Journal article

Publication year: 2008

Pages: 6180-6183

Journal: Angewandte Chemie International Edition

Volume number: 47

Issue number: 33

DOI Link: https://doi.org/10.1002/anie.200800641

Publisher: Wiley

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.

Harvard Citation style: Müller, 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 Citation style: Müller, 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