Synthesis 2001(12): 1888-1896
DOI: 10.1055/s-2001-17511
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© Georg Thieme Verlag Stuttgart · New York

Asymmetric Pauson-Khand Cyclizations of 1-Sulfinylenynes

Juan Carlos Carretero*, Javier Adrio
a Departamento de Química Orgánica, Facultad de Ciencias, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain
Fax: +34(9)13973925; e-Mail: juancarlos.carretero@uam.es;
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Publikationsverlauf

Received 21 May 2001
Publikationsdatum:
11. August 2004 (online)

Abstract

The use of sulfoxides as chiral auxiliaries in intramolecular Pauson-Khand (PK) reactions is described. In particular, the tert-butylsulfinyl group acts as a very efficient chiral auxiliary in intramolecular PK reactions of 1-sulfinyl-1,6-enynes. As the starting enynes are readily available in optically pure form and the final desulfinylation step is high yielding, this procedure constitutes an efficient alternative to the synthesis of enantiomerically pure bicyclo[3.3.0]oct-1-en-3-ones.

    References

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9

The o-(N,N-dimethylamino)phenylsulfinyl group has been used as an efficient chiral auxiliary in asymmetric Heck reactions, see ref. [5] .

10

The crystallographic data of compound 4cA have been deposited at the Cambridge Crystallographic Data Centre (supplementary publication nº CCDC 133957); see also ref. [7] .