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  Concise total syntheses of epothilone A and C based on alkyne metathesis

Fürstner, A., Mathes, C., & Grela, K. (2001). Concise total syntheses of epothilone A and C based on alkyne metathesis. Chemical Communications, (12), 1057-1059. doi:10.1039/B101669P.

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 Creators:
Fürstner, Alois1, Author           
Mathes, Christian1, Author           
Grela, Karol1, Author
Affiliations:
1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: A ring closing alkyne metathesis reaction catalyzed by the molybdenum complex 26 followed by a Lindlar reduction of the resulting cycloalkyne product opens an efficient and stereoselective entry into epothilone A and C.

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Language(s): eng - English
 Dates: 2001-02-202001-05-082001-05-252001
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/B101669P
 Degree: -

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Title: Chemical Communications
  Other : Chem. Commun.
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: 3 Volume / Issue: (12) Sequence Number: - Start / End Page: 1057 - 1059 Identifier: ISSN: 1359-7345
CoNE: https://pure.mpg.de/cone/journals/resource/954928495413