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 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Trapping enols of esters and lactones with diazomethane
Synthesis of Indolylindolines Mediated by tert-BuNH2
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
One-potsynthesis of conformationallyrestrictedspirooxindoles
Role of lipid peroxidation in biliary obstruction in the rat