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 Bromoindole Alkaloids from Laurencia brongniartii
Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase
Trapping enols of esters and lactones with diazomethane
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
One-potsynthesis of conformationallyrestrictedspirooxindoles
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Role of lipid peroxidation in biliary obstruction in the rat