A HIGHLY STEREOSELECTIVE APPROACH TO THE SYNTHESIS OF THE MANZAMINE ALKALOIDS VIA THE INTRAMOLECULAR VINYLOGOUS AMIDE PHOTOCYCLOADDITION

DOI: 10.1016/0040-4039(93)88091-V

Source and publish data:

Tetrahedron Letters p. 6509 - 6512 (1993)

Update date:2022-08-05

Topics:

Authors:

Winkler, Jeffrey D.

Siegel, Miles G.

Stelmach, John E.

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Article abstract of DOI:10.1016/0040-4039(93)88091-V

The stereoselective construction of the tetracyclic core of the manzamine alkaloids via the intramolecular vinylogous amide photocycloaddition/retro-Mannich fragmentation/Mannich closure sequence using an eight-membered ring template is described.

Full text of DOI:10.1016/0040-4039(93)88091-V

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