Enantioselective alkylative double ring opening of epoxides: synthesis of enantioenriched unsaturated diols and amino alcohols.

Enantioselective generation and intermolecular trapping of a lithium carbenoid occurs in the reaction of epoxides of 2,5-dihydrofuran, 2,5-dihydropyrrole, and oxa- and aza-bicyclo[n.2.1]alkenes (n = 2, 3) with organolithium compounds in the presence of external chiral ligands. This methodology leads...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Hodgson, D, Maxwell, C, Miles, T, Paruch, E, Stent, M, Matthews, I, Wilson, F, Witherington, J
Format: Journal article
Język:English
Wydane: 2002