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).
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Trapping enols of esters and lactones with diazomethane
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Transesterifications mediated by t-BuNH2
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Synthesis of Indolylindolines Mediated by tert-BuNH2
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling