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Abstract

Enantioseparation with Capillary Electrophoresis (CE) as Evidence of Chirality Retention during Kolbe Electrolysis of Amino Acids

Department of Medicinal Chemistry, University of Vienna, Althanstraße 14, 1090, Vienna, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2009, 77(7), 208; https://doi.org/10.3797/scipharm.oephg.21.PO-09
Submission received: 16 April 2009 / Accepted: 16 April 2009 / Published: 16 April 2009

Abstract

The radical Kolbe electrolysis can be applied to synthesize non-proteinogenic amino acids starting from ʟ-glutamic acid (or L-aspartic acid, respectively). Using suitable protecting groups for both amino and carboxy functionalities, the retention of chirality at the α-carbon atom can be expected.

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MDPI and ACS Style

DÖRNER, B.; LACHMANN, B.; KRATZEL, M. Enantioseparation with Capillary Electrophoresis (CE) as Evidence of Chirality Retention during Kolbe Electrolysis of Amino Acids. Sci. Pharm. 2009, 77, 208. https://doi.org/10.3797/scipharm.oephg.21.PO-09

AMA Style

DÖRNER B, LACHMANN B, KRATZEL M. Enantioseparation with Capillary Electrophoresis (CE) as Evidence of Chirality Retention during Kolbe Electrolysis of Amino Acids. Scientia Pharmaceutica. 2009; 77(Posters (PO)):208. https://doi.org/10.3797/scipharm.oephg.21.PO-09

Chicago/Turabian Style

DÖRNER, B., B. LACHMANN, and M. KRATZEL. 2009. "Enantioseparation with Capillary Electrophoresis (CE) as Evidence of Chirality Retention during Kolbe Electrolysis of Amino Acids" Scientia Pharmaceutica 77, Posters (PO): 208. https://doi.org/10.3797/scipharm.oephg.21.PO-09

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