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  Syntheses of Camalexin, Indolopyridocoline and Flavopereirine

Fürstner, A., & Ernst, A. (1995). Syntheses of Camalexin, Indolopyridocoline and Flavopereirine. Tetrahedron, 51(3), 773-786. doi:10.1016/0040-4020(94)00987-6.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-A485-C Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0019-F919-3
Genre: Journal Article

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 Creators:
Fürstner, Alois1, Author           
Ernst, Andreas1, Author           
Affiliations:
1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: A short synthetic route to the phytoalexin camalexin 7 and a convergent approach to the alkaloids indolopyridocoline 8, 6,7-dihydroflavopereirine 15 and flavopereirine 9 are presented. Starting from well accessible precursors, these total syntheses highlight the preparative potential of a new method for indole synthesis based on the formation of the C2-C3 bond by low-valent titanium induced reductive coupling of oxo-amides.

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Language(s): eng - English
 Dates: 1994-10-211994-11-041995-01-16
 Publication Status: Issued
 Pages: 14
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/0040-4020(94)00987-6
 Degree: -

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Title: Tetrahedron
  Other : Tetrahedron
Source Genre: Journal
 Creator(s):
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Publ. Info: Oxford : Pergamon
Pages: 14 Volume / Issue: 51 (3) Sequence Number: - Start / End Page: 773 - 786 Identifier: ISSN: 0040-4020
CoNE: https://pure.mpg.de/cone/journals/resource/954925448773