439916-91-3

Upstream product

• 96-35-5 glycolic acid methyl ester 
• 439916-77-5 [(S)-1-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylcarbamoyl)-2-methyl-propyl]-carbamic acid benzyl ester 
• 2443-71-2 benzyl (S)-(1-hydrazineyl-3-methyl-1-oxobutan-2-yl)carbamate 
• 85-44-9 phthalic anhydride 

Downstream Products

• 439917-01-8 C₂₆H₃₉N₃O₉ 

Relevant academic research and scientific papers

Oligomerization of N-aminodipeptides: to the synthesis of heterogeneous backbone with 1:1 α:α-N-amino aminoacid residue patterns

A large number of N-aminodipeptides compounds have been obtained via a Mitsunobu protocol performed in solution or by solid-phase synthesis. The oligomerization of some of them has been studied in solution or on solid support leading to the formation of 1:1[α:α-N-amino]mers.

Original and efficient method for the preparation of N-aminoamide pseudodipeptides in high optical purity

N-Aminoamide pseudodipeptides ZAAΨ[CO-N(NPht)]-AAOR can be easily obtained via the Mitsunobu protocol by using α-hydroxyesters as alcohol partners and aminoacid phthaloyl hydrazide derivatives as acidic partners. The direct conversion of the phthaloyl group into tert-butyloxycarbonyl can be performed in a three-stage one-pot protocol.