74761-86-7

Upstream product

• 74761-83-4 2-((E)-2-Benzenesulfonyl-vinyl)-2,6-bis-benzoylamino-hexanoic acid methyl ester 
• 98-88-4 benzoyl chloride 
• 67565-17-7 4-(4-benzoylamino-butyl)-2-phenyl-4H-oxazol-5-one 
• 74761-81-2 N-{4-[4-((E)-2-Benzenesulfonyl-vinyl)-5-oxo-2-phenyl-4,5-dihydro-oxazol-4-yl]-butyl}-benzamide 
• 116783-33-6 N^α-Benzoyllysine 
• 152774-39-5 Methyl N^α,N^ε-dibenzoyl-2-<2'-(phenylseleno)ethyl>lysinate 

Downstream Products

• 74761-90-3 2,6-Bis-benzoylamino-2-vinyl-hexanoic acid 
• 714222-57-8 (+/-)-α,β-dimethyl N-benzoyl-α-formylaspartate 
• 714222-56-7 (+/-)-methyl N^α,N^ε-dibenzoyl-α-formyllysinate 
• 86555-45-5 rac-dimethyl 2-benzamidosuccinate 
• 133787-17-4 α,ε-N,N'-dibenzoyllysine methyl ester 
• 714222-63-6 (+/-)-α,β-dimethyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinylaspartate 
• 714222-62-5 (+/-)-methyl N^α,N^ε-dibenzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyllysinate 

Relevant academic research and scientific papers

Formal α-Vinylation of Amino Acids. Use of a New Benzeneselenolate Equivalent

A new synthetic approach to the formal α-vinylation of α-amino acids is described, in which the readily available electrophile, ethylene oxide, serves as the vinyl cation equivalent.N-Benzoyl α-amino esters bearing appropriate side-chain protecting groups