Producción Científica Profesorado

Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2



Sánchez Zavala, Maricruz

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


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.






Artículos relacionados

Synthesis of Indolylindolines Mediated by tert-BuNH2

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

Mechanisticstudies of the photochemicalrearrangement of 1-oxolongipin-2-ene derivatives

Regioselective Synthesis of 3-Indolyl(alkoxy)acetates

Conformationalstudies of N-carbomethoxy-2-alkoxyindolenines by dynamicNMR, crystallography, and mole...

Quirogane, Prenopsane, and Patzcuarane Skeletons Obtained by Photochemically Induced Molecular Rearr...

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

First Total Synthesis of ()-Flustraminol B

DFT and NMR parameterized conformation of valeranone

Preparation of 3-hydroxyoxindoles with dimethyldioxirane and their use for the synthesis of naturalp...