The application of quasi-enantiomeric trianglamine macrocycles as chiral probes for anion recognition in ion trap ESI mass spectrometry
This paper reports the synthesis and application of quasi-enantiomeric trianglamine macrocycles for chiral analysis using ion trap ESI mass spectrometry. The quasi-enantiomeric macrocycles were shown to display chiroselection towards a series of enantiomerically pure carboxylic acids and therefore a...
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| Published in | Tetrahedron: asymmetry Vol. 18; no. 14; pp. 1648 - 1654 |
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| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
OXFORD
Elsevier Ltd
30.07.2007
Elsevier |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0957-4166 1362-511X |
| DOI | 10.1016/j.tetasy.2007.07.011 |
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| Abstract | This paper reports the synthesis and application of quasi-enantiomeric trianglamine macrocycles for chiral analysis using ion trap ESI mass spectrometry. The quasi-enantiomeric macrocycles were shown to display chiroselection towards a series of enantiomerically pure carboxylic acids and therefore act as chiral probes for anions in the gas phase and in solution. |
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| AbstractList | This paper reports the synthesis and application of quasi-enantiomeric trianglamine macrocycles for chiral analysis using ion trap ESI mass spectrometry. The quasi-enantiomeric macrocycles were shown to display chiroselection towards a series of enantiomerically pure carboxylic acids and therefore act as chiral probes for anions in the gas phase and in solution. (c) 2007 Elsevier Ltd. All rights reserved. This paper reports the synthesis and application of quasi-enantiomeric trianglamine macrocycles for chiral analysis using ion trap ESI mass spectrometry. The quasi-enantiomeric macrocycles were shown to display chiroselection towards a series of enantiomerically pure carboxylic acids and therefore act as chiral probes for anions in the gas phase and in solution. |
| Author | Kuhnert, Nikolai Marsh, David Nicolau, Daniel C. |
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| CitedBy_id | crossref_primary_10_1016_j_aca_2017_03_021 crossref_primary_10_1002_cjoc_200990009 crossref_primary_10_1039_c2ob25171j crossref_primary_10_1016_j_tetlet_2013_05_085 crossref_primary_10_1002_adsc_200800801 crossref_primary_10_1021_acs_joc_6b02868 crossref_primary_10_1007_s10593_012_1080_5 crossref_primary_10_1016_j_tetlet_2018_08_059 crossref_primary_10_1002_chem_202101510 crossref_primary_10_1007_s11224_008_9373_0 crossref_primary_10_1039_c0ob00944j crossref_primary_10_1002_rcm_3344 crossref_primary_10_1002_rcm_6203 crossref_primary_10_1002_rcm_6401 crossref_primary_10_1016_j_tet_2013_11_002 crossref_primary_10_1039_C6RA06095A crossref_primary_10_1021_ja310620c crossref_primary_10_1002_jms_1326 crossref_primary_10_1039_c004873a |
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| SubjectTerms | Chemistry Chemistry, Inorganic & Nuclear Chemistry, Organic Chemistry, Physical Physical Sciences Science & Technology |
| Title | The application of quasi-enantiomeric trianglamine macrocycles as chiral probes for anion recognition in ion trap ESI mass spectrometry |
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