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）