Literature DB >> 19764789

Highly enantioselective Friedel-Crafts reaction of thiophenes with glyoxylates: formal synthesis of duloxetine.

Jakub Majer1, Piotr Kwiatkowski, Janusz Jurczak.   

Abstract

An efficient Friedel-Crafts reaction of a series of 2-substituted thiophenes with alkyl glyoxylates has been developed using a catalytic amount of an easy accessible 6,6'-dibromo-BINOL/Ti(IV) complex. A variety of hydroxy(thiophene-2-yl)acetates can be synthesized in high enantioselectivites (92-98% ee) and good yields. This is the first report on the efficient asymmetric F-C reaction of thiophenes with alkyl glyoxylates. Starting from simple thiophene and n-butyl glyoxylate, we demonstrated the formal synthesis of duloxetine.

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Year:  2009        PMID: 19764789     DOI: 10.1021/ol901906r

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Enzymatic enantioselective decarboxylative protonation of heteroaryl malonates.

Authors:  Ross Lewin; Mark Goodall; Mark L Thompson; James Leigh; Michael Breuer; Kai Baldenius; Jason Micklefield
Journal:  Chemistry       Date:  2015-03-12       Impact factor: 5.236

  1 in total

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