Synthesis of Acetamido(indol-3-yl)propanol Derivatives
Suárez Castillo, Oscar Rodolfo
1966
Synthesis of acetamido(indol-3-yl)propanol derivatives. Morales-Ríos M. S., Zepeda L. G., Suárez-Castillo O. R., Joseph-Nathan P. DOI: 10.3987/COM-96-7474
Abstract
A series of acetamido(indol-3-yl)propanol derivatives (5-7) has been synthesized using a variety of reductive reactions performed on the corresponding O-methyl oximes of an indol-3-yl ester and of several indol-3-yl alcohol derivatives. The O-methyl oximes were prepared in good yields by acylation of the corresponding zinc salt of indole, followed by O-methyl oximation.
Artículos relacionados
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles
First Total Synthesis of ()-Flustraminol B
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Synthesis of Indolylindolines Mediated by tert-BuNH2
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii