ChemInform Abstract: Highly Diastereoselective 1,6-Conjugate Addition of Arylboronic Acids to Securinine

Article de revue

Marc Perez, Tahar Ayad, Philippe Maillos, Valerie Poughon, Jacques Fahy et Virginie Ratovelomanana-Vidal

ChemInform, Vol.47(35), pp.no-no

01/08/2016

Résumé

Acids

Rhodium catalysis provides access to the single diastereomers of the regioselective C15-arylation products of securinine in good yields.

1 Consultations de la notice

Titre: ChemInform Abstract: Highly Diastereoselective 1,6-Conjugate Addition of Arylboronic Acids to Securinine
Créateurs - sans rôle: Marc Perez
Tahar Ayad
Philippe Maillos
Valerie Poughon
Jacques Fahy
Virginie Ratovelomanana-Vidal
Détails de publication: ChemInform, Vol.47(35), pp.no-no
Éditeur: Wiley Subscription Services, Inc
Identifiants: 99158439409311
Unité académique: Institut Charles Gerhardt Montpellier - ICGM
Langue: English
Type de ressource: Journal article