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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 Abe Noritaka
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
https://doi.org/10.1246/bcsj.53.1773
[isPartOf] [URI]http://www.jstage.jst.go.jp/browse/bcsj/-char/en
Schools 大学院医学系研究科(理学)