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

Authors
WINKLER JD SIEGEL MG STELMACH JE
Citation
Jd. Winkler et al., A HIGHLY STEREOSELECTIVE APPROACH TO THE SYNTHESIS OF THE MANZAMINE ALKALOIDS VIA THE INTRAMOLECULAR VINYLOGOUS AMIDE PHOTOCYCLOADDITION, Tetrahedron letters, 34(41), 1993, pp. 6509-6512
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
41
Year of publication
1993
Pages
6509 - 6512
Database
ISI
SICI code
0040-4039(1993)34:41<6509:AHSATT>2.0.ZU;2-T
Abstract
The stereoselective construction of the tetracyclic core of the manzam ine alkaloids via the intramolecular vinylogous amide photocycloadditi on/retro-Mannich fragmentation/Mannich closure sequence using an eight -membered ring template is described.