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
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
[isVersionOf]
[URI]http://www.rsc.org/Publishing/Journals/P1/Index.asp
Schools
大学院医学系研究科（理学）