Literature DB >> 19055327

Complete switch of product selectivity in asymmetric direct aldol reaction with two different chiral organocatalysts from a common chiral source.

Keiji Nakayama1, Keiji Maruoka.   

Abstract

A novel approach for asymmetric synthesis of both enantiomeric aldol products has been developed by designing two different chiral organocatalysts from a readily available, protected cis-diamine compound as a common chiral source. This approach would be very useful from a practical viewpoint.

Entities:  

Year:  2008        PMID: 19055327     DOI: 10.1021/ja807807p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

Review 1.  The direct catalytic asymmetric aldol reaction.

Authors:  Barry M Trost; Cheyenne S Brindle
Journal:  Chem Soc Rev       Date:  2010-02-17       Impact factor: 54.564

2.  Metal-catalysed 1,2-diamination reactions.

Authors:  Francesca Cardona; Andrea Goti
Journal:  Nat Chem       Date:  2009-06-22       Impact factor: 24.427

3.  Bifunctional organic polymeric catalysts with a tunable acid-base distance and framework flexibility.

Authors:  Huanhui Chen; Yanan Wang; Qunlong Wang; Junhui Li; Shiqi Yang; Zhirong Zhu
Journal:  Sci Rep       Date:  2014-09-30       Impact factor: 4.379

4.  Enantiodivergence by minimal modification of an acyclic chiral secondary aminocatalyst.

Authors:  Jun Dai; Zhuang Wang; Yuhua Deng; Lei Zhu; Fangzhi Peng; Yu Lan; Zhihui Shao
Journal:  Nat Commun       Date:  2019-11-15       Impact factor: 14.919

  4 in total

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