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  Construction of Tetracyclic Indole Bases Via Aza-Diels-Alder Reaction of Indolylethylimines with Brassard's Diene

Lock, R., & Waldmann, H. (1993). Construction of Tetracyclic Indole Bases Via Aza-Diels-Alder Reaction of Indolylethylimines with Brassard's Diene. Natural Product Letters, 2(1), 49-56. doi:10.1080/10575639308043454.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9D0C-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-9D0D-2
Genre: Journal Article

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 Creators:
Lock, Ralf1, Author
Waldmann, Herbert2, Author           
Affiliations:
1External Organizations, ou_persistent22              
2Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753290              

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Free keywords: Aza-Diels-Alder reaction, Bischler-Napieralski reaction, Brassard's diene, indolo[2,3-a]quinolizines
 Abstract: Schiff bases derived from tryptamine react with Brassard's diene in the presence of EtAlCl2 to give functionalised 1,2,5,6-tetrahydropyridines which are subsequently transformed to indolo[2,3-a]quinolizines by Bischler-Napieralski reaction and reduction of the intermediate iminium salts with NaBH4.

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 Dates: 2006-10-041993
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1080/10575639308043454
 Degree: -

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Title: Natural Product Letters
Source Genre: Journal
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Publ. Info: Chur : Harwood Academic Publishers
Pages: - Volume / Issue: 2 (1) Sequence Number: - Start / End Page: 49 - 56 Identifier: ISSN: 1057-5634
CoNE: https://pure.mpg.de/cone/journals/resource/111054316638012_1