56538-74-0

Upstream product

• 128254-55-7 N-benzoyl-2-ethylthioglycine methyl ester 
• 21286-78-2 methyl N-benzoyl-2-methoxyglycinate 
• 55-21-0 benzamide 
• 19791-95-8 α-hydroxyhippuric acid 
• 56538-63-7 1-benzoylamino-1-(methylthio)acetic acid 
• 56538-67-1 N-benzoyl-2-methylthioglycine methyl ester 

Downstream Products

• 120341-28-8 Methyl 2-(N-Benzoylamino)-2-(dimethoxyphosphinyl)ethanoate 
• 290346-20-2 (Z)-2,3-bis(N,N'-benzoylamino)maleic acid dimethyl ester 

Relevant academic research and scientific papers

Conotoxin analogues and methods for synthesis of intramolecular dicarba bridge-containing peptides

According to the present invention, there is provided a range of new conotoxin derivatives and methods for synthesizing these analogues and other intramolecular dicarba bridge-containing peptides, including dicarba-disulfide bridge-containing peptides.

Stereocontrolled backbone connection of peptides by C = C-double bonds

Treatment of peptides containing an α-chloroglycine residue with triethylamine and catalytic amounts of triphenylphosphine constitutes an efficient method for the stereoselective synthesis of amino acid and peptide dimers bridged by a C = C-double bond. The dimers can be converted into novel peptide structures by standard methods of peptide synthesis. (C) 2000 Elsevier Science Ltd.