Two-Step Kinetic Resolution of Racemic Secondary Benzylic Alcohols Using the Combination of Enantioselective Silylation and Acylation: One-Pot Procedure Catalyzed by Chiral Guanidine

A novel two-step kinetic resolution of racemic secondary benzylic alcohols with practical enantiomeric ratios was achieved. The reactions were carried out via a one-pot operation by combining enantioselective silylation and acylation mediated by the same chiral guanidine catalyst.

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Veröffentlicht in:Journal of organic chemistry 2022-08, Vol.87 (15), p.10509-10515
Hauptverfasser: Miyazaki, Kanako, Nakata, Kenya
Format: Artikel
Sprache:eng
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Zusammenfassung:A novel two-step kinetic resolution of racemic secondary benzylic alcohols with practical enantiomeric ratios was achieved. The reactions were carried out via a one-pot operation by combining enantioselective silylation and acylation mediated by the same chiral guanidine catalyst.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.2c01129