Authors: E V Kuzakov É N Shmidt
Publish Date: 2013/10/23
Volume: 34, Issue: 5, Pages: 594-601
Abstract
The alkylation of some phenols with an allyl 6oxolabdane alcohol in the presence of the clay askanitebentonite has been investigated It has been shown that during the reaction intermediateortho adducts of substitution in the aromatic nucleus are cyclized into chroman derivatives containing a bicyclic terpene residue —2methyl26′oxoδτtetranorlabd12′ylchromans Performing the reaction in the presence of heterogeneous catalysts imposes limitations on the yields of certain productsNovosibirsk Institute of Organic Chemistry Siberian Division of the Russian Academy of Sciences Novosibirsk fax 83832 3 54 752 email shreerdniochnscru Translated from Khimiya Prirodnykh Soedinenii No 5 pp 653–662 September–October 1998
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