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.
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
The absoluteconfiguration of cuauhtemone and related compounds
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Trapping enols of esters and lactones with diazomethane
Role of lipid peroxidation in biliary obstruction in the rat
One-potsynthesis of conformationallyrestrictedspirooxindoles