Asymmetric Oxidation of Silyl Enol Ethers Using Chiral Dioxiranes derived from α-Fluoro Cyclohexanones

Autor: Arlette Solladié-Cavallo, Roberto Antonioletti, Paolo Bovicelli, Arlette Klein, Paolo Lupattelli, F. Angeli, Loïc Jierry

Publikováno v: Tetrahedron letters 44 (2003): 6523–6526. doi:10.1016/S0040-4039(03)01388-1
info:cnr-pdr/source/autori:Solladie-Cavallo, A.; Lupattelli, P.; Jierry, L.; Bovicelli, P.; Angeli, F.; Antonioletti, R.; Klein, A./titolo:Asymmetric oxidation of silyl enol ethers using chiral dioxiranes derived from a-fluoro cyclohexanones/doi:10.1016%2FS0040-4039(03)01388-1/rivista:Tetrahedron letters/anno:2003/pagina_da:6523/pagina_a:6526/intervallo_pagine:6523–6526/volume:44

Asymmetric oxidation of silyl enolethers derived from tetralone, 2-methyl-tetralone, propiophenone and deoxybenzoin using chiral dioxiranes generated in situ from oxone and new chiral α-fluorinated cyclohexanones or fructose-derived ketone have been

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d24e4957fad6fc34491e338de675b988
http://hdl.handle.net/11573/1653050