Literature DB >> 19368378

Aldol-type chirons from asymmetric hydrogenations of trisubstituted alkenes.

Jian Zhao1, Kevin Burgess.   

Abstract

Catalyst control dominates in the asymmetric hydrogenations of largely unfunctionalized trisubstituted alkenes formed from lactic acid and glyceraldehyde, affording syn- and anti-aldol products of the type shown above.

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Year:  2009        PMID： 19368378     DOI： 10.1021/ol900308w

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


  3 in total

1.  A comparison between oxazoline-imidazolinylidene, -imidazolylidine, -benzimidazolylidene hydrogenation catalysts.

Authors:  Sakunchai Khumsubdee; Yubo Fan; Kevin Burgess
Journal:  J Org Chem       Date:  2013-09-19       Impact factor: 4.354

2.  Homo-Roche ester derivatives by asymmetric hydrogenation and organocatalysis.

Authors:  Sakunchai Khumsubdee; Hua Zhou; Kevin Burgess
Journal:  J Org Chem       Date:  2013-11-12       Impact factor: 4.354

3.  Comparison Of Asymmetric Hydrogenations Of Unsaturated- Carboxylic Acids And -Esters.

Authors:  Sakunchai Khumsubdee; Kevin Burgess
Journal:  ACS Catal       Date:  2013-02-01       Impact factor: 13.084
  3 in total

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