The stereochemistry of the Grignard — Ortho ester reaction revisited: Regioselective endocyclic cleavage in the reaction of Grignard reagents with cis-2-methoxy-4-methyl-1,3-dioxane-Reference-Cited by-同舟云学术

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The stereochemistry of the Grignard — Ortho ester reaction revisited: Regioselective endocyclic cleavage in the reaction of Grignard reagents with cis-2-methoxy-4-methyl-1,3-dioxane

Published:1997-06 Issue:23 Volume:38 Page:4047-4050
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bailey William F.,Croteau Allan A.,Rivera Alberto D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Carboxylic Ortho Acid Derivatives;DeWolfe,1970

2. Grignard Reactions of Nonmetallic Substances;Kharasch,1954

3. Chemistry of the Aliphatic Orthoesters;Post,1943

4. Eine neue allgemeine Darstellungsmethode der Aldehyde

Cited by 2 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. ChemInform Abstract: The Stereochemistry of the Grignard -Ortho Ester Reaction Revisited: Regioselective Endocyclic Cleavage in the Reaction of Grignard Reagents with cis-2-Methoxy-4-methyl-1,3-dioxane.;ChemInform;2010-08-03

2. Grignard Reactions of 4-Substituted-2-keto-1,3-dioxanes: Highly Diastereoselective Additions Controlled by a Remote Alkyl Group;Organic Letters;2001-05-18

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