439916-77-5

Upstream product

• 85-44-9 phthalic anhydride 
• 2443-71-2 benzyl (S)-(1-hydrazineyl-3-methyl-1-oxobutan-2-yl)carbamate 
• 501-53-1 benzyl chloroformate 
• 24210-19-3 methyl (2S)-3-methyl-[(benzyloxy)carbonylamino]butanoate 
• 4070-48-8 L-Valine methyl ester 

Downstream Products

• 439916-91-3 [((S)-2-Benzyloxycarbonylamino-3-methyl-butyryl)-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-amino]-acetic acid methyl ester 
• 439917-01-8 C₂₆H₃₉N₃O₉ 

Relevant academic research and scientific papers

A family of strong low-molecular-weight organogelators based on aminoacid derivatives

A new family of potent aminoacid-type organogelators obtained via an easy and unexpensive way is described. We demonstrated that structural variations onto the side chains of the aminoacid derivatives allowed modulations of the gelation properties. The or

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.