Highly Enantioselective Reaction of α-Selenoorganolithium Compounds with Chiral Bis(oxazoline)s and Preparation of Enantioenriched Benzylidencyclohexanes-Reference-Cited by-同舟云学术

Highly Enantioselective Reaction of α-Selenoorganolithium Compounds with Chiral Bis(oxazoline)s and Preparation of Enantioenriched Benzylidencyclohexanes

Published:2004-11-10 Issue:25 Volume:69 Page:8916-8923
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nakamura Shuichi¹,Aoki Takayuki¹,Ogura Takahiro¹,Wang Libo¹,Toru Takeshi¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo048505l

Reference73 articles.

1. Generation of a Configurationally Stable Chiral Benzyllithium Derivative, and the Capricious Stereochemistry of Its Electrophilic Substitution

2. Total Synthesis of 22,23-Dihydroavermectin B1bAglycone

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

4. (−)-Sparteine-mediated stereoselective intramolecular carbolithiation of alkynes

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