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Article Dans Une Revue Tetrahedron Letters Année : 2007

Diastereoselective Michael additions to α,β-unsaturated α-sulfinyl phosphonates in the thiolane series

Résumé

A chiral racemic 2-phosphono-2,3-didehydrothiolane sulfoxide was used as a Michael acceptor in the reactions with several nucleophiles, in particular thiols. In most cases the reactions were fully diastereoselective. The relative configuration of the resulting adducts was determined.

Dates et versions

hal-01581424 , version 1 (04-09-2017)

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Piotr Łyżwa, Aleksandra Jankowiak, Małgorzata Kwiatkowska, Marian Mikołajczyk, Piotr Kiełbasiński, et al.. Diastereoselective Michael additions to α,β-unsaturated α-sulfinyl phosphonates in the thiolane series. Tetrahedron Letters, 2007, 48 (3), pp.351 - 355. ⟨10.1016/j.tetlet.2006.11.098⟩. ⟨hal-01581424⟩
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