1429753-18-3

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 103-82-2 phenylacetic acid 
• 87976-65-6 (S)-tert-butyl (1-((2-hydroxyethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate 
• 844697-83-2 (2-phenyl)-selenoacetic acid 

Downstream Products

• 1429753-17-2 (S)-2-(2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)ethaneseleninic acid 
• 1429753-20-7 (S)-Se-(2-(2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)ethyl) 4-methylbenzenesulfonoselenoate 
• 1429753-23-0 (6S,14R,19S)-19-amino-6-benzyl-14-((carboxymethyl)carbamoyl)-2,2-dimethyl-4,7,16-trioxo-3-oxa-12-thia-11-selena-5,8,15-triazaicosan-20-oic acid 

Relevant academic research and scientific papers

Biohybrid-Se-S-coupling reactions of an amino acid derived seleninate

We describe the synthesis of the N-(2-seleninatoethyl) amide of N-Bocphenylalanine, serving here as a peptide model, and its reductive coupling reactions under mild conditions with unprotected thiouridine and glutathione. Selenosulfide products such as these comprise reversibly conjugated bio-components, and can potentially find uses as probes of biological function, such as enzyme inhibitors, delivery systems, or structural mimics.