Total Synthesis of (15R)- and (15S)-F2t-Isoprostanes by a Biomimetic Process Using the Cyclization of Acyclic Dihydroxylated Octa-5,7-dienyl Radicals

Article de revue

Thierry Durand, Alexandre Guy, Jean-Pierre Vidal et Jean-Claude Rossi

ChemInform, Vol.33(44), pp.226-226

05/11/2002

Résumé

diastereoselective syntheses

enantioselective syntheses (incl. ci/trans-isomerism)

hormones

1 Consultations de la notice

Titre: Total Synthesis of (15R)- and (15S)-F2t-Isoprostanes by a Biomimetic Process Using the Cyclization of Acyclic Dihydroxylated Octa-5,7-dienyl Radicals
Créateurs - sans rôle: Thierry Durand - Lab. Chim. Biomol. Interact. Biol., CNRS, Fac. Pharm., Univ. Montpellier I, F-34060 Montpellier, Fr
Alexandre Guy - Lab. Chim. Biomol. Interact. Biol., CNRS, Fac. Pharm., Univ. Montpellier I, F-34060 Montpellier, Fr
Jean-Pierre Vidal - Lab. Chim. Biomol. Interact. Biol., CNRS, Fac. Pharm., Univ. Montpellier I, F-34060 Montpellier, Fr
Jean-Claude Rossi - Lab. Chim. Biomol. Interact. Biol., CNRS, Fac. Pharm., Univ. Montpellier I, F-34060 Montpellier, Fr
Détails de publication: ChemInform, Vol.33(44), pp.226-226
Éditeur: Hüthig & Wepf Verlag
Nombre de pages: 1
Identifiants: 99138621509311
Unité académique: Institut des Biomolécules Max Mousseron - IBMM
Langue: English
Type de ressource: Journal article