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.
Superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether
Castelluccio F;Cimino G
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.File in questo prodotto:
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