Soc.
, vol.130
, pp. 398-399
-
-
Kim, H.1
MacMillan, D.W.C.2
-
81
-
-
47749137879
-
Supported proline and proline-derivatives as recyclable organocatalysts
-
Gruttadauria, M., Giacalone, F., and Noto, R. (2008) Supported proline and proline-derivatives as recyclable organocatalysts. Chem. Soc. Rev., 37, 1666-1688.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1666-1688
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
82
-
-
58549093369
-
Water in stereoselective organocatalytic reactions
-
Gruttadauria, M., Giacalone, F., and Noto, R. (2009) Water in stereoselective organocatalytic reactions. Adv. Synth. Catal., 351, 33-57.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 33-57
-
-
Gruttadauria, M.1
Giacalone, F.2
Noto, R.3
-
83
-
-
0033575414
-
The unexpected and the unpredictable in organic synthesis
-
Mukaiyama, T. (1999) The unexpected and the unpredictable in organic synthesis. Tetrahedron, 55, 8609-8670.
-
(1999)
Tetrahedron
, vol.55
, pp. 8609-8670
-
-
Mukaiyama, T.1
-
84
-
-
0002979399
-
The art and science of total synthesis at the dawn of the twenty-first century
-
Nicolaou, K.C., Vourloumis, D., Wissinger, N., and Baran, P.S. (2000) The art and science of total synthesis at the dawn of the twenty-first century. Angew. Chem. Int. Ed., 39, 44-122.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 44-122
-
-
Nicolaou, K.C.1
Vourloumis, D.2
Wissinger, N.3
Baran, P.S.4
-
85
-
-
0028937415
-
Total synthesis of the polyether antibiotic Lonomycin A (Emericid)
-
Evans, D.A., Ratz, A.M.B., Huff, E., and Sheppard, G.S. (1995) Total synthesis of the polyether antibiotic Lonomycin A (Emericid). J. Am. Chem. Soc., 117, 3448-3467.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3448-3467
-
-
Evans, D.A.1
Ratz, A.M.B.2
Huff, E.3
Sheppard, G.S.4
-
86
-
-
0000425224
-
Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelates
-
Narasaka, K. and Pai, F.-C. (1984) Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelates. Tetrahedron, 40, 2233-2238.
-
(1984)
Tetrahedron
, vol.40
, pp. 2233-2238
-
-
Narasaka, K.1
Pai, F.-C.2
-
87
-
-
0033515504
-
An especially convenient stereoselective reduction of β-hydroxy ketones to anti 1,3 diols using samarium diiodide
-
Keck, G.E., Wager, C.A., Sell, T., and Wager, T.T. (1999) An especially convenient stereoselective reduction of β-hydroxy ketones to anti 1,3 diols using samarium diiodide. J. Org. Chem., 64, 2172-2173.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2172-2173
-
-
Keck, G.E.1
Wager, C.A.2
Sell, T.3
Wager, T.T.4
-
89
-
-
0037463084
-
The direct catalytic asymmetric cross-aldol reaction of aldehydes
-
Alcaide, B. and Almendros, P. (2003) The direct catalytic asymmetric cross-aldol reaction of aldehydes. Angew. Chem. Int. Ed., 42, 858-860.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 858-860
-
-
Alcaide, B.1
Almendros, P.2
-
90
-
-
0037016618
-
The aldol addition reaction: an old transformation at constant rebirth
-
Palomo, C., Oiarbide, M., and Garcia, J.M. (2002) The aldol addition reaction: an old transformation at constant rebirth. Chem. Eur. J., 8, 36.
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 36
-
-
Palomo, C.1
Oiarbide, M.2
Garcia, J.M.3
-
91
-
-
11844259698
-
-
vols. 1, 2, Wiley-VCH Verlag GmbH, Weinheim
-
Mahrwald, R. (ed.) (2004) Modern Aldol Reactions, vols. 1, 2, Wiley-VCH Verlag GmbH, Weinheim.
-
(2004)
Modern Aldol Reactions
-
-
Mahrwald, R.1
-
92
-
-
0029109703
-
Enzymes in organic synthesis: application to the problems of carbohydrate recognition
-
Wong, C.-H., Halcomb, R.L., Ichikawa, Y., and Kajimoto, T. (1995) Enzymes in organic synthesis: application to the problems of carbohydrate recognition. Angew. Chem. Int. Ed. Engl., 34, 412-432.
-
(1995)
Angew. Chem. Int. Ed. Engl.
, vol.34
, pp. 412-432
-
-
Wong, C.-H.1
Halcomb, R.L.2
Ichikawa, Y.3
Kajimoto, T.4
-
93
-
-
0347417134
-
Room-temperature ionic liquids. Solvents for synthesis and catalysis
-
Welton, T. (1999) Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chem. Rev., 99, 2071-2083.
-
(1999)
Chem. Rev.
, vol.99
, pp. 2071-2083
-
-
Welton, T.1
-
94
-
-
0037092828
-
Ionic liquids: applications in catalysis
-
Zhao, D., Wu, M., Kou, Y., and Min, E. (2002) Ionic liquids: applications in catalysis. Catal. Today, 74, 157-189.
-
(2002)
Catal. Today
, vol.74
, pp. 157-189
-
-
Zhao, D.1
Wu, M.2
Kou, Y.3
Min, E.4
-
95
-
-
0036979260
-
Proline-catalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6
-
Kotrusz, P., Kmentová, I., Gotov, B., Toma, S., and Solčaniová, E. (2002) Proline-catalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6. Chem. Commun., 2510-2511.
-
(2002)
Chem. Commun.
