Asymmetric [2,3]Wittig sigmatropic rearrangement involving a chiral azaenolate as the migrating terminus. A simple synthesis of (+)-verrucarinolactone-Reference-Cited by-同舟云学术

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Asymmetric [2,3]Wittig sigmatropic rearrangement involving a chiral azaenolate as the migrating terminus. A simple synthesis of (+)-verrucarinolactone

Published:1984-01 Issue:52 Volume:25 Page:6011-6014
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mikami Kōchi,Fujimoto Katsuhiko,Kasuga Takashi,Nakai Takeshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Acyclic stereocontrol via asymmetric [2,3]-Wittig rearrangement with high enantio- and erythro-selectivity and its use in the chiral synthesis of insect pheromones

2. HIGHLY ENANTIOSPECIFIC AND ERYTHRO-SELECTIVE [2,3]-WITTIG REARRANGEMENT OF ENANTIOMERICALLY-ENRICHED ALLYLIC BENZYL ETHERS. A NEW, FORMAL CHIRAL SYNTHESIS OFl-EPHEDRINE

Cited by 54 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Multi-gram-scale synthesis of a versatile syn-anti stereotriad by a short and cost-effective route;Arkivoc;2019-04-24

2. Asymmetric [2,3]-Wittig Rearrangement: Synthesis of Homoallylic, Allenylic, and Enynyl α-Benzyl Alcohols;Organic Letters;2018-12-10

3. Formation of Alcohols and Phenols by Ether Cleavage;Comprehensive Organic Transformations;2018-02-28

4. Development of a Phase-Transfer-Catalyzed, [2,3]-Wittig Rearrangement;The Journal of Organic Chemistry;2015-10-02

5. [2,3]-Wittig Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15

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