83597-39-1

Upstream product

• 110-99-6 2,2'-oxybis-acetic acid 
• 3081-24-1 H-Phe-OEt 
• 3182-93-2 (L)-phenylalanine ethyl ester hydrochloride 
• 21062-20-4 diglycolyl chloride 

Downstream Products

• 114935-99-8 (3S,11S,15S,18S,26S,29S)-3,11-Dibenzyl-15,18,26,29-tetrakis-benzyloxymethyl-1,7,13,22-tetraoxa-4,10,16,19,25,28-hexaaza-cyclotriacontan-5,9,14,17,20,24,27,30-octaone 
• 114950-71-9 N-[(S)-1-(2-Hydroxy-ethoxymethyl)-2-phenyl-ethyl]-2-[((S)-1-hydroxymethyl-2-phenyl-ethylcarbamoyl)-methoxy]-acetamide 
• 103256-26-4 (S)-2-[(S)-2-(2-{[(S)-1-((S)-1-Carboxy-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methoxy}-acetylamino)-3-phenyl-propionylamino]-3-phenyl-propionic acid 
• 103256-24-2 (S)-2-[(S)-2-(2-{[(S)-1-((S)-1-Ethoxycarbonyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-methoxy}-acetylamino)-3-phenyl-propionylamino]-3-phenyl-propionic acid ethyl ester 
• 114935-97-6 (3S,11S,15S,18S,26S,29S)-3,11-Dibenzyl-15,18,26,29-tetraisobutyl-1,7,13,22-tetraoxa-4,10,16,19,25,28-hexaaza-cyclotriacontan-5,9,14,17,20,24,27,30-octaone 
• 114935-98-7 C₅₀H₇₆N₆O₁₃ 
• 103256-28-6 (3S,11S,15S,18S,26S,29S)-15,18,26,29-Tetrabenzyl-3,11-diisobutyl-1,7,13,22-tetraoxa-4,10,16,19,25,28-hexaaza-cyclotriacontan-5,9,14,17,20,24,27,30-octaone 
• 80757-20-6 (S,S)-9,17-dibenzyl-1,4,7,13-tetraoxa-10,16-diazacyclo-octadecane-11,15-dione 
• 83597-45-9 (3S,11S,15S,23S)-3,11,15,23-Tetrabenzyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosane-2,5,9,12,17,21-hexaone 
• 83597-43-7 N,N'-3-oxa-pentanoyl-(S,S)-diphenylalanine 
• 83597-41-5 N,N'-bis[(1S)-1-benzyl-2-hydroxyethyl]diglycolyldiamide 

Relevant academic research and scientific papers

SYNTHESES OF MACROCYCLES FROM L-AMINO ACID AND THEIR SELECTIVE TRANSPORT OF AMINO ESTERS SALTS THROUGH AN ORGANIC LIQUID MEMBRANE

Syntheses of 18-membered macrocycle 17, 24-membered macrocycles 18, 19, and 30-membered macrocycles 20, 21, 22, 23, 25, were achieved by using diglycolic acid and amino acids as constituents.Selective transport of amino ester salts through an organic liqu

CHIRAL AMINOACID CONTAINING ACYCLIC LIGANDS-I. SYNTHESES AND CONFORMATIONS

Synthesis and spectral properties of optically active acyclic ligands, containing two (S)-phenylalanine residues (3a-f) are described.The synthesis is achieved by two different routes.Conformational studies in different solvents are performed by dilution and temperature-dependent experiments of 1H and 13C NMR spectroscopy.

SYNTHESES OF MACROCYCLES FROM L-AMINO ACID

Syntheses of 24-membered macrocycles were achieved by using L-phenyl-alanine and L-leucine as constituets.