(Q43611666)

English

Simultaneous separation of the stereoisomers of 1-amino-2-hydroxy and 2-amino-1-hydroxypropane phosphonic acids by stereoselective capillary electrophoresis employing a quinine carbamate type chiral selector

scientific article published in April 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Simultaneous separation of the stereoisomers of 1-amino-2-hydroxy and 2-amino-1-hydroxypropane phosphonic acids by stereoselective capillary electrophoresis employing a quinine carbamate type chiral selector (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

electrophoresis

0 references

stereoselectivity

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Lämmerhofer M

1

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Zarbl E

2

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Lindner W

3

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Peric Simov B

4

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Hammerschmidt F

5

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

publication date

1 April 2001

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Electrophoresis

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

22

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

1182-1187

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Tert.-butylcarbamoylquinine as chiral ion-pair agent in non-aqueous enantioselective capillary electrophoresis applying the partial filling technique

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Enantiomeric separations by nonaqueous capillary electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Enantioresolution of disopyramide by capillary affinity electrokinetic chromatography with human alpha1-acid glycoprotein (AGP) as chiral selector applying a partial filling technique.

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Absolute Konfiguration der (2-Amino-1-hydroxyethyl)phosphonsäure ausAcanthamoeba castellanii (Neff) - Darstellung der Phosphonsäure-Analoga von (+)- und (-)-Serin

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Direct separation of amino acid enantiomers using a chiral crown ether stationary phase. Application to 2-amino-omega-phosphonoalkanoic acids

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Quinine versus carbamoylated quinine-based chiral anion exchangers. A comparison regarding enantioselectivity for N-protected amino acids and other chiral acids

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Enantioselective anion exchangers based on cinchona alkaloid-derived carbamates: influence of C8/C9 stereochemistry on chiral recognition

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Enantiomeric separation of N-protected amino acids by non-aqueous capillary electrophoresis using quinine or tert-butyl carbamoylated quinine as chiral additive

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Enantiomeric resolution study by capillary electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2F1522-2683%28%2922%3A6%3C1182%3A%3AAID-ELPS1182%3E3.0.CO%3B2-O

21 January 2018

Identifiers

10.1002/1522-2683()22:6<1182::AID-ELPS1182>3.0.CO;2-O

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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