Studies on Heterocyclic Analogs of Azulene. VII. : Regioselective Cycloadditions of Cycloheptimidazole to Electron-deficient Olefins
Bulletin of the Chemical Society of Japan Volume 53 Issue 6
Page 1773-1774
published_at 1980
Title
Studies on Heterocyclic Analogs of Azulene. VII. : Regioselective Cycloadditions of Cycloheptimidazole to Electron-deficient Olefins
Creators
Nishiwaki Tarozaemon
Cycloheptimidazole reacted with electrondeficient olefins (e.g., ethyl acrylate or acrylonitrile) to give the regioselective [6+2] cycloadducts, which were readily dehydrogenated to give 2a,3-dihydro-1,2a-diazacyclopent[cd]azulenes.
Languages
eng
Resource Type
journal article
Publishers
日本化学会
Date Issued
1980
File Version
Not Applicable (or Unknown)
Access Rights
metadata only access
Relations
[ISSN]0009-2673
[NCID]AA00580132
[isPartOf]
[URI]http://www.jstage.jst.go.jp/browse/bcsj/-char/en
Schools
大学院医学系研究科（理学）