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  Carene terpenoids by gold-catalyzed cycloisomerization reactions

Fürstner, A., & Hannen, P. (2004). Carene terpenoids by gold-catalyzed cycloisomerization reactions. Chemical Communications, (22), 2546-2547. doi:10.1039/B412354A.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-96CB-B Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0028-1401-9
Genre: Journal Article

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 Creators:
Fürstner, Alois1, Author           
Hannen, Peter1, Author           
Affiliations:
1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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 Abstract: Propargyl acetates in the presence of catalytic amounts of AuCl3 constitute synthetic equivalents of α-diazoketones as illustrated by a concise entry into the carene family of natural products.

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Language(s): eng - English
 Dates: 2004-08-102004-09-062004-10-062004
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 218327
DOI: 10.1039/B412354A
ISI: 000225375100012
 Degree: -

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Title: Chemical Communications
  Other : Chem. Commun.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: (22) Sequence Number: - Start / End Page: 2546 - 2547 Identifier: ISSN: 1359-7345
CoNE: https://pure.mpg.de/cone/journals/resource/954928495413