2007
Trapping enols of esters and lactones with diazomethane.Martha S. Morales-Ríos, Perla Y. López-Camacho, Oscar R. Suárez-Castillo, Pedro Joseph-Nathan. DOI: http://dx.doi.org/10.1016/j.tetlet.2007.02.006
Abstract
A series of regioisomeric ketene-O,O-dialkyl acetals were prepared from ambident ?-dicarbonylfuroindoles by trapping the enol tautomers of esters and lactones with diazomethane. Definitive structural characterization was accomplished by X-ray crystal structure determination on a ketene-O,O-dimethyl acetal (R = Me).
Synthesis of Acetamido(indole-3-yl)propanol Derivatives
One-potsynthesis of conformationallyrestrictedspirooxindoles
Trapping enols of esters and lactones with diazomethane
Role of lipid peroxidation in biliary obstruction in the rat.
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Synthesis of Indolylindolines Mediated by tert-BuNH2
Transesterifications mediated by t-BuNH2
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor