2007
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2. Oscar R. Suárez-Castillo, Luis Alberto Montiel-Ortega, Myriam Meléndez-Rodríguez, Maricruz Sánchez-Zavala. DOI: http://dx.doi.org/10.1016/j.tetlet.2006.11.024
Abstract
An efficient, simple protocol for the selective cleavage of a variety of N-alkoxycarbonyl protecting groups by t-BuNH2/MeOH is described. The scope of the procedure was explored for a series of indole, aniline and pyrrolidine carbamate derivatives containing other potentially reactive functional groups affording a clean cleavage of the carbamate group.
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters
Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2
Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor
Trapping enols of esters and lactones with diazomethane
Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters