Author:
Purdy John,McLean Stewart
Abstract
The aglucone of sweroside has been converted to naucledal and its epimer, 3-epinaucledal; the structure and stereochemistry of these products have been established through analysis of their nmr spectra. The course of the rearrangement has been studied and the intermediacy of a ring–opened isomer, seconaucledal, has been demonstrated. The relative amounts of naucledal and 3-epinaucledal produced from seconaucledal depend on the conditions of the cyclization.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
11 articles.
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