Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase

10.1002/chir.10141

Saved in:
Bibliographic Details
Main Authors: Wang, X., Ching, C.B.
Other Authors: CHEMICAL & ENVIRONMENTAL ENGINEERING
Format: Article
Published: 2014
Subjects:
Online Access:http://scholarbank.nus.edu.sg/handle/10635/92086
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: National University of Singapore
id sg-nus-scholar.10635-92086
record_format dspace
spelling sg-nus-scholar.10635-920862024-11-10T04:45:52Z Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase Wang, X. Ching, C.B. CHEMICAL & ENVIRONMENTAL ENGINEERING β-cyclodextrin Enantiomeric separation Enthalpy and entropy of binding to CSP High-performance liquid chromatography (HPLC) Mobile phase effects Nadolol 10.1002/chir.10141 Chirality 14 10 798-805 CHRLE 2014-10-09T09:55:33Z 2014-10-09T09:55:33Z 2002 Article Wang, X., Ching, C.B. (2002). Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase. Chirality 14 (10) : 798-805. ScholarBank@NUS Repository. https://doi.org/10.1002/chir.10141 08990042 http://scholarbank.nus.edu.sg/handle/10635/92086 000178965300005 Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic β-cyclodextrin
Enantiomeric separation
Enthalpy and entropy of binding to CSP
High-performance liquid chromatography (HPLC)
Mobile phase effects
Nadolol
spellingShingle β-cyclodextrin
Enantiomeric separation
Enthalpy and entropy of binding to CSP
High-performance liquid chromatography (HPLC)
Mobile phase effects
Nadolol
Wang, X.
Ching, C.B.
Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
description 10.1002/chir.10141
author2 CHEMICAL & ENVIRONMENTAL ENGINEERING
author_facet CHEMICAL & ENVIRONMENTAL ENGINEERING
Wang, X.
Ching, C.B.
format Article
author Wang, X.
Ching, C.B.
author_sort Wang, X.
title Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
title_short Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
title_full Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
title_fullStr Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
title_full_unstemmed Liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-O-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
title_sort liquid chromatographic retention behavior and enantiomeric separation of three chiral center β-blocker drug (nadolol) using heptakis (6-azido-6-deoxy-2, 3-di-o-phenylcarbamolyted) β-cyclodextrin bonded chiral stationary phase
publishDate 2014
url http://scholarbank.nus.edu.sg/handle/10635/92086
_version_ 1821226079689375744