Studies on heterocyclic analogs of azulenes. IV. Behavior of 2-chlorocyclohepta[b]pyrrole derivatives toward phosphorus ylide
Bulletin of the Chemical Society of Japan Volume 51 Issue 5
Page 1573-1574
published_at 1978
Title
Studies on heterocyclic analogs of azulenes. IV. Behavior of 2-chlorocyclohepta[b]pyrrole derivatives toward phosphorus ylide
The transylidation reaction of methyl(triphenylphosphoranylidene)acetate with 2-chlorocyclohepta[b]pyrrole derivatives has been studied. 3,8-Disubstituted derivatives gave a transylidation product only, whereas 3-substituted derivatives afforded not only a transylidation products but also the compounds formed by the addition of ylide at C-8. ^<13>C NMR spectra of the transylidation products are recorded in part.
Languages
eng
Resource Type
journal article
Publishers
日本化学会
Date Issued
1978
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）