1982
DOI: 10.1002/chin.198209081
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: NOVEL PACKING MATERIAL FOR OPTICAL RESOLUTION: (+)‐POLY(TRIPHENYLMETHYL METHACRYLATE) COATED ON MACROPOROUS SILICA GEL

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2000
2000
2000
2000

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(3 citation statements)
references
References 1 publication
0
3
0
Order By: Relevance
“…These CSPs are made by using either a polymeric structure or a small ligand (MW < 3000) as the chiral selector. The polymeric CSPs include synthetic chiral polymers [2] and naturally occurring chiral structures [3][4][5]. The most commonly used natural polymers include proteins and carbohydrates (cellulose and amylose).…”
Section: Introductionmentioning
confidence: 99%
“…These CSPs are made by using either a polymeric structure or a small ligand (MW < 3000) as the chiral selector. The polymeric CSPs include synthetic chiral polymers [2] and naturally occurring chiral structures [3][4][5]. The most commonly used natural polymers include proteins and carbohydrates (cellulose and amylose).…”
Section: Introductionmentioning
confidence: 99%
“…Proteins are well-known, naturally occurring chiral polymers. Bonded-protein chiral stationary phases used to play an essential role in the analytical separations of enantiomers during the 1980s [82][83][84], They are always used in the reversed-phase mode. Table 1.2 lists all protein-based chiral stationary phases which are commercially available [85].…”
Section: Proteinsmentioning
confidence: 99%
“…are available as chiral stationary phases coated on wide-pore silica gel. They are polymerized in the presence of a chiral catalyst rather than made from chiral monomers [82].…”
Section: Synthetic Polymeric Chiral Stationary Phasesmentioning
confidence: 99%