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).
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
One-potsynthesis of conformationallyrestrictedspirooxindoles
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Trapping enols of esters and lactones with diazomethane
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives