2008
DOI: 10.1016/j.jchromb.2008.07.016
|View full text |Cite
|
Sign up to set email alerts
|

A mixed stationary phase containing two versatile cyclodextrin-based selectors for the simultaneous gas chromatographic enantioseparation of racemic alkanes and racemic α-amino acid derivatives☆

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
5
0

Year Published

2010
2010
2015
2015

Publication Types

Select...
4
3
2

Relationship

0
9

Authors

Journals

citations
Cited by 15 publications
(5 citation statements)
references
References 34 publications
0
5
0
Order By: Relevance
“…Whereas permethylated Chirasil-␥-Dex provided only few baseline enantioseparations, permethylated Chirasil-␣-Dex and Chirasil-␤-Dex 5 exhibited complementary behaviour which may indicate the need of employing the two selectors in one CSP as proposed previously [36]. By mixing the two versatile CD selectors octakis ( [83] and heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-␤-cyclodextrin in the polysiloxane PS 086, a comprehensive enantioselectivity spectrum for racemic unfunctionalized alkanes, racemic derivatized ␣-amino acids, lactones, diols, secondary alcohols, ketones and terpenes has been achieved [84].…”
Section: Chiral Stationary Phases Derived From Modified Cyclodextrinsmentioning
confidence: 99%
“…Whereas permethylated Chirasil-␥-Dex provided only few baseline enantioseparations, permethylated Chirasil-␣-Dex and Chirasil-␤-Dex 5 exhibited complementary behaviour which may indicate the need of employing the two selectors in one CSP as proposed previously [36]. By mixing the two versatile CD selectors octakis ( [83] and heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-␤-cyclodextrin in the polysiloxane PS 086, a comprehensive enantioselectivity spectrum for racemic unfunctionalized alkanes, racemic derivatized ␣-amino acids, lactones, diols, secondary alcohols, ketones and terpenes has been achieved [84].…”
Section: Chiral Stationary Phases Derived From Modified Cyclodextrinsmentioning
confidence: 99%
“…Subsequently, in a number of papers the use of mixed binary CD selector systems for the enantioseparation of different classes of chiral compounds has been described [79,[100][101][102][103][104][105]. Recently, a comprehensive enantioselectivity spectrum toward racemic unfunctionalized alkanes and racemic derivatized α-amino acids as well as to other classes of racemic compounds, such as lactones, diols, secondary alcohols, ketones, and terpenes, has been realized by diluting the two versatile CD selectors octakis(6-O-methyl-2,3-di-O-pentyl)-γ-cyclodextrin (Lipodex G) [81] and heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin [87] in the polysiloxane PS-086 [106].…”
Section: Chiral Stationary Phases Based On Modified Cyclodextrins Formentioning
confidence: 99%
“…Enhancement of aqueous solubility of a poorly water-soluble cyclic undecapeptide 7 and a potent glucocorticoid steroid 8 using respectively α-CD/HP-β-CD mixtures and α-CD/HP-γ-CD mixtures is along the same lines. Such synergistic effects between different CDs have also been highlighted when mixed GC stationary phases consisting of two different CD derivatives were used in resolving enantiomers [9][10][11][12] or in positional isomers compounds separation. 13,14 In the field of aqueous organometallic catalysis, CDs are mainly used as mass transfer promoters between aqueous and organic layers by forming inclusion complexes with the substrate.…”
Section: Introductionmentioning
confidence: 95%