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

โœ Scribed by Robert M Williams; Tomasz Glinka

Book ID
104218934
Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
189 KB
Volume
27
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

An effective intramolecular Michael cyclization and intramolecular SN2' cyclization is described for constructing the tricyclic framework of the natural mycotoxins brevianamides A,B. Brevianamides A,B (1) have been isolated' from several species of Penicillium associated with corn, rice and other stored grains subject to growth of molds and fungi. Birchla and his

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