, pp. 2510-2511
-
-
Kotrusz, P.1
Kmentová, I.2
Gotov, B.3
Toma, S.4
Solčaniová, E.5
-
96
-
-
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., and Yang, J.-Y. (2002) l-Proline in an ionic liquid as an efficient and reusable catalyst for direct asymmetric aldol reactions. Tetrahedron Lett., 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
-
97
-
-
1942467938
-
Direct catalytic asymmetric cross-aldol reactions in ionic liquid media
-
Córdova, A. (2004) Direct catalytic asymmetric cross-aldol reactions in ionic liquid media. Tetrahedron Lett., 45, 3949-3952.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 3949-3952
-
-
Córdova, A.1
-
98
-
-
33748281160
-
Ionic-liquid-supported organocatalyst: efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction
-
Miao, W. and Chan, T.H. (2006) Ionic-liquid-supported organocatalyst: efficient and recyclable ionic-liquid-anchored proline for asymmetric aldol reaction. Adv. Synth. Catal., 348, 1711-1718.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 1711-1718
-
-
Miao, W.1
Chan, T.H.2
-
99
-
-
33746216402
-
Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins
-
Luo, S., Mi, X., Zhang, L., Liu, S., Xu, H., and Cheng, J.-P. (2006) Functionalized chiral ionic liquids as highly efficient asymmetric organocatalysts for Michael addition to nitroolefins. Angew. Chem. Int. Ed., 45, 3093-3097.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3093-3097
-
-
Luo, S.1
Mi, X.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.-P.6
-
100
-
-
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., and Trombini, C. (2007) An improved protocol for the direct asymmetric aldol reaction in ionic liquids, catalysed by onium ion-tagged prolines. Adv. Synth. Catal., 349, 2061-2065.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2061-2065
-
-
Lombardo, M.1
Pasi, F.2
Easwar, S.3
Trombini, C.4
-
101
-
-
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., and Zlotin, S.G. (2008) A novel (S)-proline-modified task-specific chiral ionic liquid - an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water. Tetrahedron Lett., 49, 1212-1216.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1212-1216
-
-
Siyutkin, D.E.1
Kucherenko, A.S.2
Struchkova, M.I.3
Zlotin, S.G.4
-
102
-
-
0037032306
-
Supported ionic liquid catalysis - a new concept for homogeneous hydroformylation catalysis
-
Mehnert, C.P., Cook, R.A., Dispenziere, N.C., and Afeworki, M. (2002) Supported ionic liquid catalysis - a new concept for homogeneous hydroformylation catalysis. J. Am. Chem. Soc., 124, 12932-12933.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 12932-12933
-
-
Mehnert, C.P.1
Cook, R.A.2
Dispenziere, N.C.3
Afeworki, M.4
-
103
-
-
14744285043
-
Supported ionic liquid catalysis
-
Mehnert, C.P. (2005) Supported ionic liquid catalysis. Chem. Eur. J., 11, 50-56.
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 50-56
-
-
Mehnert, C.P.1
-
104
-
-
3142751057
-
Supported ionic liquid asymmetric catalysis. A new method for chiral catalysts recycling. the case of proline-catalyzed aldol reaction
-
Gruttadauria, M., Riela, S., Lo Meo, P., D'Anna, F., and Noto, R. (2004) Supported ionic liquid asymmetric catalysis. a new method for chiral catalysts recycling. the case of proline-catalyzed aldol reaction. Tetrahedron Lett., 45, 6113-6116.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 6113-6116
-
-
Gruttadauria, M.1
Riela, S.2
Lo Meo, P.3
D'Anna, F.4
Noto, R.5
-
105
-
-
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., and Noto, R. (2006) Supported ionic liquids. New recyclable materials for the l-proline-catalyzed aldol reaction. Adv. Synth. Catal., 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
-
106
-
-
18244393987
-
Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions
-
Krattiger, P., Kovasy, R., Revell, J.D., Ivan, S., and Wennemers, H. (2005) Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions. Org. Lett., 7, 1101-1103.
-
(2005)
Org. Lett.
, vol.7
, pp. 1101-1103
-
-
Krattiger, P.1
Kovasy, R.2
Revell, J.D.3
Ivan, S.4
Wennemers, H.5
-
107
-
-
36349032715
-
New ionic liquid-modified silica gels as recyclable materials for l-prolineor H-Pro- Pro-Asp-NH2-catalyzed aldol reaction
-
Aprile, C., Giacalone, F., Gruttadauria, M., Mossuto Marculescu, A., Noto, R., Revell, J.D., and Wennemers, H. (2007) New ionic liquid-modified silica gels as recyclable materials for l-prolineor H-Pro- Pro-Asp-NH2-catalyzed aldol reaction. Green Chem., 9, 1328-1334.
-
(2007)
Green Chem.
, vol.9
, pp. 1328-1334
-
-
Aprile, C.1
Giacalone, F.2
Gruttadauria, M.3
Mossuto Marculescu, A.4
Noto, R.5
Revell, J.D.6
Wennemers, H.7
-
108
-
-
0000776283
-
Enantioselective aldol condensations catalyzed by poly(ethylene glycol)-supported proline
-
Benaglia, M., Celentano, G., and Cozzi, F. (2001) Enantioselective aldol condensations catalyzed by poly(ethylene glycol)-supported proline. Adv. Synth. Catal., 343, 171-173.
-
(2001)
Adv. Synth. Catal.
, vol.343
, pp. 171-173
-
-
Benaglia, M.1
Celentano, G.2
Cozzi, F.3
-
109
-
-
0001682147
-
Poly(ethylene glycol)-supported proline: a versatile catalyst for the enantioselective aldol and iminoaldol reactions
-
Benaglia, M., Cinquini, M., Cozzi, F., Puglisi, A., and Celentano, G. (2002) Poly(ethylene glycol)-supported proline: a versatile catalyst for the enantioselective aldol and iminoaldol reactions. Adv. Synth. Catal., 344, 533-542.
