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with high regioselectivities and good to high yields under mild
thermal conditions. In addition, the method reported here can
be successfully applied to a broad range of carboxylic acids and
hydroxycarbamates.
ASSOCIATED CONTENT
* Supporting Information
■
S
The Supporting Information is available free of charge on the
General procedures, characterization data, and NMR
AUTHOR INFORMATION
Corresponding Authors
■
Author Contributions
†Q.D. and P.L. contributed equally.
(7) (a) Zhang, Y.; Patel, S.; Mainolfi, N. Chem. Sci. 2012, 3, 3196−
3199. (b) Sheng, W.-J.; Ye, Q.; Yu, W.-B.; Liu, R.-R.; Xu, M.; Gao, J.-
R.; Jia, Y.-X. Tetrahedron Lett. 2015, 56, 599−601.
(8) (a) Weaver, J. D.; Recio, A.; Grenning, A. J.; Tunge, J. A. Chem.
Rev. 2011, 111, 1846−1913. (b) Dzik, W. I.; Lange, P. P.; Gooßen, L.
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Notes
The authors declare no competing financial interest.
(9) (a) Becht, J.-M.; Catala, C.; Le Drian, C.; Wagner, A. Org. Lett.
2007, 9, 1781−1783. (b) Gooßen, L. J.; Rodríguez, N.; Linder, C. J.
Am. Chem. Soc. 2008, 130, 15248−15249. (c) Gooßen, L. J.;
Zimmermann, B.; Linder, C.; Rodríguez, N.; Lange, P. P.; Hartung,
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C.; Rodríguez, N.; Lange, P. P. Chem. - Eur. J. 2009, 15, 9336−9349.
(e) Gooßen, L. J.; Lange, P. P.; Rodríguez, N.; Linder, C. Chem. - Eur.
J. 2010, 16, 3906−3909.
ACKNOWLEDGMENTS
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This work was financially supported by the Excellent Young
Scholars Research Fund of Beijing Institute of Technology
(319-0012331518, 3190012331523), the National Natural
Science Foundation of China (21231002, 21276026), and the
973 Program (2014CB932103). We are grateful to Dr. John C.-
G. Zhao at the University of Texas at San Antonio for helpful
discussions.
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662−664. (b) Gooßen, L. J.; Rodríguez, N.; Gooßen, K. Angew. Chem.,
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