Rearrangements in the 11-Thia-9,10-dihydro-9,10-ethanoanthracene Series. Synthesis of a Bridged Thienooxepin-Reference-Cited by-同舟云学术

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Rearrangements in the 11-Thia-9,10-dihydro-9,10-ethanoanthracene Series. Synthesis of a Bridged Thienooxepin

Published:1999-02 Issue:2 Volume:23 Page:166-167
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Minassian Frédéric¹,Pelloux-Léon Nadia¹,Averbuch-Pouchot Marie-Thérèse¹,Vallée Yannick¹

Affiliation:

1. LEDSS, UMR CNRS 5616 - Université Joseph Fourier, Domaine Universitaire, BP 53, 38041 Grenoble, France

Abstract

A rearrangement from 11-thia-9,10-dihydro-9,10-ethanoanthracene derivatives into a thienooxepin is reported; the structure of the bridged oxepin is confirmed by X-ray analysis.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.1177/174751989902300250

Reference8 articles.

1. Pelloux-LéonN., and ValléeY., in Gas Phase Reactions in Organic Synthesis, ed. ValléeY., Gordon and Breach Science Publishers, 1997, p. 275.

2. Sulfur (Or Selenium)-Mediated Synthesis of Methanoanthracene Derivatives. The First Synthesis of a Seleno-Cyanohydrin

3. In search for thioketene S-oxide. A vinyl sulfoxide to sulfine rearrangement

4. Theoretical study of the cyclization of α-iminothioaldehydes into dihydrothiazoles

5. New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

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