Diastereoface differentiating peracid oxidation of the enol ether derived from cyclohexanone and 2,4-pentanediol: Preparation of optically pure 2-hydroxycyclohexanone acetal-Reference-Cited by-同舟云学术

Diastereoface differentiating peracid oxidation of the enol ether derived from cyclohexanone and 2,4-pentanediol: Preparation of optically pure 2-hydroxycyclohexanone acetal

Published:1993-01 Issue:1 Volume:4 Page:43-44
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Sugimura Takashi,Nishiyama Norio,Tai Akira,Hakushi Tadao

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference9 articles.

1. Diastereo-differentiating simmons-smith reaction using 2,4-pentanediol as a chiral auxiliary

2. Diastereo-differentiating cyclopropanation of a chiral enol ether: a simple method for the preparation of optically pure cyclopropyl ethers

3. Asymmetric functionalization of conformationally distinctive Cs-symmetric cis-[n.3.1] bicyclic ketones. Definition of the absolute course of enantio- and diastereodifferentiation

4. Epoxyethers. IV. Mechanism of the Opening of an Epoxyether with an Organic Acid1

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