Journalartikel

En route to multicatalysis: kinetic resolution of trans-cycloalkane-1,2-diols via oxidative esterification


AutorenlisteHofmann, C; Schuler, SMM; Wende, RC; Schreiner, PR

Jahr der Veröffentlichung2014

Seiten1221-1223

ZeitschriftChemical Communications

Bandnummer50

Heftnummer10

DOI Linkhttps://doi.org/10.1039/C3CC48584F

VerlagRoyal 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.




Zitierstile

Harvard-ZitierstilHofmann, 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-ZitierstilHofmann, 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



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