Switchable Diastereoselectivity in the Fluoride-Promoted Vinylogous Mukaiyama–Michael Reaction of 2-[(Trimethylsilyl)oxy]furan Catalyzed by Crown Ethers

Frédéric R. Leroux (1) , Giorgio Della Sala , Marina Sicignano , Rosaria Schettini , Francesco de Riccardis (2) , Luigi Cavallo (3) , Yury Minenkov (4) , Chloé Batisse (1) , Gilles Hanquet (1) , Irene Izzo

1 LIMA - Laboratoire d'innovation moléculaire et applications
2 UNISA - Università degli Studi di Salerno = University of Salerno
3 Dipartimento di Ingegneria Chimica e Alimentare (Salerno, Italy)
4 KAUST - Division of Physical Sciences and Engineering (KAUST)

Domaines: Chimie organique

Frédéric R. Leroux, Giorgio Della Sala, Marina Sicignano, Rosaria Schettini, Francesco de Riccardis, et al.. Switchable Diastereoselectivity in the Fluoride-Promoted Vinylogous Mukaiyama–Michael Reaction of 2-[(Trimethylsilyl)oxy]furan Catalyzed by Crown Ethers. Journal of Organic Chemistry, 2017, 82 (13), pp.6629-6637. ⟨10.1021/acs.joc.7b00743⟩. ⟨hal-02105791⟩