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 533-542
-
-
Benaglia, M.1
Cinquini, M.2
Cozzi, F.3
Puglisi, A.4
Celentano, G.5
-
110
-
-
18744419145
-
Poly(ethylene-glycol)-supported proline: a recyclable aminocatalyst for the enantioselective synthesis of γ -nitroketones by conjugate addition
-
Benaglia, M., Cinquini, M., Cozzi, F., Puglisi, A., and Celentano, G. (2003) Poly(ethylene-glycol)-supported proline: a recyclable aminocatalyst for the enantioselective synthesis of γ -nitroketones by conjugate addition. J. Mol. Catal. A: Chem., 204-205, 157-163.
-
(2003)
J. Mol. Catal. A: Chem.
, vol.204-205
, pp. 157-163
-
-
Benaglia, M.1
Cinquini, M.2
Cozzi, F.3
Puglisi, A.4
Celentano, G.5
-
111
-
-
33846632873
-
A new class of efficient poly(ethylene-glycol)-supported catalyst based on proline for the asymmetric Michael addition of ketones to nitrostyrenes
-
Gu, L., Wu, Y., Zhang, Y., and Zhao, G. (2007) A new class of efficient poly(ethylene-glycol)-supported catalyst based on proline for the asymmetric Michael addition of ketones to nitrostyrenes. J. Mol. Catal. A: Chem., 263, 186-194.
-
(2007)
J. Mol. Catal. A: Chem.
, vol.263
, pp. 186-194
-
-
Gu, L.1
Wu, Y.2
Zhang, Y.3
Zhao, G.4
-
112
-
-
33750070045
-
Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water
-
Font, D., Jimeno, C., and Pericàs, M.A. (2006) Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water. Org. Lett., 8, 4653-4656.
-
(2006)
Org. Lett.
, vol.8
, pp. 4653-4656
-
-
Font, D.1
Jimeno, C.2
Pericàs, M.A.3
-
113
-
-
38749143339
-
Toward an artificial aldolase. M. A. Pericàs
-
Font, D., Sayalero, S., Bastero, A., and Jimeno, C. (2008) Toward an artificial aldolase. M. A. Pericàs. Org. Lett., 10, 337-340.
-
(2008)
Org. Lett.
, vol.10
, pp. 337-340
-
-
Font, D.1
Sayalero, S.2
Bastero, A.3
Jimeno, C.4
-
114
-
-
34249297939
-
Highly enantioselective α-aminoxylation of aldehydes and ketones with a polymer-supported organocatalyst
-
Font, D., Bastero, A., Sayalero, S., Jimeno, C., and Pericàs, M.A. (2007) Highly enantioselective α-aminoxylation of aldehydes and ketones with a polymer-supported organocatalyst. Org. Lett., 9, 1943-1946.
-
(2007)
Org. Lett.
, vol.9
, pp. 1943-1946
-
-
Font, D.1
Bastero, A.2
Sayalero, S.3
Jimeno, C.4
Pericàs, M.A.5
-
115
-
-
24644508440
-
Asymmetric aldol reaction using immobilized proline on mesoporous support
-
Calderón, F., Fernández, R., Sánchez, F., and Fernández-Mayoralas, A. (2005) Asymmetric aldol reaction using immobilized proline on mesoporous support. Adv. Synth. Catal., 347, 1395-1403.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1395-1403
-
-
Calderón, F.1
Fernández, R.2
Sánchez, F.3
Fernández-Mayoralas, A.4
-
116
-
-
36649037581
-
Asymmetric aldol reaction catalyzed by a heterogenized proline on a mesoporous support. The role of the nature of solvents
-
Doyag̈uez, E.G., Calderón, F., Fernández, R., Sánchez, F., and Fernández-Mayoralas, A. (2007) Asymmetric aldol reaction catalyzed by a heterogenized proline on a mesoporous support. The role of the nature of solvents. J. Org. Chem., 72, 9353-9356.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 9353-9356
-
-
Doyag̈uez, E.G.1
Calderón, F.2
Fernández, R.3
Sánchez, F.4
Fernández-Mayoralas, A.5
-
117
-
-
36248978276
-
Magnetic nanoparticle-supported proline as a recyclable and recoverable ligand for the CuI catalyzed arylation of nitrogen nucleophiles
-
Chouhan, G., Wang, D., and Alper, H. (2007) Magnetic nanoparticle-supported proline as a recyclable and recoverable ligand for the CuI catalyzed arylation of nitrogen nucleophiles. Chem. Commun., 4809-4810.
-
(2007)
Chem. Commun.
, pp. 4809-4810
-
-
Chouhan, G.1
Wang, D.2
Alper, H.3
-
118
-
-
33845336873
-
Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and α-selenenylation of aldehydes
-
Giacalone, F., Gruttadauria, M., Mossuto Marculescu, A., and Noto, R. (2007) Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and α-selenenylation of aldehydes. Tetrahedron Lett., 48, 255-259.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 255-259
-
-
Giacalone, F.1
Gruttadauria, M.2
Mossuto Marculescu, A.3
Noto, R.4
-
122
-
-
0002389988
-
Functional group manipulation using organoselenium reagents
-
Reich, H.J. (1979) Functional group manipulation using organoselenium reagents. Acc. Chem. Res., 12, 22-30.
-
(1979)
Acc. Chem. Res.
, vol.12
, pp. 22-30
-
-
Reich, H.J.1
-
123
-
-
84867228113
-
-
US Patent 3,743,669, filed Nov. 6, 1970 and issued Jul. 3, 1973
-
Hillman, M.E.D. and Baylis, A.B. (1973) Reaction of acrylic type compounds with aldehydes and certain ketones. US Patent 3,743,669, filed Nov. 6, 1970 and issued Jul. 3, 1973.
-
(1973)
Reaction of acrylic type compounds with aldehydes and certain ketones
-
-
Hillman, M.E.D.1
Baylis, A.B.2
-
124
-
-
0037366617
-
Recent advances in the Baylis-Hillman reaction and applications
-
Basavaiah, D., Jaganmohan Rao, A., and Satyanarayana, T. (2003) Recent advances in the Baylis-Hillman reaction and applications. Chem. Rev., 103, 811-892.
