Author:
Banwell Martin G.,Hockless David C. R.,Flynn Bernard L.,Longmore Robert W.,Rae David
Abstract
The 1,2,4-trisubstituted pyrrole (4), which is readily prepared from pyrrole
itself, undergoes double- barrelled Heck cyclizations to give,
inter alia, compounds (3) and (17) for which crystal
structures have been determined. Product (3) constitutes the core associated
with several key members, e.g. (1) and (2), of the lamellarin class of marine
alkaloid.
Cited by
52 articles.
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