Superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether

Academic Article
Publication Date:
2000
abstract:
The superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether 2 begins at the internal double bond giving a mixture of diastereomeric monocyclic compounds 5 and 6, prenylated at gem-dimethyl groups.
Iris type:
01.01 Articolo in rivista
Keywords:
cyclizations; superacids; terpenoids; carbocations
List of contributors:
Authors of the University:
Handle:
https://iris.cnr.it/handle/20.500.14243/426973
Published in:
SYNTHESIS (STUTTG.)
Journal