-
1
-
-
0000238602
-
Reversing selectivity of cyclodextrin bisimidazole ribonuclease limics by changing the catalyst geometry
-
(a) Breslow, R.; Bovy, P.; Hersh, C. L. Reversing selectivity of cyclodextrin bisimidazole ribonuclease limics by changing the catalyst geometry. J. Am. Chem. Sac. 1980, 102, 2115-2117;
-
(1980)
J. Am. Chem. Sac.
, vol.102
, pp. 2115-2117
-
-
Breslow, R.1
Bovy, P.2
Hersh, C.L.3
-
2
-
-
0001300546
-
Selective Diels-Alder reactions in aqueous solutions and suspensions
-
(b) Breslow, R.; Maitra, U.; Rideout, D. Selective Diels-Alder reactions in aqueous solutions and suspensions. Tetrahedron Lett. 1983, 24, 1901-1904.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 1901-1904
-
-
Breslow, R.1
Maitra, U.2
Rideout, D.3
-
3
-
-
0001667614
-
Water as a solvent for the Claisen rearranggement: Practical kinetic implications for synthetic organic chemistry
-
(a) Grieco, P. A.; Brandes, E. B.; McCann, S.; Clark, J. D. Water as a solvent for the Claisen rearranggement: Practical kinetic implications for synthetic organic chemistry. J. Org. Chem. 1989, 54, 5849-5851;
-
(1989)
J. Org. Chem.
, vol.54
, pp. 5849-5851
-
-
Grieco, P.A.1
Brandes, E.B.2
McCann, S.3
Clark, J.D.4
-
4
-
-
0011520443
-
Secondary deuterium kinetic isotope effects in the aqueaus Claisen rearrangement: Evidence against an ionic transition state
-
(b) Gajewski, J. J.; Brichford, N. L. Secondary deuterium kinetic isotope effects in the aqueaus Claisen rearrangement: Evidence against an ionic transition state. J. Am. Chem. Soc. 1994, 116, 3165.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 3165
-
-
Gajewski, J.J.1
Brichford, N.L.2
-
5
-
-
0033532244
-
Remarkable enhancement of reactivity by Brønsted acids in aldol reactions mediated by Lewis acid-surfactant-combined catalysts in water
-
(a) Manabe, K.; Kobayashi, S. Remarkable enhancement of reactivity by Brønsted acids in aldol reactions mediated by Lewis acid-surfactant- combined catalysts in water. Tetrahedron Lett. 1999, 40, 3773-3776;
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3773-3776
-
-
Manabe, K.1
Kobayashi, S.2
-
6
-
-
0033575446
-
Catalytic asymmetric Mukaiyama aldol reactions in aqueous media
-
(b) Kobayashi, S.; Nagayama, S.; Busujima, T. Catalytic asymmetric Mukaiyama aldol reactions in aqueous media. Tetrahedron 1999, 55, 8739-8746.
-
(1999)
Tetrahedron
, vol.55
, pp. 8739-8746
-
-
Kobayashi, S.1
Nagayama, S.2
Busujima, T.3
-
7
-
-
0031763196
-
Effects of the hydrophobicity of the reactants on Diels-Alder reactions in water
-
(a) Meijer, A.; Otto, S.; Jan, B. F. N. E. Effects of the hydrophobicity of the reactants on Diels-Alder reactions in water. J. Org. Chem. 1998, 63, 8989-8994;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8989-8994
-
-
Meijer, A.1
Otto, S.2
Jan, B.F.N.E.3
-
8
-
-
0001648506
-
A chiral Lewis-acid catalyzed Diels-Alder reaction. Water-enhanced enantioselectivity
-
(b) Otto, S.; Boccaletti, G.; Jan, B. F. N. E. A chiral Lewis-acid catalyzed Diels-Alder reaction. Water-enhanced enantioselectivity. J. Am. Chem. Soc. 1998, 120, 4238-4239.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 4238-4239
-
-
Otto, S.1
Boccaletti, G.2
Jan, B.F.N.E.3
-
9
-
-
0029932703
-
Ytterbium inflate catalyzed Michael additions of β-ketoesters in water
-
(a) Keller, E.; Feringa, B. L. Ytterbium inflate catalyzed Michael additions of β-ketoesters in water. Tetrahedron Lett. 1996, 37, 1879-1882;
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 1879-1882
-
-
Keller, E.1
Feringa, B.L.2
-
10
-
-
0034701460
-
Michael reactions in water using Lewis acid-surfactant-combined catalysts
-
(b) Mori, Y.; Kakumoto, K.; Manabe, K.; Kobayashi, S. Michael reactions in water using Lewis acid-surfactant-combined catalysts. Tetrahedron Lett. 2000, 41, 3107-3111.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 3107-3111
-
-
Mori, Y.1
Kakumoto, K.2
Manabe, K.3
Kobayashi, S.4
-
13
-
-
0000677232
-
Organic reactions in aqueous media - With a focus on carbon-carbon bond formation
-
(c) Li, C. J. Organic reactions in aqueous media - with a focus on carbon-carbon bond formation. Chem. Rev. 1993, 93, 2023-2035.
-
(1993)
Chem. Rev.
