A domino ring-closing metathesis as a key-step in the synthesis of chiral lactones from D-mannitol. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Tetrahedron Letters Année : 2005

A domino ring-closing metathesis as a key-step in the synthesis of chiral lactones from D-mannitol.

Résumé

Chiral lactones were synthesized in six steps from d-mannitol. The key-step was a domino ring-closing metathesis reaction leading to the symmetric cleavage of a d-mannitol triene derivative and to the formation of two molecules of the desired lactone.

Dates et versions

hal-00086259 , version 1 (18-07-2006)

Identifiants

Citer

Bastien Nay, Nicolas Gaboriaud-Kolar, Bernard Bodo. A domino ring-closing metathesis as a key-step in the synthesis of chiral lactones from D-mannitol.. Tetrahedron Letters, 2005, 46 (22), pp.3867-3870. ⟨10.1016/j.tetlet.2005.03.189⟩. ⟨hal-00086259⟩

Collections

MNHN CNRS
54 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More