Producción Científica Profesorado

Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2



Suárez Castillo, Oscar Rodolfo

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.



Producto de Investigación




Artículos relacionados

Synthesis of Indolylindolines Mediated by tert-BuNH2

Cascade [1,3]-Sigmatropic Rearrangements of Ketene O,O-Acetals: Kinetic and DFT Level Mechanistic St...

Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters

Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles

Role of lipid peroxidation in biliary obstruction in the rat

Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives

Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling

Synthesis of Acetamido(indol-3-yl)propanol Derivatives

Conformationalstudies of N-carbomethoxy-2-alkoxyindolenines by dynamic NMR, crystallography, and mol...

Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase