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).
Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase
Transesterifications mediated by t-BuNH2
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Trapping enols of esters and lactones with diazomethane
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
One-potsynthesis of conformationallyrestrictedspirooxindoles