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

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

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

Photochemical rearrangements of highly functionalized longipinene derivatives

DFT and NMR parameterized conformation of valeranone

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

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

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

First Total Synthesis of ()-Flustraminol B

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

Synthesis of Indolylindolines Mediated by tert-BuNH2