Literature DB >> 23826677

Manipulating the diastereoselectivity of ortholithiation in planar chiral ferrocenes.

Simon A Herbert1, Dominic C Castell, Jonathan Clayden, Gareth E Arnott.   

Abstract

The sense of asymmetric ortholithiation directed by a chiral oxazoline may be inverted simply by the choice of achiral ligand. Comparison of results with a number of ferrocenyl oxazoline derivatives suggests that lithiation takes place by coordination to the oxazoline nitrogen irrespective of the ligand used.

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Year:  2013        PMID: 23826677     DOI: 10.1021/ol4013734

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


  1 in total

1.  Inherently chiral calix[4]arenes via oxazoline directed ortholithiation: synthesis and probe of chiral space.

Authors:  Simon A Herbert; Laura J van Laeren; Dominic C Castell; Gareth E Arnott
Journal:  Beilstein J Org Chem       Date:  2014-11-25       Impact factor: 2.883

  1 in total

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