1025554-41-9Relevant academic research and scientific papers
A mild and efficient chemoselective: N-benzyloxycarbonylation of amines using TBAB a catalyst under solvent-free conditions
Babu, Kothamasu Suresh,Rao, Vidadala Rama Subba,Rao, Ravu Ranga,Babu, Sakhamuri Sivaram,Rao, Janaswami Madhusudana
, p. 393 - 396 (2009)
We describe a mild and efficient method for the chemoselective N-benzyloxycarbonylation of amines by treatment amines and aminoesters with benzyloxycarbonyl chloride (Cbz-Cl) in the presence of TBAB under solvent-free in excellent yields. The method is ge
N-Benzyloxycarbonylation of amines in the ionic liquid [TPA][l-Pro] as an efficient reaction medium
Suryakiran,Chinni Mahesh,Ramesh,Jon Paul Selvam,Venkateswarlu
, p. 2607 - 2610 (2008)
An efficient method for the N-benzyloxycarbonylation of amines is described. The reaction of amines with Cbz-Cl in the ionic liquid [TPA][l-Pro] afforded the corresponding N-Cbz derivatives in excellent yields. The method is versatile for the preparation
Insertion of benzene rings into the amide bond: one-step synthesis of acridines and acridones from aryl amides
Pintori, Didier G.,Greaney, Michael F.
supporting information; experimental part, p. 168 - 171 (2010/03/30)
"Chemical Equation Presented" Insertion of benzene rings into the amide bond using the reactive intermediate benzyne is described. Aromatic amides undergo smooth insertion when treated with O-triflatophenyl silane benzyne precursors, producing versatile a