, vol.93
, pp. 2023-2035
-
-
Li, C.J.1
-
14
-
-
0035974365
-
Clean synthesis in water. Part 2: Uncatalysed condensation reaction of Meldrum's acid and aldehydes
-
Bigi, F.; Carloni, S.; Ferrari, L.; Maggi, R.; Mazzacani, A.; Sartori, G. Clean synthesis in water. Part 2: Uncatalysed condensation reaction of Meldrum's acid and aldehydes. Tetrahedron Lett. 2001, 42, 5203-5205.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 5203-5205
-
-
Bigi, F.1
Carloni, S.2
Ferrari, L.3
Maggi, R.4
Mazzacani, A.5
Sartori, G.6
-
15
-
-
0033543484
-
Effects of Lewis acid-surfactant-combined catalysts on aldol and Diels-Alder reactions in water
-
(a) Manabe, K.; Mori, Y.; Kobayashi, S. Effects of Lewis acid-surfactant-combined catalysts on aldol and Diels-Alder reactions in water. Tetrahedron 1999, 55, 11203-11208;
-
(1999)
Tetrahedron
, vol.55
, pp. 11203-11208
-
-
Manabe, K.1
Mori, Y.2
Kobayashi, S.3
-
16
-
-
0034701460
-
Michael reactions in water using Lewis acid-surfactant-combined catalysts
-
(b) Mori, Y.; Kakumoto, K.; Manabe, K.; Kobayashi, S. Michael reactions in water using Lewis acid-surfactant-combined catalysts. Tetrahedron Lett. 2000, 41, 3107-3111;
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 3107-3111
-
-
Mori, Y.1
Kakumoto, K.2
Manabe, K.3
Kobayashi, S.4
-
17
-
-
0032560708
-
Scandium trisdodecylsulfate (STDS): A new type of Lewis acid that forms stable dispersion systems with organic substrates in water and accelerates aldol reactions much faster in water than in organic solvents
-
(c) Kobayashi, S.; Wakabayashi, T. Scandium trisdodecylsulfate (STDS): A new type of Lewis acid that forms stable dispersion systems with organic substrates in water and accelerates aldol reactions much faster in water than in organic solvents. Tetrahedron Lett. 1998, 39, 5389-5392;
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5389-5392
-
-
Kobayashi, S.1
Wakabayashi, T.2
-
18
-
-
0033532244
-
Remarkable enhancement of reactivity by Brønsted acids in aldol reactions mediated by Lewis acid-surfactant-combined catalysts in water
-
(d) Manabe, K.; Kobaashi, S. Remarkable enhancement of reactivity by Brønsted acids in aldol reactions mediated by Lewis acid-surfactant- combined catalysts in water. Tetrahedron Lett. 1999, 40, 3773-3776.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 3773-3776
-
-
Manabe, K.1
Kobaashi, S.2
-
19
-
-
0346340416
-
Catalysis of organic reactions by inorganic solids
-
(a) Laszlo, P. Catalysis of organic reactions by inorganic solids. Acc. Chem. Res. 1986, 19, 121-127;
-
(1986)
Acc. Chem. Res.
, vol.19
, pp. 121-127
-
-
Laszlo, P.1
-
20
-
-
0033525186
-
Montmorillonite KSF as an inorganic, water stable, and reusable catalyst for the Knoevenagel synthesis of coumarin-3-carboxylic acids
-
(b) Bigi, F.; Chesini, L.; Maggi, R.; Sartori, G. Montmorillonite KSF as an inorganic, water stable, and reusable catalyst for the Knoevenagel synthesis of coumarin-3-carboxylic acids. J. Org. Chem. 1999, 64, 1033-1035;
-
(1999)
J. Org. Chem.
, vol.64
, pp. 1033-1035
-
-
Bigi, F.1
Chesini, L.2
Maggi, R.3
Sartori, G.4
-
21
-
-
37049070934
-
The use of a high surface area silicon oxynitride as a solid basic catalyst
-
(c) Lednor, P. W.; de Ruiter, R. The use of a high surface area silicon oxynitride as a solid basic catalyst. J. Chem. Soc., Chem. Commun. 1991, 1625-1626.
-
(1991)
J. Chem. Soc., Chem. Commun.
, pp. 1625-1626
-
-
Lednor, P.W.1
De Ruiter, R.2
-
22
-
-
0007326878
-
The solid-state Michael addition of 3-methyl-1-phenyl-5-pyrazolone
-
(a) Li, X.-L.; Wang, Y.-M.; Tian, B.; Teruo, M.; Meng, J.-B. The solid-state Michael addition of 3-methyl-1-phenyl-5-pyrazolone. J. Heterocycl. Chem. 1998, 35, 129-134;
-
(1998)
J. Heterocycl. Chem.
, vol.35
, pp. 129-134
-
-
Li, X.-L.1
Wang, Y.-M.2
Tian, B.3
Teruo, M.4
Meng, J.-B.5
-
23
-
-
3042836116
-
Uncatalyzed microwave-enhanced reaction of 1-phenyl-3-methylpyrazol-5-one with aromatic aldehydes under solvent-free conditions
-
(b) Bai, Y.-J.; Li, M.; Lu, J. Wang, Z.-J. Uncatalyzed microwave-enhanced reaction of 1-phenyl-3-methylpyrazol-5-one with aromatic aldehydes under solvent-free conditions. Chinese J. Org. Chem. 2004, 24, 616-620.
-
(2004)
Chinese J. Org. Chem.
, vol.24
, pp. 616-620
-
-
Bai, Y.-J.1
Li, M.2
Lu, J.3
Wang, Z.-J.4
|