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).
The absoluteconfiguration of cuauhtemone and related compounds
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters
Synthesis of Indolylindolines Mediated by tert-BuNH2
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles
First Total Synthesis of ()-Flustraminol B
Trapping enols of esters and lactones with diazomethane
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives