Photochemical reactions of 3-acyl-2-thiotetrahydro-1,3-thiazines; a new synthesis of cepham analogues-Reference-Cited by-同舟云学术

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Photochemical reactions of 3-acyl-2-thiotetrahydro-1,3-thiazines; a new synthesis of cepham analogues

Published:1986-01 Issue:12 Volume:27 Page:1335-1338
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sakamoto Masami,Aoyama Hiromu,Omote Yoshimori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Photochemical reactions of .alpha.-oxo amides. Norrish type II reactions via zwitterionic intermediates

2. A new synthesis of .beta.-lactams: 3-oxo-6-thia-2-azabicyclo[2.2.0]hexanes via photochemical reactions of N-(thiobenzoyl)methacrylamides

3. β-Lactams via photochemical reaction of monothioimides

4. Photochemical activation of the carboxyl group via n-acyl-2-thionothiazolidines

5. Nonconcerted cycloreversion by electron impact of substituted 2,4-azetidinediones. Relations between the mass spectral and photochemical reactions

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1. Photo-reorganization of 3-alkoxy-6-chloro-2-(thiophen-3-yl)-4H-chromen-4-ones: Regioselective cyclization via γ-hydrogen abstraction;Journal of Photochemistry and Photobiology A: Chemistry;2011-05

2. Volume 6 References;Comprehensive Heterocyclic Chemistry II;1996

3. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996

4. 1,3-Thiazines and their Benzo Derivatives;Comprehensive Heterocyclic Chemistry II;1996

5. Azetidines, Azetines, and Azetes: Monocyclic;Comprehensive Heterocyclic Chemistry II;1996

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