Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization) - Archive ouverte HAL
Article Dans Une Revue Tetrahedron: Asymmetry Année : 2010

Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization)

Résumé

The chiral cyclosulfamide (S)-2-benzyl-4-isopropyl-1,2,5-thiadiazolidine 1,1-dioxide was designed as a chimera of Evans and Oppolzer chiral auxiliaries. The N-propionyl derivative appeared to be very powerful for the stereocontrolled synthesis of chiral building blocks through asymmetric aldolization and alkylation reactions.

Dates et versions

hal-00533621 , version 1 (08-11-2010)

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Citer

Fabien Fécourt, Gérald Lopez, Arie van Der Lee, Jean Martinez, Georges Dewynter. Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization). Tetrahedron: Asymmetry, 2010, 21, pp.2361-2366. ⟨10.1016/j.tetasy.2010.09.001⟩. ⟨hal-00533621⟩
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