PROMISING CYCLIZATION REACTIONS TO CONSTRUCT THE RING SYSTEMS OF BREVIANAMIDES A,B

DOI: 10.1016/S0040-4039(00)84854-6

Source and publish data:

Tetrahedron Letters p. 3581 - 3584 (1986)

Update date:2022-08-04

Topics:

Authors:

Williams, Robert M.

Glinka, Tomasz

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Article abstract of DOI:10.1016/S0040-4039(00)84854-6

An effective intramolecular Michael cyclization and intramolecular SN₂'cyclization is described for constructing the tricyclic framework of the natural mycotoxins brevianamides A,B.

Full text of DOI:10.1016/S0040-4039(00)84854-6

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