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

Kirschbaum, S; Waldmann, Herbert

doi:10.1016/S0040-4039(97)00494-2

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

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Waldmann, Herbert
Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Citation

Kirschbaum, S., & Waldmann, H. (1997). Construction of the tricyclic benzoquinolizine ring system by combination of a tandem Mannich-Michael reaction with a Heck reaction. TETRAHEDRON LETTERS, 38(16), 2829-2832. doi:10.1016/S0040-4039(97)00494-2.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-71E3-B

Abstract

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. (C) 1997 Elsevier Science Ltd.