-
(2003)
Chem. Rev.
, vol.103
, pp. 811-892
-
-
Basavaiah, D.1
Jaganmohan Rao, A.2
Satyanarayana, T.3
-
125
-
-
34548185871
-
The Baylis- Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry
-
Basavaiah, D., Venkateswara Rao, K., and Jannapu Reddy, R. (2007) The Baylis- Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry. Chem. Soc. Rev., 36, 1581-1588.
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1581-1588
-
-
Basavaiah, D.1
Venkateswara Rao, K.2
Jannapu Reddy, R.3
-
126
-
-
0036134467
-
Lewis base and l-proline co-catalyzed Baylis- Hillman reaction of arylaldehydes with methyl vinyl ketone
-
Shi, M., Jiang, J.-K., and Li, C.-Q. (2002) Lewis base and l-proline co-catalyzed Baylis- Hillman reaction of arylaldehydes with methyl vinyl ketone. Tetrahedron Lett., 43, 127-130.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 127-130
-
-
Shi, M.1
Jiang, J.-K.2
Li, C.-Q.3
-
127
-
-
33846347896
-
Aminocatalysis of the Baylis- Hillman reaction: an important solvent effect
-
Davies, A.H.J., Ruda, M., and Tomkinson, N.C.O. (2007) Aminocatalysis of the Baylis- Hillman reaction: an important solvent effect. Tetrahedron Lett., 48, 1461-1464.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 1461-1464
-
-
Davies, A.H.J.1
Ruda, M.2
Tomkinson, N.C.O.3
-
128
-
-
0345393093
-
Heterogeneous Baylis- Hillman using a polystyrene-bound 4-(N-benzyl-N-methylamino)pyridine as reusable catalyst
-
Corma, A., García, H., and Leyva, A. (2003) Heterogeneous Baylis- Hillman using a polystyrene-bound 4-(N-benzyl-N-methylamino)pyridine as reusable catalyst. Chem. Commun., 2806-2807.
-
(2003)
Chem. Commun.
, pp. 2806-2807
-
-
Corma, A.1
García, H.2
Leyva, A.3
-
129
-
-
25444501833
-
Dialkylaminopyridine-functionalized Mesoporous Silica nanosphere as an efficient and highly stable heterogeneous nucleophilic catalyst
-
Chen, H.-T., Huh, S., Wiench, J.W., Pruski, M., and Lin, V.S.-Y. (2005) Dialkylaminopyridine-functionalized Mesoporous Silica nanosphere as an efficient and highly stable heterogeneous nucleophilic catalyst. J. Am. Chem. Soc., 127, 13305-13311.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13305-13311
-
-
Chen, H.-T.1
Huh, S.2
Wiench, J.W.3
Pruski, M.4
Lin, V.S.-Y.5
-
130
-
-
26844556203
-
One-pot reaction cascades using star polymers with core-confined catalysts
-
Helms, B., Guillaudeu, S.J., Xie, Y., McMurdo, M., Hawker, C.J., and Fréchet, J.M.J. (2005) One-pot reaction cascades using star polymers with core-confined catalysts. Angew. Chem. Int. Ed., 44, 6384.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6384
-
-
Helms, B.1
Guillaudeu, S.J.2
Xie, Y.3
McMurdo, M.4
Hawker, C.J.5
Fréchet, J.M.J.6
-
131
-
-
39549100133
-
Polystyrene-supported proline as recyclable catalyst in the Baylis-Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone
-
Giacalone, F., Gruttadauria, M., Mossuto Marculescu, A., D'Anna, F., and Noto, R. (2008) Polystyrene-supported proline as recyclable catalyst in the Baylis-Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone. Catal. Commun., 9, 1477-1481.
-
(2008)
Catal. Commun.
, vol.9
, pp. 1477-1481
-
-
Giacalone, F.1
Gruttadauria, M.2
Mossuto Marculescu, A.3
D'Anna, F.4
Noto, R.5
-
132
-
-
0036927410
-
Direct organocatalytic aldol reactions in buffered aqueous media
-
Cordova, A., Notz, W., and Barbas, C.F. III (2002) Direct organocatalytic aldol reactions in buffered aqueous media. Chem. Commun., 3024.
-
(2002)
Chem. Commun.
, pp. 3024
-
-
Cordova, A.1
Notz, W.2
Barbas III, C.F.3
-
133
-
-
31444456557
-
Organocatalytic direct asymmetric aldol reactions in water
-
Mase, N., Nakai, Y., Ohara, N., Yoda, H., Takabe, K., Tanaka, F., and Barbas, C.F. III (2006) Organocatalytic direct asymmetric aldol reactions in water. J. Am. Chem. Soc., 128, 734-735.
-
(2006)
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 III, C.F.7
-
134
-
-
32044463187
-
Highly diastereo- and enantioselective direct aldol reactions in water
-
Hayashi, Y., Sumiya, T., Takahashi, J., Gotoh, H., Urushima, T., and Shoji, M. (2006) Highly diastereo- and enantioselective direct aldol reactions in water. Angew. Chem. Int. Ed., 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
-
135
-
-
35348857641
-
Hydrophobically directed aldol reactions: polystyrene-supported l-proline as recyclable catalyst for direct asymmetric aldol reaction in the presence of water
-
Gruttadauria, M., Giacalone, F., Mossuto Marculescu, A., Lo Meo, P., Riela, S., and Noto, R. (2007) Hydrophobically directed aldol reactions: polystyrene-supported l-proline as recyclable catalyst for direct asymmetric aldol reaction in the presence of water. Eur. J. Org. Chem., 4688-4698.
-
(2007)
Eur. J. Org. Chem.
, pp. 4688-4698
-
-
Gruttadauria, M.1
Giacalone, F.2
Mossuto Marculescu, A.3
Lo Meo, P.4
Riela, S.5
Noto, R.6
-
136
-
-
33748926253
-
Highly enantioselective direct aldol reaction catalyzed by organic molecules
-
Raj, M., Maya, V., Ginotra, S.K., and Singh, V.K. (2006) Highly enantioselective direct aldol reaction catalyzed by organic molecules. Org. Lett., 8, 4097-4099.
