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Promising cyclization reactions to construct the ring systems of brevianamides A,B

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
27
Issue
31
Identifiers
DOI: 10.1016/s0040-4039(00)84854-6

Abstract

Intramolecular Michael cyclization and intramolecular SN 2′ cyclization of 1 and 2 furnishes the tricyclic frameworks 3 4 and 5 respectively of the natural mycotoxins brevianamides A,B.

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