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Abe Noritaka

Affiliate Master Yamaguchi University

Studies of heterocyclic analogues of azulenes. Part 9. Regioselective cycloadditions of 2H-cycloheptathiazol-2-one with acetylenic esters and electron-deficient olefins

Journal of the Chemical Society. Perkin transactions 1 : organic and bio-organic chemistry Volume 1982 Page 2881-2883
published_at 1982
Title
Studies of heterocyclic analogues of azulenes. Part 9. Regioselective cycloadditions of 2H-cycloheptathiazol-2-one with acetylenic esters and electron-deficient olefins
Creators Abe Noritaka
Creators Nishiwaki Tarozaemon
Creators Shigematsu Mitsuharu
Cycloadditions of 2H-cycloheptathiazol-2-one with acetylenic esters and electron-deficient olefins have been found to proceed regioselectively, producing 2-oxo-3H-1-this-2a-azacyclopent[cd]azulenes by 1,10-dipolar cyclisation, and 2-oxo-3H-1-this-2a-azacyclopenta[ef]heptalenes.
Languages eng
Resource Type journal article
Publishers Royal Society of Chemistry
Date Issued 1982
File Version Not Applicable (or Unknown)
Access Rights metadata only access
Relations
[ISSN]0300-922X
[NCID]AA00695134
info:doi/10.1039/P19820002881
[isVersionOf] [URI]http://www.rsc.org/Publishing/Journals/P1/Index.asp
Schools 大学院医学系研究科(理学)