-
(2006)
Org. Lett.
, vol.8
, pp. 4097-4099
-
-
Raj, M.1
Maya, V.2
Ginotra, S.K.3
Singh, V.K.4
-
137
-
-
0037955602
-
Novel small organic molecules for a highly enantioselective direct aldol reaction
-
Tang, Z., Jiang, F., Yu, L.T., Cui, X., Gong, L.Z., Mi, A.Q., Jiang, Y.Z., and Wu, Y.D. (2003) Novel small organic molecules for a highly enantioselective direct aldol reaction. J. Am. Chem. Soc., 125, 5262-5263.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 5262-5263
-
-
Tang, Z.1
Jiang, F.2
Yu, L.T.3
Cui, X.4
Gong, L.Z.5
Mi, A.Q.6
Jiang, Y.Z.7
Wu, Y.D.8
-
138
-
-
1942469514
-
Enantioselective direct aldol reactions catalyzed by l-prolinamide derivatives
-
Tang, Z., Jiang, F., Cui, F., Gong, L.Z., Mi, A.Q., Jiang, Y.Z., and Wu, Y.D. (2004) Enantioselective direct aldol reactions catalyzed by l-prolinamide derivatives. Proc. Natl. Acad. Sci. U.S.A., 101, 5755-5760.
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 5755-5760
-
-
Tang, Z.1
Jiang, F.2
Cui, F.3
Gong, L.Z.4
Mi, A.Q.5
Jiang, Y.Z.6
Wu, Y.D.7
-
139
-
-
21244479264
-
A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes
-
Tang, Z., Yang, Z.H., Chen, X.H., Cun, L.F., Mi, A.Q., Jiang, Y.Z., and Gong, L.Z. (2005) A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes. J. Am. Chem. Soc., 127, 9285-9289.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9285-9289
-
-
Tang, Z.1
Yang, Z.H.2
Chen, X.H.3
Cun, L.F.4
Mi, A.Q.5
Jiang, Y.Z.6
Gong, L.Z.7
-
140
-
-
42649086790
-
Organo-catalyzed highly diastereoand enantio-selective direct aldol reactions in water
-
Zhao, J.-F., He, L., Jiang, J., Tang, Z., Cun, L.-F., and Gong, L.-Z. (2008) Organo-catalyzed highly diastereoand enantio-selective direct aldol reactions in water. Tetrahedron Lett., 49, 3372-3375.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3372-3375
-
-
Zhao, J.-F.1
He, L.2
Jiang, J.3
Tang, Z.4
Cun, L.-F.5
Gong, L.-Z.6
-
141
-
-
34547144181
-
Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium
-
Maya, V., Raj, M., and Singh, V.K. (2007) Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. Org. Lett., 9, 2593-2595.
-
(2007)
Org. Lett.
, vol.9
, pp. 2593-2595
-
-
Maya, V.1
Raj, M.2
Singh, V.K.3
-
142
-
-
33846318551
-
Organocatalyzed highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone and fluoroacetone in aqueous media: the use of water to control regioselectivity
-
Chen, X.H., Tang, Z., Luo, S.W., Cun, L.F., Mi, A.Q., Jiang, Y.Z., and Gong, L.Z. (2007) Organocatalyzed highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone and fluoroacetone in aqueous media: the use of water to control regioselectivity. Chem. Eur. J., 13, 689-701.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 689-701
-
-
Chen, X.H.1
Tang, Z.2
Luo, S.W.3
Cun, L.F.4
Mi, A.Q.5
Jiang, Y.Z.6
Gong, L.Z.7
-
143
-
-
49549107813
-
Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water
-
Zu, L., Xie, H., Li, H., Wang, J., and Wang, W. (2008) Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water. Org. Lett., 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
-
144
-
-
35348850061
-
Highly stereoselective direct aldol reactions catalyzed by (S)-NOBIN-l-prolinamide
-
Russo, A., Botta, G., and Lattanzi, A. (2007) Highly stereoselective direct aldol reactions catalyzed by (S)-NOBIN-l-prolinamide. Tetrahedron, 63, 11886-11892.
-
(2007)
Tetrahedron
, vol.63
, pp. 11886-11892
-
-
Russo, A.1
Botta, G.2
Lattanzi, A.3
-
145
-
-
34147103331
-
Enantioselective direct aldol reaction "on water" promoted by chiral organic catalysts
-
Guizzetti, S., Benaglia, M., Raimondi, L., and Celentano, G. (2007) Enantioselective direct aldol reaction "on water" promoted by chiral organic catalysts. Org. Lett., 9, 1247-1250.
-
(2007)
Org. Lett.
, vol.9
, pp. 1247-1250
-
-
Guizzetti, S.1
Benaglia, M.2
Raimondi, L.3
Celentano, G.4
-
146
-
-
34248585917
-
Rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water
-
Wang, C., Jiang, Y., Zhang, X.-X., Huang, Y., Li, B.-G., and Zhang, G.-L. (2007) Rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water. Tetrahedron Lett., 48, 4281-4285.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 4281-4285
-
-
Wang, C.1
Jiang, Y.2
Zhang, X.-X.3
Huang, Y.4
Li, B.-G.5
Zhang, G.-L.6
-
147
-
-
34347233023
-
Dipeptide-catalyzed direct asymmetric aldol reactions in the presence of water
-
Lei, M., Shi, L., Li, G., Chen, S., Fang, W., Ge, Z., Cheng, T., and Li, R. (2007) Dipeptide-catalyzed direct asymmetric aldol reactions in the presence of water. Tetrahedron, 63, 7892-7898.
