Highly Enantioselective Reactions of Configurationally Labile α-Thioorganolithiums Using Chiral Bis(oxazoline)s via Two Different Enantiodetermining Steps-Reference-Cited by-同舟云学术

Highly Enantioselective Reactions of Configurationally Labile α-Thioorganolithiums Using Chiral Bis(oxazoline)s via Two Different Enantiodetermining Steps

Published:2000-11-05 Issue:46 Volume:122 Page:11340-11347
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nakamura Shuichi¹,Nakagawa Ryo¹,Watanabe Yoshihiko¹,Toru Takeshi¹

Affiliation:

1. Contribution from the Department of Applied Chemistry, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0025191

Reference101 articles.

1. Chiral Lithium-1-oxyalkanides by Asymmetric Deprotonation; Enantioselective Synthesis of 2-Hydroxyalkanoic Acids and Secondary Alkanols

2. Enantioselective Synthesis with Lithium/(−)-Sparteine Carbanion Pairs

3. Synthesis of the C10-C25 Northern Moiety of 22,23-Dihydroavermectin B1b

4. Convenient Synthesis of Enantiomerically Enriched β-Cyclopropylalaninol Derivatives by Kinetic Resolution via (-)-Sparteine-Mediated Deprotonation

5. Synthesis of Enantiomerically and Diastereomerically Pure Cyclopentanols by asymmetric Cyclocarbolithiation of 5-Alkenyl Carbamates

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