Your browser doesn't support javascript.
loading
Stereoselective synthesis of 1,2-aminoalcohols by [2,3]-wittig rearrangements.
Barbazanges, Marion; Meyer, Christophe; Cossy, Janine.
Affiliation
  • Barbazanges M; Laboratoire de Chimie Organique, ESPCI, CNRS, 10 rue Vauquelin 75231 Paris Cedex 05, France.
Org Lett ; 9(17): 3245-8, 2007 Aug 16.
Article in En | MEDLINE | ID: mdl-17655314
ABSTRACT
[2,3]-Wittig rearrangements of (E)-3-aza-allylic alcohol derivatives can provide access to functionalized 1,2-aminoalcohols with high syn or anti diastereoselectivity depending on the anionic stabilizing group (amide or alkyne).
Subject(s)
Search on Google
Print
XML
PubMed Links

Database: MEDLINE Main subject: Amino Alcohols Language: En Year: 2007 Type: Article
Search on Google
Print
XML
PubMed Links

Database: MEDLINE Main subject: Amino Alcohols Language: En Year: 2007 Type: Article