(9)     Kennedy, C. R.;* Lin, S.;* Jacobsen, E. N. “Cation–π interactions in small-molecule catalysis”, Angew. Chem., Int. Ed. 2016, submitted. (* co-first author)

 

(8)     Lin, S.;* Diercks, C. S.;* Zhang, Y.-B.;* Kornienko, N.; Nichols, E. M.; Zhao, Y.; Paris, A. R.; Kim, D.; Yang, P.; Yaghi, O. M.; Chang, C. J. “Covalent organic frameworks comprising cobalt porphyrins for catalytic CO2 reduction in water”, Science 2015, 349, 1208–1213. (* co-first author) [link]

 

(7)     Kornienko, N.; Zhao, Y.; Kley, C.; Zhu, C.; Kim, D.; Lin, S.; Chang, C. J.; Yaghi, O. M.; Yang, P. “Metal-organic frameworks for electrocatalytic reduction of carbon dioxide”, J. Am. Chem. Soc. 2015, 137, 14129–14135. [link]

 

(6)     Rogers, C.; Chen, C.; Pedramrazi, Z.; Omrani, A. A.; Tsai, H.-Z.; Jung, H. S.; Lin, S.; Crommie, M. F.; Fischer, F. R. “Closing the nanographene gap: surface-assisted synthesis of peripentacene from 6,6’-bipentacene precursors”, Angew. Chem., Int. Ed. 2015, 54, 15143–15146. [link]

 

(5)     Zhang, H.; Lin, S.; Jacobsen, E. N. “Enantioselective selenocyclization via dynamic kinetic resolution of seleniranium ions by hydrogen-bond donor catalysts”, J. Am. Chem. Soc. 2014, 136, 16485–16488. [link]

 

(4)     Lin, S.; Jacobsen, E. N. “Thiourea-catalysed ring opening of episulfonium ions with indole derivatives by means of stabilizing non-covalent interactions”, Nature Chem. 2012, 4, 817–824. [link]

 

(3)     Knowles, R. R.; Lin, S.; Jacobsen, E. N. “Enantioselective thiourea-catalyzed polycyclizations”, J. Am. Chem. Soc. 2010, 132, 5030–5032. [link]

 

(2)     Li, Y.-Z.; Li, B.-J.; Lu, X.-Y.; Lin, S.; Shi, Z.-J. “Cross dehydrogenative arylation (CDA) of a benzylic C–H bond with arenes by iron catalysis”, Angew. Chem., Int. Ed. 2009, 48, 3817–3820. [link]

 

(1)     Lin, S.; Song, C.-X.; Cai, G.-X.; Wang, W.H.; Shi, Z.-J. “Intra/Intermolecular direct allylic alkylation via Pd(II)-catalyzed allylic C–H activation”, J. Am. Chem. Soc. 2008, 130, 12901–12903. [link]