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Journal Article

Kinetics of the Chiral Disulfonimide-Catalyzed Mukaiyama Aldol Reaction

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Zhang,  Zhipeng
Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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List,  Benjamin
Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Zhang, Z., & List, B. (2013). Kinetics of the Chiral Disulfonimide-Catalyzed Mukaiyama Aldol Reaction. Asian Journal of Organic Chemistry, 2(11), 957-960. doi:10.1002/ajoc.201300182.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0018-D618-E
Abstract
Making progress: The kinetics of the disulfonimide-catalyzed Mukaiyama aldol reaction have been established by using the reaction progress kinetic analysis (RPKA) method. The reaction is first order with respect to catalyst and silyl ketene acetal, and has an order of 0.55 with respect to the aldehyde, which suggests the reversibility of the binding between the aldehyde and the actual catalyst.