Cycloalkylation d'aryloléfines par le trifluorure de bore. Synthèse d'hydrocarbures aromatiques polyméthylés
Open Access
- 1 August 1969
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 47 (15) , 2837-2842
- https://doi.org/10.1139/v69-470
Abstract
A survey of the results obtained by us in the course of cyclizations of 4-arylolefins indicates that boron trifluoride is the most satisfactory catalyst in the case of otherwise non-functionalized substrates. Its use is illustrated by the synthesis of the heretofore unknown 1,3,6,8-tetramethyltriphenylene and by an improved preparation of 1,5-dimethylnaphthalene.Keywords
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