An efficient and stereoselective construction of the core structure of the manzamines via an intramolecular Michael reaction

DOI: 10.1016/S0040-4039(98)00019-7

Source and publish data:

Tetrahedron Letters p. 1677 - 1680 (1998)

Update date:2022-07-30

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Brands Brands

DiMichele

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Article abstract of DOI:10.1016/S0040-4039(98)00019-7

A strategically functionalized tricyclic subunit of the manzamines was efficiently synthesized with complete stereochemical control using a combination of an intramolecular Michael reaction of a pyroglutamic acid derivative and a hydrogenation.

Full text of DOI:10.1016/S0040-4039(98)00019-7

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