Prior to ECUST:
15. Song, Runjiang; Xie, Yongtao*, Jin, Zhicao; Yonggui Robin Chi*. Carbene‐Catalyzed Asymmetric Construction of Atropisomers. Angew. Chem. Int. Ed. 2021, 60, 26026. (co-corresponding author)
14. Xie, Yongtao+; Yang, Xing+; Xu, Jun; Chai, Huifang*; Liu, Hongxia; Zhang, Junmin; Song, Jun; Gao, Yuan *; Jin, Zhicao; Yonggui Robin Chi*. Access to Allene‐Containing Molecules via Enantioselective Reactions of Azolium Cumulenolate Intermediates. Angew. Chem. Int. Ed. 2021, 60, 14817. (co-first author) (hot paper)
13. Yang, Xing+; Xie, Yongtao+; Xu, Jun; Ren, Shichao; Mondal, Bivas; Zhou, Liejin; Tian, Weiyi; Zhang, Xinglong; Hao, Lin; Jin, Zhichao; Yonggui Robin Chi*. Carbene‐Catalyzed Activation of Remote Nitrogen Atoms of (Benz)imidazole‐Derived Aldimines for Enantioselective Synthesis of Heterocycles. Angew. Chem. Int. Ed. 2021, 60, 7906. (co-first author) (hot paper)
12. Xie, Yongtao; Sun, Pengwei; Li, Yuxin; Wang, Siwei; Ye, Mengchun*; Li, Zhengming*. Ligand‐Promoted Iron(III)‐Catalyzed Hydrofluorination of Alkenes. Angew. Chem. Int. Ed. 2019, 58, 7097.
11. Xie, Yongtao; Li, Yuxin; Zhou, Sha; Zhou, Shaa; Zhang, Yan; Chen, Minggui; Li, Zhengming*. AlCl3-Promoted Oxygen Transfer: Selective Oxidation of Sulfides to Sulfoxides. Synlett 2018, 29, 340.
10. Xie, Yongtao; Zhou, Sha; Li, Yuxin; Zhou, Shaa; Chen, Minggui; Wang, Baolei; Xiong, Lixia; Yang, Na; Li, Zhengming*. Design, Synthesis, Biological Evaluation and SARs of Novel N‐Substituted Sulfoximines as Potential Ryanodine Receptor Modulators. Chin. J. Chem. 2018, 36, 129.
9. Xie, Yongtao; Zhou, Biying; Zhou, Sha; Zhou, Shaa; Wei, Wei; Liu, Jingbo; Zhan, Yizhou; Li, Zhengming*; et al. Sulfimine‐Promoted Fast O Transfer: One–step Synthesis of Sulfoximine from Sulfide. ChemistrySelect 2017, 2, 1620.
8. Zhao, Yangyang; Gao, Li; Li, Huangong; Sun, Pengwei; Meng, Fanfei; Zhang, Yan; Xie, Yongtao; Sun, Binqiao; Zhou, Sha; Ma, Yi; Xiong, Lixia; Yang, Na; Li, Yuxin; Li, Zhengming. Synthesis, Insecticidal Activities, and Structure–Activity Relationship of Phenylpyrazole Derivatives Containing a Fluoro-Substituted Benzene Moiety. J. Agric. Food Chem.2020, 68, 11282.
7. Zhou, Shaa; Zhou, Sha; Xie, Yongtao; Meng, Xiangde; Wang, Baolei; Xiong, Lixia; Yang, Na; Li, Zhengming. Synthesis, insecticidal activities and SAR studies of novel anthranilic diamides containing trifluoroethoxyl substituent and chiral amino acid moieties. Chin. Chem. Lett. 2018, 29, 1254.
6. Zhou, Sha; Zhou, Shaa; Xie, Yongtao; Jin, Ru-Yi; Meng, Xiang-De; Zhang, Dong-Kai; Hua, Xue-Wen; Liu, Ming; Wu, Chang-Chun; Xiong, Li-Xia; Zhao, Yu; Li, Zheng-Ming. The exploration of chiral N-cyano sulfiliminyl dicarboxamides on insecticidal activities. Chin. Chem. Lett. 2017, 28, 1499.
5. Zhou, Sha; Meng, Xiangde; Ma, Yi; Xie, Yongtao; Zhao, Yu; Song, Hongjian; Xiong, Lixia; Li, Zhengming; Jin, Ruyi. Synthesis, insecticidal activities and structure-activity relationship study of dual chiral sulfilimines. Mol. Diversity 2017, 21, 915.
4. Meng, Xiangde; Zhou, Sha; Xie, Yongtao; Zhao, Yu; Xiong, Lixia; Zhou, Sha; Li, Zhengming. Design, synthesis and biological activities of novel dual-chiral carbon and sulfur pyridine phthalic acid diamide derivatives. Chin. J. Org. Chem. 2017, 37, 908.
3. Liu, Jingbo; Li, Yuxin; Zhang, Xiulan; Cheng, Dandan; Wei, Wei; Wu, Changchun; Xie, Yongtao; Xiong, Lixia; Li, Zhengming. Design, Synthesis, Biological Evaluation and SARs of Novel Anthranilic Diamide Derivatives Containing Amide, Carbamate, Urea, and Thiourea Moieties. Chin. J. Chem. 2017, 35, 368.
2. Wei, Wei; Zhou, Shaa; Cheng, Dandan; Li, Yuxin; Liu, Jingbo; Xie, Yongtao; Li, Yonghong; Li, Zhengming. Design, synthesis and herbicidal activity study of aryl 2,6-disubstituted sulfonylureas as potent acetohydroxyacid synthase inhibitors. Bioorg. Med. Chem. Lett. 2017, 27, 3365.
1. Zhou, Shaa; Zhou, Sha; Hua, Xuewen; Wei, Wei; Xie, Yongtao; Chen, Minggui; Meng, Xiangde; Liu, Ming; Xiong, Lixia; Yang, Na; Wang, Baolei; Li, Zhengming. Design, Synthesis and Insecticidal Evaluation of Anthranilic Diamides Containing Optically Pure Amino Acid Moiety. Chin. J. Chem. 2016, 34, 1218.