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).
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Synthesis of Acetamido(indol-3-yl)propanol Derivatives
Transesterifications mediated by t-BuNH2
One-potsynthesis of conformationallyrestrictedspirooxindoles