TY - JOUR
T1 - Tandem reactions combining biocatalysts and chemical catalysts for asymmetric synthesis
AU - Wang, Yajie
AU - Zhao, Huimin
N1 - Funding Information:
This work was supported by U.S. National Science Foundation under the CCI Center for Enabling New Technologies through Catalysis (CENTC) Phase II Renewal, CHE-1205189. Yajie Wang is grateful for a graduate research fellowship from 3M.
Publisher Copyright:
© 2016 by the authors; licensee MDPI, Basel, Switzerland.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - The application of biocatalysts in the synthesis of fine chemicals and medicinal compounds has grown significantly in recent years. Particularly, there is a growing interest in the development of one-pot tandem catalytic systems combining the reactivity of a chemical catalyst with the selectivity engendered by the active site of an enzyme. Such tandem catalytic systems can achieve levels of chemo-, regio-, and stereo-selectivities that are unattainable with a small molecule catalyst. In addition, artificial metalloenzymes widen the range of reactivities and catalyzed reactions that are potentially employable. This review highlights some of the recent examples in the past three years that combined transition metal catalysis with enzymatic catalysis. This field is still in its infancy. However, with recent advances in protein engineering, catalyst synthesis, artificial metalloenzymes and supramolecular assembly, there is great potential to develop more sophisticated tandem chemoenzymatic processes for the synthesis of structurally complex chemicals.
AB - The application of biocatalysts in the synthesis of fine chemicals and medicinal compounds has grown significantly in recent years. Particularly, there is a growing interest in the development of one-pot tandem catalytic systems combining the reactivity of a chemical catalyst with the selectivity engendered by the active site of an enzyme. Such tandem catalytic systems can achieve levels of chemo-, regio-, and stereo-selectivities that are unattainable with a small molecule catalyst. In addition, artificial metalloenzymes widen the range of reactivities and catalyzed reactions that are potentially employable. This review highlights some of the recent examples in the past three years that combined transition metal catalysis with enzymatic catalysis. This field is still in its infancy. However, with recent advances in protein engineering, catalyst synthesis, artificial metalloenzymes and supramolecular assembly, there is great potential to develop more sophisticated tandem chemoenzymatic processes for the synthesis of structurally complex chemicals.
KW - Artificial metalloenzyme
KW - Asymmetric synthesis
KW - Biocatalysis
KW - Chemoenzymatic
KW - Dynamic kinetic resolution
KW - Tandem catalysis
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U2 - 10.3390/catal6120194
DO - 10.3390/catal6120194
M3 - Review article
AN - SCOPUS:85008147421
SN - 2073-4344
VL - 6
JO - Catalysts
JF - Catalysts
IS - 12
M1 - 194
ER -