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Organic Letters|January 3, 2023
Applications of the DIB-BBr3 Protocol in Bromination ReactionsLiangkun Pan, Ka-Mei Lee, Yung-Yin Chan, et al.Journal of the American Chemical Society|September 25, 2012
Efficient medium ring size bromolactonization using a sulfur-based zwitterionic organocatalystYi An Cheng, Tao Chen, Chong Kiat Tan, et al.Chemical Communications (Cambridge, England)|October 18, 2012
Enantioselective synthesis of 2-substituted and 3-substituted piperidines through a bromoaminocyclization processLing Zhou, Daniel Weiliang Tay, Jie Chen, et al.Bioorganic & Medicinal Chemistry Letters|October 21, 2025
Synthesis and antitumor activities of quaternary carbon-containing selenolactonesDanqing Li, Yumiao Zhen, Ran Tang, et al.Organic Letters|December 2, 2021
Access to Bromo-γ-butenolides via Zwitterion-Catalyzed Rearrangement of Cyclopropene Carboxylic AcidsRong-Bin Hu, Shengsheng Qiang, Yung-Yin Chan, et al.Organic Letters|March 7, 2013
Lewis basic selenium catalyzed chloroamidation of olefins using nitriles as the nucleophilesDaniel Weiliang Tay, Ivan Tan Tsoi, Jun Cheng Er, et al.Organic Letters|May 12, 2018
Enantioselective Bromolactonization of Deactivated Olefinic AcidsXiaojian Jiang, Shenghui Liu, Si Yang, et al.Journal of Cellular Biochemistry|June 27, 2013
Characterization of miR-210 in 3T3-L1 adipogenesisWei-Cheng Liang, Yan Wang, David Chi-Cheong Wan, et al.Journal of the American Chemical Society|August 5, 2021
A Catalyst-Controlled Enantiodivergent BromolactonizationYuk-Cheung Chan, Xinyan Wang, Ying-Pong Lam, et al.Angewandte Chemie (International Ed. in English)|August 11, 2025
Unveiling an Alternative Mechanism for Lewis Basic Selenium as a C─H Hydrogen Bond Catalyst and Its Application in the Halogenation of ArenesJingxian Huang, Qingyu Zhang, Haihui Wang, et al.Pageof 11