Artículos de revistas
Chemo-, Regio- And Stereoselective Heck Arylation Of Allylated Malonates: Mechanistic Insights By Esi-ms And Synthetic Application Toward 5-arylmethyl-γ-lactones.
Registro en:
Organic Letters. v. 16, n. 19, p. 5180-3, 2014-Oct.
1523-7052
10.1021/ol502529v
25247735
Autor
Oliveira, Caio C
Marques, Marcelo V
Godoi, Marla N
Regiani, Thaís
Santos, Vanessa G
dos Santos, Emerson A F
Eberlin, Marcos N
Sá, Marcus M
Correia, Carlos R D
Institución
Resumen
We describe herein a general method for the controlled Heck arylation of allylated malonates. Both electron-rich and electron-poor aryldiazonium salts were readily employed as the aryl-transfer agents in good yields and in high chemo-, regio-, and stereoselectivity without formation of decarboxylated byproducts. Reaction monitoring via ESI-MS was used to support the formation of chelated Pd species through the catalytic cycle. Additionally, some Heck adducts were successfully used in the total synthesis of pharmacologically active γ-lactones. 16 5180-3