Journal article

Publication year: 2014

Pages: 1221-1223

Journal: Chemical Communications

Volume number: 50

Issue number: 10

DOI Link: https://doi.org/10.1039/C3CC48584F

Publisher: Royal Society of Chemistry

Abstract: 

We demonstrate the application of a multicatalyst to the oxidation of a
broad variety of aldehydes and subsequent enantioselective
esterification of the incipient acids with (±)-trans-cycloalkane-1,2-diols.
This reaction operates well with a multicatalyst bearing two
independent catalytic moieties that provide monoprotected 1,2-diols in
one pot.

Harvard Citation style: Hofmann, C., Schuler, S., Wende, R. and Schreiner, P. (2014) En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification, Chemical Communications, 50(10), pp. 1221-1223. https://doi.org/10.1039/C3CC48584F

APA Citation style: Hofmann, C., Schuler, S., Wende, R., & Schreiner, P. (2014). En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification. Chemical Communications. 50(10), 1221-1223. https://doi.org/10.1039/C3CC48584F