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.
DFT and NMR parameterized conformation of valeranone
Synthesis of Indolylindolines Mediated by tert-BuNH2
Cleavage of alkoxycarbonylprotectinggroups from carbamates by t-BuNH2
Mechanisticstudies of the photochemicalrearrangement of 1-oxolongipin-2-ene derivatives
Regioselective Synthesis of 3-Indolyl(alkoxy)acetates
Synthesis of Bromoindole Alkaloids from Laurencia brongniartii
Photochemical rearrangements of highly functionalized longipinene derivatives