Preparation of the laevorotatory trans-(4S,6S)-4,6-dimethyl-1,3-dithiane and trans-(4S,6S)-4,6-dimethyl-1,3-oxathiane. An internal displacement of a secondary sulphonate leading to a cyclic thioacetal-Reference-Cited by-同舟云学术

Preparation of the laevorotatory trans-(4S,6S)-4,6-dimethyl-1,3-dithiane and trans-(4S,6S)-4,6-dimethyl-1,3-oxathiane. An internal displacement of a secondary sulphonate leading to a cyclic thioacetal

Published:1975-01 Issue:4 Volume:31 Page:327-331
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Danneels D.,Anteunis M.,van Acker L.,Tavernier D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. NMR-experiments on Acetals: XXII [1]. Conformational Equilibria in Trans-4,6-Disubstituted-1,3-Thioxanes

2. NMR-Experiments on Acetals: XXIII The Ring Shape of m-Dioxanes, m-Dithianes and m-Thioxanes

3. Conformational analysis. XVIII. 1,3-Dithianes. Conformational preferences of alkyl substituents and the chair-boat energy difference

4. Asymmetric Hydrogenation with Modified Raney Nickel. II. Studies on Modified Hydrogenation Catalyst. III

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