Literature DB >> 18491864

Chiral selector with multiple hydrogen-bonding sites in a macrocyclic cavity.

Tadashi Ema1, Daisuke Tanida, Kyoko Sugita, Takashi Sakai, Ken-ichiro Miyazawa, Atsushi Ohnishi.   

Abstract

Chiral macrocycles with the hydrogen bond donor/acceptor sites in the cavity were synthesized and covalently bonded to silica gel to give chiral stationary phases (CSPs), which showed excellent abilities to resolve various chiral compounds, such as benzoin and Co(acac)3, in HPLC. Various organic solvents could be used as the mobile phase to optimize the resolution efficiency of CSPs, and in some cases, even MeCN, MeOH, and CO(2) could be used for the complete resolution of enantiomers.

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Year:  2008        PMID: 18491864     DOI: 10.1021/ol800940j

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Chiral discrimination of α-hydroxy acids and N-Ts-α-amino acids induced by tetraaza macrocyclic chiral solvating agents by using 1H NMR spectroscopy.

Authors:  Caixia Lv; Lei Feng; Hongmei Zhao; Guo Wang; Pericles Stavropoulos; Lin Ai
Journal:  Org Biomol Chem       Date:  2017-01-27       Impact factor: 3.876

2.  Determination of enantiomeric excess of carboxylates by fluorescent macrocyclic sensors.

Authors:  Ali Akdeniz; Tsuyoshi Minami; Sagiri Watanabe; Maki Yokoyama; Tadashi Ema; Pavel Anzenbacher
Journal:  Chem Sci       Date:  2015-12-14       Impact factor: 9.825

  2 in total

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