139449-11-9

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 70853-26-8 N-carbobenzoxy-L-leucinal 
• 7517-19-3 methyl (L)-leucinate hydrochloride 

Relevant academic research and scientific papers

Studies on the Synthesis of Cyanomethyleneamino Pseudopeptides

Various cyanomethyleneamino pseudodipeptides were easily prepared in high yield by the Lewis acid catalyzed addition of trimethylsilyl cyanide to unstable aldimine intermediates, obtained from the reaction of N-protected α-amino aldehydes with C-protected

Synthesis of Ψ[CH(CN)NH] pseudopeptides. A new peptide bond surrogate

An easy and versatile general method for the preparation of the new peptide bond surrogate Ψ[CH (CN)NH], by the Lewis acid catalyzed reaction of N-protected α-amino aldehydes with a C-protected amino acid or peptide in the presence of TMSCN, is described.