Issue 18, 2002

A chemo- and stereoselective reduction of cycloalkynes to (E)-cycloalkenes

Abstract

A stereoselective entry into (E)-cycloalkenes is described, comprising the ring closing alkyne metathesis (RCAM) of suitable diynes, a ruthenium-catalyzed trans-selective hydrosilylation of the cycloalkynes thus formed, followed by a desilylation of the resulting vinylsilanes mediated by AgF.

Graphical abstract: A chemo- and stereoselective reduction of cycloalkynes to (E)-cycloalkenes

Article information

Article type
Communication
Submitted
24 Jul 2002
Accepted
14 Aug 2002
First published
28 Aug 2002

Chem. Commun., 2002, 2182-2183

A chemo- and stereoselective reduction of cycloalkynes to (E)-cycloalkenes

A. Fürstner and K. Radkowski, Chem. Commun., 2002, 2182 DOI: 10.1039/B207169J

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