DIPOLAR CYCLOADDITIONS OF SEVERAL MESOIONIC COMPOUNDS WITH TERT-BUTYLFULVENE DERIVATIVES - VERSATILE REACTIONS, STERICALLY CONTROLLED [4-PI-PI] CYCLOADDITIONS AND A NEW ROUTE TO HETEROCYCLES ISOELECTRONIC WITHAZULENE(6)

Authors
KATO H KOBAYASHI T CIOBANU M IGA H AKUTSU A KAKEHI A
Citation
H. Kato et al., DIPOLAR CYCLOADDITIONS OF SEVERAL MESOIONIC COMPOUNDS WITH TERT-BUTYLFULVENE DERIVATIVES - VERSATILE REACTIONS, STERICALLY CONTROLLED [4-PI-PI] CYCLOADDITIONS AND A NEW ROUTE TO HETEROCYCLES ISOELECTRONIC WITHAZULENE(6), Chemical communications, (9), 1996, pp. 1011-1012
Citations number
7
Categorie Soggetti
Chemistry
Journal title
Chemical communications → ACNP
ISSN journal
13597345
Issue
9
Year of publication
1996
Pages
1011 - 1012
Database
ISI
SICI code
1359-7345(1996):9<1011:DCOSMC>2.0.ZU;2-0
Abstract
Several mesoionic compounds react with 2-tert-butylfulvene derivatives to form [4 pi + 2 pi] and [4 pi + 6 pi] cycloadducts, which under the reaction conditions, undergo further fragmentation, elimination, or i somerization giving a variety of products including several condensed heterocycles which are isoelectronic with azulene.