Literature DB >> 12126434

InBr3-catalyzed Friedel-Crafts addition of indoles to chiral aromatic epoxides: a facile route to enantiopure indolyl derivatives.

Marco Bandini1, Pier Giorgio Cozzi, Paolo Melchiorre, Achille Umani-Ronchi.   

Abstract

Aromatic optically active epoxides can be opened in a regioselective and clean way with indoles in the presence of catalytic amount of InBr3 (1 mol %). The reaction takes place with a SN2 pathway affording the 2-aryl-2-(3'-indolyl)ethan-1-ols with excellent enantioselectivity (ee up to 99%).

Entities:  

Year:  2002        PMID: 12126434     DOI: 10.1021/jo0256235

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Remarkably mild and efficient intramolecular Friedel-Crafts cyclization catalyzed by In(III).

Authors:  Ryuji Hayashi; Gregory R Cook
Journal:  Org Lett       Date:  2007-03-09       Impact factor: 6.005

  1 in total

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