1309774-76-2Relevant academic research and scientific papers
Chiral calix[4]arenes bearing amino alcohol functionality as membrane carriers for transport of chiral amino acid methylesters and mandelic acid
Bozkurt, Selahattin,Yilmaz, Mustafa,Sirit, Abdulkadir
scheme or table, p. 129 - 136 (2012/03/27)
Novel chiral calix[4]arene derivatives bearing amino alcohol moieties at the lower rim have been synthesized from the reaction of p-tert-butylcalix[4] arene diester with various amino alcohols. The transport of amino acid esters (phenylglycine, phenylalanine, and tryptophan methyl esters hydrochloride) and mandelic acid were studied through chloroform bulk liquid membrane system using chiral calix[4]arenes 15-20. All these receptors have been found to act as carriers for transport of aromatic amino acid methylesters and mandelic acid from the aqueous source phase to the aqueous receiving phase. The influence of calixarene and guest structures upon transport through liquid membrane is discussed.
Amino alcohol based chiral solvating agents: Synthesis and applications in the NMR enantiodiscrimination of carboxylic acids
Bozkurt, Selahattin,Durmaz, Mustafa,Naziroglu, Hayriye Nevin,Yilmaz, Mustafa,Sirit, Abdulkadir
experimental part, p. 541 - 549 (2011/06/19)
Four optically active amino alcohols were synthesized via the ring opening of (R)-N-(2,3-epoxypropyl)phthalimide with (R)-2-phenyl glycinol, (1R,2S)-cis-1-amino-2-indanol, (R)-2-amino-1-butanol and (S)-phenyl ethylamine in 73-93% yields. The enantioselect
