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.
Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea
Trapping enols of esters and lactones with diazomethane
Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling
Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine
Transesterifications mediated by t-BuNH2
Synthesis of Indolylindolines Mediated by tert-BuNH2
One-potsynthesis of conformationallyrestrictedspirooxindoles
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Configuration, stereodynamics and crystal structure of 3-substituted-2-oxofuro[2,3-b]indoles