常文举
日期:2023-08-11 阅读次数: 作者: 来源:

   

    姓名:常文举

性别:男

职称:

学历:博士

专业:有机化学

电子邮件:wenjuchang@fzu.edu.cn

研究方向:有机超分子化学,反应机理研究



教育与工作经历

2023.06 至今 南粤26选5开奖结果

2019.07 2023.05  南京大学 特聘副研究员

2014.09 2019.06  南京大学 博士,导师:梁勇教授

2010.09 2014.06  西北师范大学 本科,导师:霍聪德教授


科研简介


科研项目


代表性论文

  1.  Yu, S.;# Chang, W.;# Hua, R.;# Jie, X.; Zhang, M.; Zhao, W.; Chen, J.; Zhang, D.; Qiu, H.;* Liang, Y.;* Hu, W.* "An enantioselective four-component reaction via assembling two reaction intermediates" Nat. Commun. 2022, 13, 7088.

  2. Chang, W.;# Chen, Y.;# Lu, S.;# Jiao, H.; Wang, Y.; Zheng, T.; Shi, Z.; Han, Y.; Lu, Y.; Wang, Y.; Pan, Y.; Yu, J.-Q.; Houk, K. N.; Liu, F.; Liang, Y.* "Computationally designed ligands enable tunable borylation of remote C-H bonds in arenes" Chem 2022, 8, 1775-1788.

  3. Chang, W.;# Wang, Y.;# Chen, Y.;# Ma, J.; Liang, Y.* "Combined computational and experimental exploration of the origin and control in meta-selective C-H borylation of benzamides" Chin. Chem. Lett. 2022, 34, 107879.

  4. Wang, Y.;# Chang, W.;# Qin, S.; Ang, H.; Ma, J.; Lu, S.; Liang, Y.* "Diversification of aryl sulfonyl compounds through ligand controlled meta- and para-C-H borylation" Angew. Chem. Int. Ed. 2022, 61, e202206797. (Hot paper)

  5. Kang, Z.;# Chang, W.;# Tian, X.; Fu, X.; Zhao, W.; Xu, X.;* Liang, Y.;* Hu, W.* "Ternary catalysis enabled three-component asymmetric allylic alkylation as a concise track to chiral α,α-disubstituted ketones" J. Am. Chem. Soc. 2021, 143, 20818-20827.

  6. Chang, W.; Dai, J.; Li, J.; Shi, Y.; Ren, W.; Shi, Y.* "A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid" Org. Chem. Front. 2017, 4, 1074-1078. (HOT articles for 2017)

  7. Chang, W.;# Li, J.;# Ren, W.; Shi, Y.* "Pd-catalyzed regioselective hydro- esterification of 2-allylphenols to seven-membered lactones without external CO gas" Org. & Biomol. Chem. 2016, 14, 3047-3052.

  8. Ren, W.; Chang, W.; Dai, J.; Shi, Y.; Li, J.; Shi, Y.* "An effective Pd-catalyzed regioselective hydroformylation of olefins with formic acid" J. Am. Chem. Soc. 2016, 138, 14864-14867.




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