-
(2007)
Tetrahedron
, vol.63
, pp. 7892-7898
-
-
Lei, M.1
Shi, L.2
Li, G.3
Chen, S.4
Fang, W.5
Ge, Z.6
Cheng, T.7
Li, R.8
-
148
-
-
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., and Wang, S. (2006) Highly efficient and reusable dendritic catalysts derived from N-prolylsulfonamide for the asymmetric direct aldol reaction in water. Org. Lett., 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
-
149
-
-
34548264706
-
Prolinamides derived from aminophenols as organocatalysts for asymmetric direct aldol reactions
-
Sathapornvajana, S. and Vilaivan, T. (2007) Prolinamides derived from aminophenols as organocatalysts for asymmetric direct aldol reactions. Tetrahedron, 63, 10253-10259.
-
(2007)
Tetrahedron
, vol.63
, pp. 10253-10259
-
-
Sathapornvajana, S.1
Vilaivan, T.2
-
150
-
-
33846615989
-
Direct asymmetric aldol reaction catalyzed by simple prolinamide phenols
-
Fu, Y.-Q., Li, Z.-C., Ding, L.-N., Tao, J.-C., Zhang, S.-H., and Tang, M.-S. (2006) Direct asymmetric aldol reaction catalyzed by simple prolinamide phenols. Tetrahedron: Asymmetry, 17, 3351-3357.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3351-3357
-
-
Fu, Y.-Q.1
Li, Z.-C.2
Ding, L.-N.3
Tao, J.-C.4
Zhang, S.-H.5
Tang, M.-S.6
-
151
-
-
34250700023
-
Organocatalytic asymmetric aldol reaction in the presence of water
-
Gryko, D. and Saletra, W.J. (2007) Organocatalytic asymmetric aldol reaction in the presence of water. Org. Biomol. Chem., 5, 2148-2153.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 2148-2153
-
-
Gryko, D.1
Saletra, W.J.2
-
152
-
-
34447128819
-
Polymer-supported proline-decorated dendrons: dendritic effect in asymmetric aldol reaction
-
Kehat, T. and Portnoy, M. (2007) Polymer-supported proline-decorated dendrons: dendritic effect in asymmetric aldol reaction. Chem. Commun., 2823-2825.
-
(2007)
Chem. Commun.
, pp. 2823-2825
-
-
Kehat, T.1
Portnoy, M.2
-
153
-
-
0346991371
-
Proline and benzylpenicillin derivatives grafted into mesoporous MCM-41: Novel organic- inorganic hybrid catalysts for direct aldol reaction
-
Dhar, D., Beadham, I., and Chandrasekaran, S. (2003) Proline and benzylpenicillin derivatives grafted into mesoporous MCM-41: Novel organic- inorganic hybrid catalysts for direct aldol reaction. Proc. Indian Acad. Sci., Chem. Sci., 115, 365-372.
-
(2003)
Proc. Indian Acad. Sci., Chem. Sci.
, vol.115
, pp. 365-372
-
-
Dhar, D.1
Beadham, I.2
Chandrasekaran, S.3
-
154
-
-
33846376783
-
Functionalized ionic liquids catalyzed direct aldol reactions
-
Luo, S., Mi, X., Zhang, L., Liu, S., Xu, H., and Cheng, J.-P. (2007) Functionalized ionic liquids catalyzed direct aldol reactions. Tetrahedron, 63, 1923-1930.
-
(2007)
Tetrahedron
, vol.63
, pp. 1923-1930
-
-
Luo, S.1
Mi, X.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.-P.6
-
155
-
-
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., Lo Meo, P., Riela, S., and Noto, R. (2008) New simple hydrophobic proline derivatives as highly active and stereoselective catalysts for the direct asymmetric aldol reaction in aqueous medium. Adv. Synth. Catal., 350, 2747-2760.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2747-2760
-
-
Giacalone, F.1
Gruttadauria, M.2
Lo Meo, P.3
Riela, S.4
Noto, R.5
-
156
-
-
58549088057
-
Stereoselective aldol reaction catalyzed by a highly recyclable polystyrene supported substituted prolinamide catalyst
-
Gruttadauria, M., Giacalone, F., Mossuto Marculescu, A., Salvo, A.M.P., and Noto, R. (2009) Stereoselective aldol reaction catalyzed by a highly recyclable polystyrene supported substituted prolinamide catalyst. ARKIVOC, (viii), 5-15.
-
(2009)
ARKIVOC
, Issue.8
, pp. 5-15
-
-
Gruttadauria, M.1
Giacalone, F.2
Mossuto Marculescu, A.3
Salvo, A.M.P.4
Noto, R.5
-
157
-
-
33748570123
-
Asymmetric direct aldol reaction catalysed by l-prolinethioamides
-
Gryko, D. and Lipiński, R. (2006) Asymmetric direct aldol reaction catalysed by l-prolinethioamides. Eur. J. Org. Chem., 3864-3876.
-
(2006)
Eur. J. Org. Chem.
, pp. 3864-3876
-
-
Gryko, D.1
Lipiński, R.2
-
158
-
-
0036021860
-
Synthesis and antibacterial activity of 1 β-methylcarbapenems having a 2,2-disubstituted-1,3-diazabicyclo[3.3.0] octan-4-one moiety and related compounds
-
Oh, C.-H., Dong, H.-G., Cho, H.-W., Park, S.J., Hong, J.H., Baek, D., and Cho, J.-H. (2002) Synthesis and antibacterial activity of 1 β-methylcarbapenems having a 2,2-disubstituted-1,3-diazabicyclo[3.3.0] octan-4-one moiety and related compounds. Part III. Arch. Pharm. Pharm. Med. Chem., 335, 200-206.
-
(2002)
Part III. Arch. Pharm. Pharm. Med. Chem.
