Issue 82, 2012
From the journal:

Chemical Communications

Diastereoselective synthesis of half-sandwich chiral-at-metal cobaltacycles by oxidative cyclisation†

Jahangir Amina  and  Christopher J. Richards*a  

* Corresponding authors

a School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, UK
E-mail: Chris.Richards@uea.ac.uk
Fax: +44 (0)1603 592003
Tel: +44 (0)1603 592003

Abstract

Reaction of chiral ester linked diynes with chlorotris(triphenylphosphine)cobalt(I) and sodium cyclopentadienide gave (η5-cyclopentadienyl)(triphenylphosphine) cobaltacyclopentadiene complexes as single chiral-at-metal diastereoisomers, including a non-racemic example synthesised in three steps from (S)-3-butyn-2-ol.

Graphical abstract: Diastereoselective synthesis of half-sandwich chiral-at-metal cobaltacycles by oxidative cyclisation

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Article information

DOI
https://doi.org/10.1039/C2CC34837C
Article type
Communication
Submitted
06 Jul 2012
Accepted
09 Aug 2012
First published
10 Aug 2012
This article is Open Access
Creative Commons BY license

Chem. Commun., 2012,48, 10192-10194

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Diastereoselective synthesis of half-sandwich chiral-at-metal cobaltacycles by oxidative cyclisation

J. Amin and C. J. Richards, Chem. Commun., 2012, 48, 10192 DOI: 10.1039/C2CC34837C

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