2007
DOI: 10.1016/j.cclet.2007.09.016
|View full text |Cite
|
Sign up to set email alerts
|

A chiral stationary phase with special hydrophobic framework for ligand-exchange chromatography

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2009
2009
2010
2010

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 4 publications
0
1
0
Order By: Relevance
“…Ligand exchange CSPs have been extensively studied and used in resolving racemic analytes, which can be used as bidentate ligands such as ␣-amino acids, since the pioneering works of Davankov [15][16][17][18][19]. We also developed ligand exchange CSPs by bonding (S)-leucinol derivative, sodium N-[(S)-1-hydroxymethyl-3-methylbutyl]-N-undecylaminoacetate, or (R)-phenylglycinol derivative, sodium N-[(R)-2-hydroxy-1-phenylethyl]-N-undecylaminoacetate, to silica gel [20,21].…”
Section: Introductionmentioning
confidence: 99%
“…Ligand exchange CSPs have been extensively studied and used in resolving racemic analytes, which can be used as bidentate ligands such as ␣-amino acids, since the pioneering works of Davankov [15][16][17][18][19]. We also developed ligand exchange CSPs by bonding (S)-leucinol derivative, sodium N-[(S)-1-hydroxymethyl-3-methylbutyl]-N-undecylaminoacetate, or (R)-phenylglycinol derivative, sodium N-[(R)-2-hydroxy-1-phenylethyl]-N-undecylaminoacetate, to silica gel [20,21].…”
Section: Introductionmentioning
confidence: 99%