, vol.335
, pp. 200-206
-
-
Oh, C.-H.1
Dong, H.-G.2
Cho, H.-W.3
Park, S.J.4
Hong, J.H.5
Baek, D.6
Cho, J.-H.7
-
159
-
-
0033054737
-
N-terminal 4-imidazolidinone prodrugs of Leu-enkephalin: synthesis, chemical and enzymatic stability studies
-
Bak, A., Fich, M., Larsen, B.D., Frokjaer, S., and Friis, G.J. (1999) N-terminal 4-imidazolidinone prodrugs of Leu-enkephalin: synthesis, chemical and enzymatic stability studies. Eur. J. Pharm. Sci., 7, 317-323.
-
(1999)
Eur. J. Pharm. Sci.
, vol.7
, pp. 317-323
-
-
Bak, A.1
Fich, M.2
Larsen, B.D.3
Frokjaer, S.4
Friis, G.J.5
-
160
-
-
18844460678
-
Design of an axially chiral amino acid with a binaphthyl backbone as an organocatalyst for a direct asymmetric aldol reaction
-
Kano, T., Takai, J., Tokuda, O., and Maruoka, K. (2005) Design of an axially chiral amino acid with a binaphthyl backbone as an organocatalyst for a direct asymmetric aldol reaction. Angew. Chem. Int. Ed., 44, 3055-3057.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 3055-3057
-
-
Kano, T.1
Takai, J.2
Tokuda, O.3
Maruoka, K.4
-
161
-
-
33645507049
-
Thermal effects in the organocatalytic asymmetric Mannich reaction
-
Rodríguez, B. and Bolm, C. (2006) Thermal effects in the organocatalytic asymmetric Mannich reaction. J. Org. Chem., 71, 2888-2891.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 2888-2891
-
-
Rodríguez, B.1
Bolm, C.2
-
162
-
-
38049151296
-
Highly diastereo- and enantioselective direct aldol reactions of aldehydes and ketones catalyzed by siloxyproline in the presence of water
-
Aratake, S., Itoh, T., Okano, T., Nagae, N., Sumiya, T., Shoji, M., and Hayashi, Y. (2007) Highly diastereo- and enantioselective direct aldol reactions of aldehydes and ketones catalyzed by siloxyproline in the presence of water. Chem. Eur. J., 13, 10246-10256.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 10246-10256
-
-
Aratake, S.1
Itoh, T.2
Okano, T.3
Nagae, N.4
Sumiya, T.5
Shoji, M.6
Hayashi, Y.7
-
163
-
-
28944449340
-
Acid-free, organocatalytic acetalization
-
Kotke, M. and Schreiner, P.R. (2006) Acid-free, organocatalytic acetalization. Tetrahedron, 62, 434-439.
-
(2006)
Tetrahedron
, vol.62
, pp. 434-439
-
-
Kotke, M.1
Schreiner, P.R.2
-
164
-
-
58549103519
-
The ion tag strategy as a route to highly efficient organocatalysts for the direct asymmetric aldol reaction
-
Lombardo, M., Easwar, S., Pasi, F., and Trombini, C. (2009) The ion tag strategy as a route to highly efficient organocatalysts for the direct asymmetric aldol reaction. Adv. Synth. Catal., 351, 276-282.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 276-282
-
-
Lombardo, M.1
Easwar, S.2
Pasi, F.3
Trombini, C.4
-
165
-
-
13444267885
-
Enantioselective organocatalyzed a sulfenylation of aldehydes
-
Marigo, M., Wabnitz, T.C., Fielenbach, D., and Jørgensen, K.A. (2005) Enantioselective organocatalyzed a sulfenylation of aldehydes. Angew. Chem. Int. Ed., 44, 794-797.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 794-797
-
-
Marigo, M.1
Wabnitz, T.C.2
Fielenbach, D.3
Jørgensen, K.A.4
-
166
-
-
34547178180
-
Asymmetric organocatalytic α-arylation of aldehydes
-
Alemán, J., Cabrera, S., Maerten, E., Overgaard, J., and Jørgensen, K.A. (2007) Asymmetric organocatalytic α-arylation of aldehydes. Angew. Chem. Int. Ed., 46, 5520-5523.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 5520-5523
-
-
Alemán, J.1
Cabrera, S.2
Maerten, E.3
Overgaard, J.4
Jørgensen, K.A.5
-
167
-
-
51749120761
-
Organocatalytic asymmetric synthesis of a,α-disubstituted α-amino acids and derivatives
-
Cabrera, S., Reyes, E., Alemán, J., Milelli, A., Kobbelgaard, S., and Jørgensen, K.A. (2008) Organocatalytic asymmetric synthesis of a,α-disubstituted α-amino acids and derivatives. J. Am. Chem. Soc., 130, 12031-12037.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12031-12037
-
-
Cabrera, S.1
Reyes, E.2
Alemán, J.3
Milelli, A.4
Kobbelgaard, S.5
Jørgensen, K.A.6
-
168
-
-
33845505476
-
Diarylprolinol ethers: expanding the potential of enamine/iminium-ion catalysis
-
Palomo, C. and Mielgo, A. (2006) Diarylprolinol ethers: expanding the potential of enamine/iminium-ion catalysis. Angew. Chem. Int. Ed., 45, 7876-7880.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7876-7880
-
-
Palomo, C.1
Mielgo, A.2
-
169
-
-
29844457732
-
A general organocatalyst for direct α-functionalization of aldehydes: stereoselective C-C, C-N, C-F, C-Br, and C-S bond-forming reactions
-
Franzén, J., Marigo, M., Fielenbach, D., Wabnitz, T.C., Kjærsgaard, A., and Jørgensen, K.A. (2005) A general organocatalyst for direct α-functionalization of aldehydes: stereoselective C-C, C-N, C-F, C-Br, and C-S bond-forming reactions. Scope and mechanistic insights. J. Am. Chem. Soc., 127, 18296-18304.
-
(2005)
Scope and mechanistic insights. J. Am. Chem. Soc.
