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Issue 82, 2012
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Diastereoselective synthesis of half-sandwich chiral-at-metal cobaltacycles by oxidative cyclisation

Jahangir Amina  and  Christopher J. Richards*a 
Author affiliations

* 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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Publication details

The article was received on 06 Jul 2012, accepted on 09 Aug 2012 and first published on 10 Aug 2012


Article type: Communication
DOI: 10.1039/C2CC34837C
Citation: Chem. Commun., 2012,48, 10192-10194
  • Open access: Creative Commons BY license
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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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