Scientific Production Faculty

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.



Research Product




Related articles

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

Reactivity of TpMe2Ir(C2H4)(DMAD) with carboxylic acids. A DFT study on geometrical isomers and stru...

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

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

Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea

Synthesis of 6-bromo-2-arylindoles using 2-iodobenzoic acid as precursor

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

One-potsynthesis of conformationallyrestrictedspirooxindoles

Role of lipid peroxidation in biliary obstruction in the rat.

Firsttotalsyntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Fl...