76413-56-4

Upstream product

• 134469-06-0 thiazolidine-2-thione 
• 1142-20-7 N-Cbz-Ala 

Downstream Products

• 17460-58-1 (2S)-2-[((2S)-2-{[(benzyloxy)carbonyl]amino}propanoyl)amino]-3-hydroxypropanoic acid 
• 3235-14-1 (S)-2-((S)-2-Benzyloxycarbonylamino-propionylamino)-3-phenyl-propionic acid methyl ester 
• 2503-31-3 N-benzyloxycarbonyl-L-alanylglycine 
• 2503-32-4 ethyl N-(benzyloxycarbonyl)-L-alanylglycinate 
• 13585-98-3 N^α-benzyloxycarbobyl-L-alanyl-L-alanyl-L-alanine 
• 136206-25-2 17β-(N-benzyloxycarbonyl-L-alanyl)hydrazonoestra-1,3,5(10)-trien-3-ol 
• 136206-17-2 17β-(N-benzyloxycarbonyl-L-alanyl)aminoestra-1,3,5(10)-trien-3-ol 
• 16305-78-5 Cbz-L-ala-L-gly-Cbz 
• 2768-53-8 N-benzyloxycarbonyl-L-alanyl-L-phenylalanine 
• 16012-70-7 benzyloxycarbonyl-L-alanyl-L-alanine 

Relevant academic research and scientific papers

Peptide-bond Formation, Chemoselective Acylation of Amino Acids, and Crosslinking Reaction between Amino Acids Utilizing a Functional Five-membered Heterocycle, 1,3-Thiazolidine-2-thione

The monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thiones has been extended to the peptide-bond formation, the chemoselective acylation of amino acids having multifunctional groups, and the crosslinking reaction between amino acids.

MONITORED AMINOLYSIS OF 3-ACYL-1,3-THIAZOLIDINE-2-THIONE WITH AMINO ACID AND ITS DERIVATIVE: PEPTIDE BOND FORMATION, CHEMOSELECTIVE ACYLATION, AND BRIDGING REACTION

As a new extention of the monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thione, its applications to peptide bond formation, chemoselective acylation of amino acid, and bridging reaction on the enzyme model are reported.

Studies on Peptides. XCIV. Thiazoline-2-thione as a Carboxyl-activating Reagent for Peptide Synthesis

3-Acyl derivatives obtained from the DCC condensation of Nα-protected amino acids and thiazoline-2-thione were found to be useful for peptide synthesis, in the same way as active esters.Keywords---3-acylthiazoline-2-thione derivatives of N