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To enzyme analogues by lock and key chemistry with crown compounds. Part 1. Enantiomeric differentiation by configurationally chiral cryptands synthesised from L-tartaric acid and D-mannitol.

作者信息

Curtis W D, Laidler D A, Stoddart J F, Jones G H

出版信息

J Chem Soc Perkin 1. 1977 Aug;15:1756-69. doi: 10.1039/p19770001756.

DOI:10.1039/p19770001756
PMID:561110
Abstract
摘要

相似文献

1
To enzyme analogues by lock and key chemistry with crown compounds. Part 1. Enantiomeric differentiation by configurationally chiral cryptands synthesised from L-tartaric acid and D-mannitol.
J Chem Soc Perkin 1. 1977 Aug;15:1756-69. doi: 10.1039/p19770001756.
2
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Enantiomeric separations of amino alcohols by packed-column SFC on Hypercarb with L-(+)-tartaric acid as chiral selector.以L-(+)-酒石酸为手性选择剂,在Hypercarb填充柱上通过超临界流体色谱法对氨基醇进行对映体分离。
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Simultaneous determination of anions and cations by ion-exclusion chromatography-cation-exchange chromatography with tartaric acid/18-crown-6 as eluent.以酒石酸/18-冠-6为洗脱剂,采用离子排斥色谱-阳离子交换色谱法同时测定阴离子和阳离子。
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7
Cesium cation templated selective synthesis of a "cone-shaped" sugar macrotricyclic cryptand: A dual anion-cation molecular recognition of potassium tartrate.铯阳离子模板法选择性合成“锥形”糖基大环穴醚:酒石酸钾的双阴阳离子分子识别
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Molecular recognition properties of tartrates and metal-tartrates in solution and gas phase.酒石酸盐及金属酒石酸盐在溶液和气相中的分子识别特性。
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Direct chiral resolution of tartaric acid in food products by ligand exchange capillary electrophoresis using copper(II)-D-quinic acid as a chiral selector.
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Formation of chiral surface with enantiomeric tartaric acid on gemini-structured self-assembled monolayers.在双子结构自组装单分子层上用对映体酒石酸形成手性表面。
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