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Carene terpenoids by gold-catalyzed cycloisomerization reactions

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Fürstner,  Alois
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Hannen,  Peter
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

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


Cite as: http://hdl.handle.net/11858/00-001M-0000-000F-96CB-B
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.