96308-17-7

Upstream product

• 42538-64-7 Boc-glycine cesium salt 
• 100-39-0 benzyl bromide 
• 89004-82-0 potassium bis(tert-butoxycarbonyl)amide 
• 5437-45-6 Benzyl bromoacetate 
• 51779-32-9 iminodicarboxylic acid di-tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 54244-69-8 tert-butoxycarbonylamino-acetic acid benzyl ester 

Downstream Products

• 132090-36-9 Boc₂-Gly-Gly-Phe-Leu-OBzl 
• 132090-35-8 Boc₂-Gly-Phe-Leu-OBzl 
• 132090-27-8 Boc₂-Gly-ONp 
• 113568-27-7 C₂₈H₃₅N₃O₉ 
• 113568-26-6 C₂₈H₃₆N₂O₇ 

Relevant academic research and scientific papers

A Convenient One-Flask Preparation of Di-t-butyl Iminodicarbonate: A Versatile Gabriel Reagent

An improved synthesis of di-t-butyl iminodicarbonate from formamide and di-t-butyl dicarbonate with dimethylaminopyridine as a catalyst followed by aminolytic removal of the formyl group is described as well as a few applications related to the synthesis of primary amines.

Preparation and Properties of Nα-Di-tert-Butoxycarbonyl Amino Acids. Applicability in the Synthesis of Leu-Enkephalin

The synthesis of Nα-di-tert-butoxycarbonyl amino acids starting from the corresponding mono-derivatives via a three-step route is reported.The latter were converted into a suitable ester and then exhaustively t-butoxycarbonylated, after which t