Literature DB >> 15200306

Synthesis of omega-hydroxy ketones from omega-benzyloxy Weinreb amides by using a chemoselective nucleophilic addition/Birch reduction process.

Catherine Taillier1, Véronique Bellosta, Christophe Meyer, Janine Cossy.   

Abstract

[reaction: see text] A chemoselective nucleophilic addition/Birch reduction process applied to omega-benzyloxy Weinreb amides led to omega-hydroxy ketones in good yields.

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Year:  2004        PMID： 15200306     DOI： 10.1021/ol049434f

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


  2 in total

1.  Effect of Substituents and Stability of Transient Aluminum-Aminals in the Presence of Nucleophiles.

Authors:  Francis J Barrios; Brannon C Springer; Robert A Hazlitt; David A Colby
Journal:  Synthesis (Stuttg)       Date:  2014-12-05       Impact factor: 3.157

2.  Simple, chemoselective hydrogenation with thermodynamic stereocontrol.

Authors:  Kotaro Iwasaki; Kanny K Wan; Alberto Oppedisano; Steven W M Crossley; Ryan A Shenvi
Journal:  J Am Chem Soc       Date:  2014-01-15       Impact factor: 15.419
  2 in total

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