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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-71E3-B Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-7282-E
Genre: Journal Article

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 Creators:
Kirschbaum, S1, Author
Waldmann, Herbert2, Author           
Affiliations:
1external, ou_persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: TETRACYCLIC INDOLE BASES; YOHIMBINE-TYPE ALKALOIDS; DIELS-ALDER REACTION; CATALYZED REACTIONS; BRASSARD DIENE; INDOLYLETHYLIMINES; DERIVATIVES; CYCLIZATION; IMINES
 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.

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Language(s): eng - English
 Dates: 1997
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: A1997WV21200013
DOI: 10.1016/S0040-4039(97)00494-2
 Degree: -

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Title: TETRAHEDRON LETTERS
Source Genre: Journal
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Publ. Info: KIDLINGTON, OXFORD : PERGAMON-ELSEVIER SCIENCE
Pages: - Volume / Issue: 38 (16) Sequence Number: - Start / End Page: 2829 - 2832 Identifier: ISSN: 0040-4039