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Bildung tricyclischer Thietan-Derivate durch intramolekulare (2+2)-Cycloaddition


Wipf, Peter; Heimgartner, Heinz (1987). Bildung tricyclischer Thietan-Derivate durch intramolekulare (2+2)-Cycloaddition. Helvetica Chimica Acta, 70:992-994.

Abstract

On irradiation, the two 4-vinyl-1,3-thiazole-5(4H)-thiones 1a, b, synthesized from thiobenzoic acid and the corresponding 3-amino-2H-azirines 2a, b, undergo an intramolecular (2+2)-cycloaddition reaction of the C=S and C=C bonds to give the tricyclic thietane derivatives 3a, b.

On irradiation, the two 4-vinyl-1,3-thiazole-5(4H)-thiones 1a, b, synthesized from thiobenzoic acid and the corresponding 3-amino-2H-azirines 2a, b, undergo an intramolecular (2+2)-cycloaddition reaction of the C=S and C=C bonds to give the tricyclic thietane derivatives 3a, b.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
Dewey Decimal Classification:540 Chemistry
Language:German
Date:1987
Deposited On:21 May 2014 14:42
Last Modified:05 Apr 2016 17:52
Publisher:Wiley-Blackwell
ISSN:0018-019X
Funders:Schweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung, F. Hoffmann-La Roche & Co. AG, Basel
Permanent URL: https://doi.org/10.5167/uzh-95991

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