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
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles
Synthesis of Indolylindolines Mediated by tert-BuNH2
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
The absoluteconfiguration of cuauhtemone and related compounds
Trapping enols of esters and lactones with diazomethane
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters