Highly Enantioselective Benzoin Condensation Reactions Involving a Bifunctional Protic Pentafluorophenyl-Substituted Triazolium Precatalyst

Baragwanath, Louise and Rose, Christopher A. and Zeitler, Kirsten and Connon, Stephen J. (2009) Highly Enantioselective Benzoin Condensation Reactions Involving a Bifunctional Protic Pentafluorophenyl-Substituted Triazolium Precatalyst. JOURNAL OF ORGANIC CHEMISTRY, 74 (23). pp. 9214-9217. ISSN 0022-3263,

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Abstract

Improved catalyst design by incorporating a hydrogen bond donating substituent to improve enantiocontrol together with an acidifying pentafluorophenyl substituent to enhance catalyst efficiency results in a triazolium ion precatalyst that promotes the asymmetric archetypal benzoin condensation with excellent efficiency and unprecedented enantioselectivity.

Item Type: Article
Uncontrolled Keywords: N-HETEROCYCLIC CARBENES; ASYMMETRIC STETTER REACTION; BICYCLIC THIAZOLIUM SALTS; CHIRAL THIAZOLIUM; CATALYSIS; INDUCTION; KETENES;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Alumni or Retired Professors > Arbeitskreis Dr. Kirsten Zeitler
Depositing User: Dr. Gernot Deinzer
Date Deposited: 27 Aug 2020 10:27
Last Modified: 27 Aug 2020 10:27
URI: https://pred.uni-regensburg.de/id/eprint/27992

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