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1）Su, Y., Petersen,
J. L.,Gregg, T. L.,Shi, X.*, “Ambient 1,2,3-Triazole Ring Opening through
Intermolecular Radical Addition to Vinyl-Triazole.” Org. Lett., 2015, 17, 1208-1211.；
2）Dong, B.‡, Su, Y.‡, Ye, X., Petersen,
J. L., Shi, X.*, “Synthesis and Characterization of
Fluorescent-Active Triazole-Gold Complexes.” Sci. China Chem., 2015, 58, 1-4.；
3）Su, Y., Lu,
M., Dong, B., Chen, H.*, Shi, X.* “Silver Catalyzed Alkyne Activation:
the Surprising Ligand Effect” Adv. Syn. Cat., 2014, 356,
692-696.；
4）Su, Y., Zhang,
Y., Akhmedov, N. G., Petersen, J. L., Shi, X.*, “Ambient Intermolecular
[2 + 2] Cycloaddition: An Example of Carbophilicity and Oxophilicity
Competition in Au/Ag Catalysis.” Org. Lett., 2014, 16,
2478-2481.；
5）Xi, Y.‡, Su, Y.‡, Yu, Z., Dong, B.,
McClain, E. J., Yu, L.*, Shi, X.*, “Chemoselective Carbophilic Addition
of α-Diazoesters through Ligand-Controlled Gold Catalysis.” Angew.
Chem. Int. Ed., 2014, 53, 9817-9821；
6) Su,
Y.‡, Sun, X.‡, Wu, G., Jiao, N.*, “Catalyst-Controlled Highly
Selective Coupling and Oxygenation of Olefins: A Direct Approach to
Alcohols, Ketones, and Diketone.” Angew. Chem. Int. Ed., 2013, 52, 9808-9812；
7）Su, Y., Jiao,
N.*, “Palladium-Catalyzed Oxidative Heck Reaction.” Curr. Org. Chem., 2011, 15, 3362-3388；
8）Su, Y., Jia, W.,
Jiao, N.*, “Inexpensive Copper/Iron-Cocatalyzed Reactions.” Synthesis, 2011, 1678-1690.；
9）Su, Y., Zhang,
L., Jiao, N.*, “Utilization of Natural Sunlight and Air in the
Aerobic Oxidation of Benzyl Halides.” Org. Lett., 2011, 13,
2168-2171；
10）Su, Y., Jiao,
N.*, “Control of Chemo-, Regio-, and Stereoselectivities in Ligand-Free
Pd-Catalyzed Oxidative Heck Reactions of Arylboronic Acids or
Alkenylboronate with Allyl Esters.” Org. Lett., 2009, 11,
2980-2983.；
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