Producción Científica Profesorado

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.



Producto de Investigación




Artículos relacionados

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

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

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

Unimolecular rearrangements of ketene-O,O-acetals and fragmentations occurring in the gas phase

The absoluteconfiguration of cuauhtemone and related compounds

First Total Synthesis of ()-Flustraminol B

Stereochemical assignment of naturally occurring 2,3-epoxy-2-methylbutanoate esters

One-potsynthesis of conformationallyrestrictedspirooxindoles

13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters

Trapping enols of esters and lactones with diazomethane