Abstract
Abstract Polysiloxanes with chiral peptide side chains have been synthesized and used as stationary phases in gas chromatography. With these phases amino acid enantiomers can be separated as N-acyl esters. Due to temperature stability up to 230 °C all protein amino acids can be separated and the racemization of synthetic biologically active peptides controlled. The phases can be used to assign the absolute configuration of amino acids. A variety of other classes of compounds can be separated into their enantiomers using the chiral polysiloxanes, like hydroxy acids, sulfoxides, phosphorous compounds, glycols, atrop isomers, amines and alcohols. Various applications of these phases are described including investigations of enantiomer selectivity in nature.
Dates
Type | When |
---|---|
Created | 10 years, 6 months ago (Feb. 21, 2015, 6:30 a.m.) |
Deposited | 4 years, 2 months ago (June 23, 2021, 8:14 a.m.) |
Indexed | 1 year, 8 months ago (Jan. 4, 2024, 1:03 p.m.) |
Issued | 41 years, 11 months ago (Oct. 1, 1983) |
Published | 41 years, 11 months ago (Oct. 1, 1983) |
Published Online | 11 years, 3 months ago (June 2, 2014) |
Published Print | 41 years, 11 months ago (Oct. 1, 1983) |
@article{Bayer_1983, title={Chirale Erkennung von Naturstoffen an optisch aktiven Polysiloxanen Chiral Recognition of Natural Products on Optically Active Polysiloxanes}, volume={38}, ISSN={0932-0776}, url={http://dx.doi.org/10.1515/znb-1983-1019}, DOI={10.1515/znb-1983-1019}, number={10}, journal={Zeitschrift für Naturforschung B}, publisher={Walter de Gruyter GmbH}, author={Bayer, Ernst}, year={1983}, month=oct, pages={1281–1291} }