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

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

Published:2022-07-25 Issue:15 Volume:87 Page:10509-10515
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Miyazaki Kanako¹,Nakata Kenya¹^ORCID

Affiliation:

1. Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu Matsue, Shimane 690-8504, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01129

Reference55 articles.

1. Efficiency in Nonenzymatic Kinetic Resolution

2. Catalytic Non-Enzymatic Kinetic Resolution

3. Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols

4. Enantioselective Acylations Catalyzed by Chiral Phosphines

5. 2-Aryl-4,4,8-trimethyl-2-phosphabicyclo[3.3.0]octanes: Reactive Chiral Phosphine Catalysts for Enantioselective Acylation

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