188051-31-2

Upstream product

• 873-75-6 4-bromobenzenemethanol 
• 767-00-0 4-cyanophenol 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 169267-67-8 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid 
• 169267-65-6 1-Bromo-8-tert-butoxycarbonylamino-7-oxo-3-oxa-6-aza-1(1,4),4(1,4)-dibenzaoctaphane 
• 155720-37-9 11-Bromo-5-amino-3-oxa-1(1,4),4(1,4)-dibenzapentaphane 
• 155720-38-0 11-Bromo-4-cyano-3-oxa-1(1,4),4(1,4)-dibenzatetraphane 
• 141-86-6 2.6-diaminopyridine 
• 188051-24-3 (4S)-Prop-2-enyl-4-benzyl-3,6-dioxo-11-amino-12,2,5-diaza-1(1,3)-benzanonaphane-9-carboxylate 
• 188051-29-8 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid fluoride 
• 220891-73-6 (S)-2-Amino-N-(6-amino-pyridin-2-yl)-3-phenyl-propionamide 
• 188051-21-0 (4S)-4-tert-Butoxycarbonyl-4-benzyl-3-oxo-11,4-diamino-12,2-diaza-1(1,3)-benzatetraphane 

Relevant academic research and scientific papers

Synthesis and binding properties of a macrocyclic peptide receptor

Macrocyclic receptor 1 has been synthesised, as a racemate and as a single enantiomer, utilising a Stille coupling for the formation of the biphenyl portion and a macrolactamisation as the final step. The binding properties for the racemic and the homochi

Modified synthesis and binding properties of a peptide receptor

Macrocyclic receptor 9, has been prepared in homochiral form. The receptor shows selectivity for certain dipeptides, and most notably a strong preference for N-Cbz-β-alanyl amino acids over N-Cbz-β-alanyl lactic acids.