科研情況: ? 主要研究方向: 1、基于導向策略的惰性鍵活化研究; 2、碳氫鍵活化及其應用; 3、廉價金屬催化的烯烴雙官能化研究; ? 近5年科研項目: 1、國家自然科學基金面上項目(21801023),鐵催化有機鎂試劑參與的烯烴雙官能化反應研究,執(zhí)行時間:2019.01-2021.12;已結(jié)題,主持。 2、湖南省自然科學基金青年項目(2019JJ50635),格氏試劑對非活化烯烴的加成反應研究,執(zhí)行時間:2019.01-2021.12;已結(jié)題,主持。 3、長沙市自然科學基金一般項目(kq2004070),廉價過渡金屬催化的格氏試劑參與的烯烴雙官能化研究,2020.09-2022.08;在研,主持。 4、湖南省科技廳項目(2018RS3076),湖湘高層次人才聚集工程—創(chuàng)新人才;執(zhí)行時間:2018.10-2021.10;結(jié)題,主持。 ? 近5年科研論文: 1. Dachao Wang, Xiaoting Gan, Lewei Zhou, Hanyu Shu, and Jun Zhou*. Synthesis of Functionized N-arylbenzotriazoles via Palladium Catalyzed Intramolecular Amination. Tetrahedron Letters 2022,88,153587. 2. Jun Zhou, Xin Li, Gang Liao, Bing-Feng Shi*. Rhodium(III)-Catalyzed C–H Vinylation of Arenes: Access to Functionalized Styrenes. Chin. J. Chem. 2018, 36, 1143. 3. Wes Lee, Jun Zhou, Osvaldo Gutierrez*. Mechanism of Nakamura’s Bisphosphine Iron-Catalyzed Asymmetric C(sp2)-C(sp3) Cross-Coupling Reaction: The Role of Spin in Controlling Arylation Pathways. J. Am. Chem. Soc. 2017, 139, 16126. 4. Jun Zhou, Bo Li, Zhen-Chao Qian, Bing-Feng Shi*. Rh(III)-Catalyzed Oxidative Olefination of Picolinamides: Convenient Synthesis of 3-Alkenylpicolinamides, Adv. Synth. Catal. 2014, 356, 1038. 5. Jun Zhou, Bo Li, Fang Hu, Bing-Feng Shi*. Rhodium(III)-Catalyzed Oxidative Olefination of Pyridines and Quinolines: Multigram-Scale Synthesis of Naphthyridinones, Org. Lett. 2013, 15, 3460. 6. Jun Zhou, Weijun Yang, Binjie Wang, Hongjun Ren*. Friedel-Crafts Arylation for the Formation of C(sp2)-C(sp2) Bond: an Efficient Route to Unsymmetrical and Functionalized Polycyclic Aromatic Hydrocarbons (PAHs) from Aryl Triazenes, Angew. Chem. Int. Ed. 2012, 51, 12293. 7. Jun Zhou, Jianjun He, Binjie Wang, Weijun Yang, Hongjun Ren*. 1,7-Palladium Migration via C-H Activation, Followed by Intramolecular Amination: Regioselective Synthesis of Benzotriazoles, J. Am. Chem. Soc. 2011, 133, 6868. ? 專利與成果轉(zhuