Journalartikel

Jahr der Veröffentlichung: 2010

Seiten: 2689-2690

Zeitschrift: Chemical Communications

Bandnummer: 46

Heftnummer: 15

DOI Link: https://doi.org/10.1039/C001075H

Verlag: Royal Society of Chemistry

Abstract: 

We describe the efficient and highly enantioselective kinetic resolution of trans-cycloalkane-1,2-diols
utilizing an enantioselective Steglich reaction with a variety of
carboxylic acids that form the corresponding anhydrides in situ.

Harvard-Zitierstil: Hrdina, R., Müller, C. and Schreiner, P. (2010) Kinetic resolution of trans-cycloalkane-1,2-diols via Steglich esterification, Chemical Communications, 46(15), pp. 2689-2690. https://doi.org/10.1039/C001075H

APA-Zitierstil: Hrdina, R., Müller, C., & Schreiner, P. (2010). Kinetic resolution of trans-cycloalkane-1,2-diols via Steglich esterification. Chemical Communications. 46(15), 2689-2690. https://doi.org/10.1039/C001075H