Journalartikel

Enantioselective Kinetic Resolution of trans‐Cycloalkane‐1,2‐diols


AutorenlisteMüller, CE; Wanka, L; Jewell, K; Schreiner, PR

Jahr der Veröffentlichung2008

Seiten6180-6183

ZeitschriftAngewandte Chemie International Edition

Bandnummer47

Heftnummer33

DOI Linkhttps://doi.org/10.1002/anie.200800641

VerlagWiley


Abstract

Finally! The title resolution is achieved with a nonnatural,
partially rigid, lipophilic tetrapeptide at low catalyst loadings
without additional base or cosolvents. The transition‐state model
(ball‐and‐stick model in the scheme; C gray, N blue, O red) emphasizes
the interplay between hydrogen‐bonding and hydrophobic interactions.




Zitierstile

Harvard-ZitierstilMüller, C., Wanka, L., Jewell, K. and Schreiner, P. (2008) Enantioselective Kinetic Resolution of trans‐Cycloalkane‐1,2‐diols, Angewandte Chemie International Edition, 47(33), pp. 6180-6183. https://doi.org/10.1002/anie.200800641

APA-ZitierstilMüller, C., Wanka, L., Jewell, K., & Schreiner, P. (2008). Enantioselective Kinetic Resolution of trans‐Cycloalkane‐1,2‐diols. Angewandte Chemie International Edition. 47(33), 6180-6183. https://doi.org/10.1002/anie.200800641



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