Literature DB >> 20825148

Base-catalyzed isomerization of 2-isoxazolines enables a two-step enantioselective synthesis of β-hydroxynitriles from enals.

Antti Pohjakallio1, Petri M Pihko, Jun Liu.   

Abstract

The asymmetric synthesis of β-hydroxynitriles remains a challenge in organic synthesis. Herein we report a convenient synthesis of β-hydroxynitriles from enantiomerically enriched 3-unsubstituted 2-isoxazolines via a base-catalyzed ring-opening reaction that takes place without loss of enantiopurity. In combination with organocatalytic enantioselective synthesis of 3-unsubstituted 2-isoxazolines, the ring-opening enables a short 2-step synthesis of β-hydroxynitriles from α,β-unsaturated aldehydes in high enantiomeric purity.

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Year:  2010        PMID: 20825148     DOI: 10.1021/jo1013788

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


  1 in total

1.  N-O Cleavage reactions of heterobicycloalkene-fused 2-isoxazolines.

Authors:  Jaipal R Nagireddy; Geoffrey K Tranmer; Emily Carlson; William Tam
Journal:  Beilstein J Org Chem       Date:  2014-09-16       Impact factor: 2.883

  1 in total

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