Construction of the tricyclic benzoquinolizine ring system by combination of a tandem Mannich-Michael reaction with a Heck reaction

Tetrahydro- and hexahydrobenzo[a]quinolizinones can be built up efficiently by means of a two step reaction sequence consisting of a tandem Mannich-Michael reaction and a Heck reaction. Graphic

Saved in:
Bibliographic Details
Published inTetrahedron letters Vol. 38; no. 16; pp. 2829 - 2832
Main Authors Kirschbaum, Stephan, Waldmann, Herbert
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 21.04.1997
Elsevier
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
TETRACYCLIC INDOLE BASES
BRASSARD DIENE
CATALYZED REACTIONS
INDOLYLETHYLIMINES
YOHIMBINE-TYPE ALKALOIDS
IMINES
DIELS-ALDER REACTION
DERIVATIVES
CYCLIZATION
Online AccessGet full text

Cover

More Information
Summary:Tetrahydro- and hexahydrobenzo[a]quinolizinones can be built up efficiently by means of a two step reaction sequence consisting of a tandem Mannich-Michael reaction and a Heck reaction. Graphic
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(97)00494-2