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Updated: Aug 10, 2026

The Importance of Correct Protein Concentration for Kinetics and Affinity Determination in Structure-function Analysis
Published on: March 17, 2010
Total synthesis of (-)-callystatin A
M Kalesse1, M Quitschalle, C P Khandavalli
1Institut für Organische Chemie, Universität Hannover, Schneiderberg 1B, 30167 Hannover, Germany. kalesse@mbox.oci.uni-hannover.de
Abstract:
[reaction: see text] The enantioselective synthesis of callystatin A is described. The pivotal step in the synthesis is the stereoselective aldol reaction that generates the beta-hydroxy ketone moiety. Utilizing the allylic strain within the ethyl ketone precursor, we were able to generate the all-syn configuration of callystatin A. For the construction of the two diene moieties, both a Heck coupling and a Wittig reaction were employed.
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