Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI2–Et3N–H2O†
Tobias Ankner,Anna Said Stålsmeden,Göran Hilmersson
Chemical Communications Pub Date : 06/06/2013 00:00:00 , DOI:10.1039/C3CC41642A
Abstract

A novel electron poor protection group for amines has been developed. It undergoes rapid cleavage by SmI2–Et3N–H2O and its orthogonality towards the regular benzyl carbamate group (CBz) under reductive or transfer hydrogenolytic conditions is reported.

Graphical abstract: Selective cleavage of 3,5-bis-(trifluoromethyl)benzylcarbamate by SmI2–Et3N–H2O