133565-25-0

Upstream product

• 63-91-2 L-phenylalanine 
• 2052-49-5 tetra(n-butyl)ammonium hydroxide 

Downstream Products

• 84293-32-3 (S)-2-[2-(2-{2-[((S)-1-Carboxy-2-phenyl-ethylcarbamoyl)-methoxy]-ethoxy}-ethoxy)-acetylamino]-3-phenyl-propionic acid 
• 84308-23-6 N,N'-3-thia-pentanoyl-(S,S)-diphenylalanine 
• 583-47-1 4-benzyl-oxazolidine-2,5-dione 
• 84293-33-4 (S)-2-{2-[2-(2-{2-[((S)-1-Carboxy-2-phenyl-ethylcarbamoyl)-methoxy]-ethoxy}-ethoxy)-ethoxy]-acetylamino}-3-phenyl-propionic acid 
• 84293-31-2 (S)-2-(2-{2-[((S)-1-Carboxy-2-phenyl-ethylcarbamoyl)-methoxy]-ethoxy}-acetylamino)-3-phenyl-propionic acid 
• 84308-22-5 N,N'-pentanoyl-(S,S)-diphenylalanine 

Relevant academic research and scientific papers

Chiral discrimination of α-amino acids with a C2-symmetric homoditopic receptor

Chiral discrimination of α-amino acids has been realized by a C 2-symmetric homoditopic receptor, which is based on a binaphthyl chiral skeleton with 2,2′diisopropoxy substituents and a common binding side arm, (o-carboxamido)-trifluoroacetophe

Enantioselective molecular recognition of chiral organic ammonium ions and amino acids using cavitand-salen-based receptors

Two new receptors, a cavitand-salen (2) and a uranyl-cavitand-salen (3), for the selective molecular recognition of chiral ammonium ion pairs, where the amino acid is the countercation or counteranion of the ion pair, were designed and synthesized. UV/Vis

Heteroditopic chiral uranyl-salen receptor for molecular recognition of amino acid ammonium salts

A new heteroditopic chiral uranyl-salen complex incorporating two pyrenyl groups was designed and synthesized for the recognition of ammonium salts, tetrabutylammonium (TBA) and tetramethylammonium (TMA) amino acids. UV/Vis measurements indicate the formation of 1:1 host-guest complexes with high association constants and an excellent en-antiomeric discrimination between the two enantiomers of phenylalanine-TMA. T-ROESY NMR experiments confirm cation-π and CH-π interactions between the TBA and TMA cations and the two pyrenyl arms, leading to the strong stability of the complexes. This is the first report of a uranyl receptor able to recognize chiral carboxylate guests.

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.