A mechanistic rationalization of unusual kinetic behavior in proline-mediated C–O and C–N bond-forming reactions

Literature Information

Publication Date 2006-08-31
DOI 10.1039/B609926B
Impact Factor 6.222
Authors

Suju P. Mathew, Martin Klussmann, Hiroshi Iwamura, David H. Wells, Jr., Alan Armstrong


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Abstract

Kinetic evidence supports the role of the reaction product in the catalytic cycle of proline-mediated α-aminoxylation and α-amination reactions, providing both design principles as well as a model for the evolution of efficiency in catalysis.

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