1966
Synthesis of acetamido(indole-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(indole-3-yl)propanol derivatives (5-7) have been synthesized using a variety of reductive reactions performed on the corresponding O-methyl oximes of an indole-3-yl ester and of several indole-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.
One-potsynthesis of conformationallyrestrictedspirooxindoles
Trapping enols of esters and lactones with diazomethane
The absoluteconfiguration of cuauhtemone and related compounds
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
First Total Synthesis of ()-Flustraminol B
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters