Literature DB >> 19743483

Bile acids in asymmetric synthesis and chiral discrimination.

Olga Bortolini1, Giancarlo Fantin, Marco Fogagnolo.   

Abstract

An overview on the use of bile acid-based compounds able to catalyze transformations, control the stereochemical course of a given reaction, recognize and bind other molecules, is presented. The recent developments in inclusion discrimination of chiral and achiral guests and enantioselective recognition achieved by bile acid are described with suitable examples. Copyright 2009 Wiley-Liss, Inc.

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Year:  2010        PMID: 19743483     DOI: 10.1002/chir.20769

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  2 in total

1.  Bis[3α,7α,12α-tris-(4-nitro-benzo-yloxy)-5β-cholan-24-yl] disulfide-ethyl acetate-n-hexane (4/4/1).

Authors:  Krzysztof Brzezinski; Aneta M Tomkiel; Zenon Lotowski; Jacek Morzycki; Zbigniew Dauter
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-12-11

2.  Oxidation of Sodium Deoxycholate Catalyzed by Gold Nanoparticles and Chiral Recognition Performances of Bile Salt Micelles.

Authors:  Jing Wang; Xu Xu; Hao Chen; Shuai-Shuai Zhang; Yin-Xian Peng
Journal:  Molecules       Date:  2019-12-09       Impact factor: 4.411

  2 in total

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