, vol.127
, pp. 18296-18304
-
-
Franzén, J.1
Marigo, M.2
Fielenbach, D.3
Wabnitz, T.C.4
Kjærsgaard, A.5
Jørgensen, K.A.6
-
170
-
-
55449103171
-
One-pot catalytic enantioselective domino nitro-Michael/Michael synthesis of cyclopentanes with four stereocenters
-
Zhao, G.-L., Ibrahem, I., Dziedzic, P., Sun, J., Bonneau, C., and Córdova, A. (2008) One-pot catalytic enantioselective domino nitro-Michael/Michael synthesis of cyclopentanes with four stereocenters. Chem. Eur. J., 14, 10007-10011.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 10007-10011
-
-
Zhao, G.-L.1
Ibrahem, I.2
Dziedzic, P.3
Sun, J.4
Bonneau, C.5
Córdova, A.6
-
171
-
-
55549148449
-
Organocatalytic approach to benzofused nitrogen-containing heterocycles: enantioselective total synthesis of (+)-Angustureine
-
Fustero, S., Moscardó, J., Jiménez, D., Pérez-Carrión, M.D., Sánchez-Roselló, M., and del Pozo, C. (2008) Organocatalytic approach to benzofused nitrogen-containing heterocycles: enantioselective total synthesis of (+)-Angustureine. Chem. Eur. J., 14, 9868-9872.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 9868-9872
-
-
Fustero, S.1
Moscardó, J.2
Jiménez, D.3
Pérez-Carrión, M.D.4
Sánchez-Roselló, M.5
del Pozo, C.6
-
172
-
-
53549115929
-
A short route to α-Tocopherol
-
Liu, K., Chougnet, A., and Woggon, W.-D. (2008) A short route to α-Tocopherol. Angew. Chem. Int. Ed., 47, 5827-5829.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 5827-5829
-
-
Liu, K.1
Chougnet, A.2
Woggon, W.-D.3
-
173
-
-
33645354328
-
Chemistry of carbon nanotubes
-
Tasis, D., Tagmatarchis, N., Bianco, A., and Prato, M. (2006) Chemistry of carbon nanotubes. Chem. Rev., 106, 1105-1136.
-
(2006)
Chem. Rev.
, vol.106
, pp. 1105-1136
-
-
Tasis, D.1
Tagmatarchis, N.2
Bianco, A.3
Prato, M.4
-
174
-
-
0034830906
-
Modular chemistry: secondary building units as a basis for the design of highly porous and robust metal-organic carboxylate frameworks
-
Eddaoudi, M., Moler, D.B., Li, H., Chen, B., Reineke, T.M., O'Keeffe, M., and Yaghi, O.M. (2001) Modular chemistry: secondary building units as a basis for the design of highly porous and robust metal-organic carboxylate frameworks. Acc. Chem. Res., 34, 319-330.
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 319-330
-
-
Eddaoudi, M.1
Moler, D.B.2
Li, H.3
Chen, B.4
Reineke, T.M.5
O'Keeffe, M.6
Yaghi, O.M.7
-
175
-
-
0033581908
-
Design and synthesis of an exceptionally stable and highly porous metal- organic framework
-
Li, H., Eddaoudi, M., O'Keeffe, M., and Yaghi, O.M. (1999) Design and synthesis of an exceptionally stable and highly porous metal- organic framework. Nature, 402, 276-279.
-
(1999)
Nature
, vol.402
, pp. 276-279
-
-
Li, H.1
Eddaoudi, M.2
O'Keeffe, M.3
Yaghi, O.M.4
-
176
-
-
0142244286
-
Metal-organic frameworks
-
James, S.L. (2003) Metal-organic frameworks. Chem. Soc. Rev., 32, 276-288.
-
(2003)
Chem. Soc. Rev.
, vol.32
, pp. 276-288
-
-
James, S.L.1
-
177
-
-
52049087094
-
Catalytic properties of MIL-101
-
Henschel, A., Gedrich, K., Kraehnert, R., and Kaskel, S. (2008) Catalytic properties of MIL-101. Chem. Commun., 4192-4194.
-
(2008)
Chem. Commun.
, pp. 4192-4194
-
-
Henschel, A.1
Gedrich, K.2
Kraehnert, R.3
Kaskel, S.4
-
178
-
-
21244446924
-
A homochiral porous metal-organic framework for highly enantioselective heterogeneous asymmetric catalysis
-
Wu, C.-D., Hu, A., Zhang, L., and Lin, W. (2005) A homochiral porous metal-organic framework for highly enantioselective heterogeneous asymmetric catalysis. J.Am Chem. Soc., 127, 8940-8941.
-
(2005)
J.Am Chem. Soc.
, vol.127
, pp. 8940-8941
-
-
Wu, C.-D.1
Hu, A.2
Zhang, L.3
Lin, W.4
-
179
-
-
58149522303
-
Amino-based metal-organic frameworks as stable, highly active basic catalysts
-
Gascon, J., Aktay, U., Hernandez-Alonso, M.D., van Klink, G.P.M., and Kapteijn, F. (2009) Amino-based metal-organic frameworks as stable, highly active basic catalysts. J. Catal., 261, 75-87.
-
(2009)
J. Catal.
, vol.261
, pp. 75-87
-
-
Gascon, J.1
Aktay, U.2
Hernandez-Alonso, M.D.3
van Klink, G.P.M.4
Kapteijn, F.5
-
180
-
-
60849087034
-
Synthesis, structural characterization and selectively catalytic properties of metal- organic frameworks with nano-sized channels: a modular design strategy
-
doi: 10.1016/ j.jssc.2008.11.018
-
Qiu, L.-G., Gu, L.-N., Hu, G., and Zhang, L.-D. (2009) Synthesis, structural characterization and selectively catalytic properties of metal- organic frameworks with nano-sized channels: a modular design strategy. J. Sol. State Chem. doi: 10.1016/ j.jssc.2008.11.018.
-
(2009)
J. Sol. State Chem
-
-
Qiu, L.-G.1
Gu, L.-N.2
Hu, G.3
Zhang, L.-D.4
|