16748-79-1

Upstream product

• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 96157-57-2 bis(pentafluorophenyl)sulfite 
• 771-61-9 2,3,4,5,6-pentafluorophenol 

Downstream Products

• 24715-22-8 N-benzyloxycarbonylglycine β-dimethylaminoethyl ester 
• 33912-87-7 N-benzyloxycarbonylglycyl-L-valine (Z-Gly-Val) 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 79990-06-0 ZGlyNEt₂ 
• 1049736-72-2 4(N),10(N)-bis-[N-(benzyloxycarbonyl)glycyl]-1,7-dimethyl-1,4,7,10-tetraazacyclododecane 
• 29637-79-4 N-Benzyloxycarbonylglycine β-dimethylaminoethyl ester methiodide 
• 138540-56-4 C₆₀H₈₉N₉O₂₀ 

Relevant academic research and scientific papers

SN2'-Reactions of Peptide Aziridines. A Cuprate-Based Approach to (E)-Alkene Isosteres

Alkenylaziridines were prepared from allylic alcohols via Sharpless epoxidation, oxirane to aziridine conversion under modified Staudinger conditions, and Wittig chain extension.Alternatively, β-hydroxy α-amino acids such as threonine can serve as readily

Bis(pentaluorophenyl) sulfite - A new reagent for the synthesis of activated pentafluorophenyl esters of N-protected amino acids

A method was proposed for the preparation of bis(perfluorophenyl) sulfite, an effective new reagent for the synthesis of pentafluorophenyl esters of N-protected amino acids without racemization.