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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 18, 1988 - Issue 13
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Original Articles

Asymmetric Reduction of Prochiral Ketones in Aqueous Micelles of Chiral Surfactants (-)-Trialkylmskthylammcnium Bromides

Yongmin Zhang Department of Chemistry, Hangzhou University, Hangzhou, P. R. of China
,
Weiqiang Far Department of Chemistry, Hangzhou University, Hangzhou, P. R. of China
,
Ping Lu Department of Chemistry, Hangzhou University, Hangzhou, P. R. of China
&
Wei Wang Department of Chemistry, Hangzhou University, Hangzhou, P. R. of China
Pages 1495-1500 | Published online: 03 Jan 2007

Citations (16)

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Read on this site (2)

Y.K. Yarovoy & M.M. Labes. (1997) Influence of Cholesteric Solvents on the Kinetics of Schiff Base Formation from Enantiomeric Amines. Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 292:1, pages 163-174.
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Yongimin Zhang, Weiliang Boa & Hong Dong. (1993) The Asymmetric Solvomercuration-Demercuation of Olefins in Chiral Micellar Systems. Synthetic Communications 23:21, pages 3029-3035.
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Articles from other publishers (14)

Sangita Roy, Debapratim Das, Antara Dasgupta, Rajendra Narayan Mitra & Prasanta Kumar Das. (2005) Amino Acid Based Cationic Surfactants in Aqueous Solution:  Physicochemical Study and Application of Supramolecular Chirality in Ketone Reduction. Langmuir 21:23, pages 10398-10404.
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N. Mariano Correa, Daniel H. Zorzan, Marco Chiarini & Giorgio Cerichelli. (2004) Reverse Micellar Aggregates:  Effect on Ketone Reduction. 1. Substrate Role. The Journal of Organic Chemistry 69:24, pages 8224-8230.
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N. Mariano Correa, Daniel H. Zorzan, Loredana D'Anteo, Ermanno Lasta, Marco Chiarini & Giorgio Cerichelli. (2004) Reverse Micellar Aggregates:  Effect on Ketone Reduction. 2. Surfactant Role. The Journal of Organic Chemistry 69:24, pages 8231-8238.
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Tammy A Davidson, Kalyan Mondal & Xiaoye Yang. (2004) Use of a chiral surfactant for enantioselective reduction of a ketone. Journal of Colloid and Interface Science 276:2, pages 498-502.
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Michael John Diego-Castro, Helen Claire Hailes & Margaret Jayne Lawrence. (2001) Synthesis and Characterization of Optically Active Surfactants Derived from Phenylalanine and Leucine. Journal of Colloid and Interface Science 234:1, pages 122-126.
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Weidu Wu & Yongmin Zhang. (1998) Enantioselective synthesis of α-amino acids in chiral reverse micelles. Tetrahedron: Asymmetry 9:8, pages 1441-1444.
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Yongmin Zhang & Weidu Wu. (1997) Enantioselective synthesis of β-hydroxy esters by Reformatsky reactions in chiral micelles. Tetrahedron: Asymmetry 8:21, pages 3575-3578.
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Yongmin Zhang & Weidu Wu. (1997) Enantioselective synthesis of oxiranes by the reactions of dimethylsulfonium methylide and aromatic aldehydes and ketones in the presence of chiral micelles. Tetrahedron: Asymmetry 8:16, pages 2723-2725.
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Yongmin Zhang & Peipei Sun. (1996) The asymmetric induction and catalysis of chiral reverse micelle: Asymmetric reduction of prochiral ketones. Tetrahedron: Asymmetry 7:11, pages 3055-3058.
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Elodie Liotier, Guy Mousset & Christine Mousty. (1995) Electrochemical and spectroscopic behavior of trifluoromethylacetophenone in aqueous and micellar medium. Canadian Journal of Chemistry 73:9, pages 1488-1496.
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V. I. Zlobina, N. M. Libman & S. M. Ramsh. (1993) Chemical reduction of arylketones to optically active alcohols (review). Pharmaceutical Chemistry Journal 27:8, pages 596-605.
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Chantal Larpent & Xavier Chasseray. (1992) Optically active surfactants - I - the first synthesis and properties of sodium bis [(S)] ethyl-2-hexyl] sulfosuccinates (“aerosal ot”). Tetrahedron 48:19, pages 3903-3914.
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Yong‐Min Zhang, Chun‐Ling Fu & Wei‐Qiang Fan. (2011) Organic reactions in chiral micelles: 7. The structural effects on the asymmetric oxidation of prochiral sulfides in chiral micelles. Chinese Journal of Chemistry 8:1, pages 89-96.
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Y. ZHANG, W. FAN, P. LU & W. WANG. (2016) ChemInform Abstract: Asymmetric Reduction of Prochiral Ketones in Aqueous Micelles of Chiral Surfactants (‐)‐Trialkylmenthylammonium Bromides.. ChemInform 20:13.
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