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).
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
The absoluteconfiguration of cuauhtemone and related compounds
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Synthesis of Acetamido(indol-3-yl)propanol Derivatives
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase