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tions, many aromatic aldehydes and cyclic ketones could partici-
pate in the reaction with high yields and moderate
stereoselectivity. Though the stereoselectivitives are not satisfac-
tory, this system may be developed into a potentially worthy
method for enzyme promiscuity study.
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Acknowledgments
We gratefully acknowledge the National Natural Science Foun-
dation of China (No. 21001077; 20121001), Program for Changji-
ang Scholars and Natural Science Foundation of Jiangxi (No.
20114BAB213003; 20122BAB203006) for financial support. We
also thank the Sichuan University Analytical & Testing Center for
NMR analysis.
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Supplementary data
Supplementary data associated with this article can be found,
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