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
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles
The absoluteconfiguration of cuauhtemone and related compounds
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Synthesis of Acetamido(indol-3-yl)propanol Derivatives
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea