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2004 | 3 |
2011 | 2 |
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Page 1
Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N-allylamino-6A-deoxy)-perfunctionalized beta-cyclodextrin and covalently bonded silica gel.
J Chromatogr A. 2004 Mar 26;1031(1-2):135-42. doi: 10.1016/j.chroma.2003.11.018.
J Chromatogr A. 2004.
PMID: 15058577
Novel β-cyclodextrin chiral stationary phases with different length spacers for normal-phase high performance liquid chromatography enantioseparation.
Lai X, Tang W, Ng SC.
Lai X, et al.
J Chromatogr A. 2011 Jun 3;1218(22):3496-501. doi: 10.1016/j.chroma.2011.03.071. Epub 2011 Apr 4.
J Chromatogr A. 2011.
PMID: 21507409
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Novel cyclodextrin chiral stationary phases for high performance liquid chromatography enantioseparation: effect of cyclodextrin type.
Lai X, Tang W, Ng SC.
Lai X, et al.
J Chromatogr A. 2011 Aug 19;1218(33):5597-601. doi: 10.1016/j.chroma.2011.06.020. Epub 2011 Jun 17.
J Chromatogr A. 2011.
PMID: 21762924
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Enantioseparation on mono(6A-n-allylamino-6A-deoxy)permethylated 3-cyclodextrin covalently bonded silica gel.
Lai XH, Ng SC.
Lai XH, et al.
J Chromatogr A. 2004 Dec 3;1059(1-2):53-9. doi: 10.1016/j.chroma.2004.07.018.
J Chromatogr A. 2004.
PMID: 15628124
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Preparation and enantioseparation characteristics of two chiral stationary phases based on mono(6(A)-azido-6(A)-deoxy)-perphenylcarbamoylated alpha- and gamma-cyclodextrin.
Lai XH, Bai ZW, Ng SC, Ching CB.
Lai XH, et al.
Chirality. 2004 Nov;16(9):592-7. doi: 10.1002/chir.20052.
Chirality. 2004.
PMID: 15390089
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