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  CONSTRUCTION OF TETRACYCLIC INDOLE BASES VIA AZA-DIELS-ALDER REACTION OF INDOLYLETHYLIMINES WITH BRASSARD DIENE

LOCK, R., & Waldmann, H. (1994). CONSTRUCTION OF TETRACYCLIC INDOLE BASES VIA AZA-DIELS-ALDER REACTION OF INDOLYLETHYLIMINES WITH BRASSARD DIENE. LIEBIGS ANNALEN DER CHEMIE, (5), 511-516.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-72A8-9 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9A65-1
Genre: Journal Article

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 Creators:
LOCK, R1, 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: ACID ESTER IMINES; ALKALOIDS; INDOLO<2,3-A>QUINOLIZIDIN-2-ONES; DIELS-ALDER REACTIONS; BISCHLER-NAPIERALSKI REACTIONS; BRASSARDS DIENE; INDOLO[2,3-A]QUINOLIZINES; ALKALOIDS;
 Abstract: Schiff's bases 3 derived from tryptamine react with Brassard's diene 4 in the presence of EtAlCl2 to give functionalized 1,2,5,6-tetrahydropyridines which are subsequently transformed to indolo[2,3-a]quinolizines 8-10 by the Bischler-Napieralski reaction and reduction of the intermediate iminium salts with NaBH4.

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Language(s): eng - English
 Dates: 1994-05
 Publication Status: Issued
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: A1994NR91200010
 Degree: -

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Title: LIEBIGS ANNALEN DER CHEMIE
Source Genre: Journal
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Publ. Info: Weinheim : VCH
Pages: - Volume / Issue: (5) Sequence Number: - Start / End Page: 511 - 516 Identifier: ISSN: 0170-2041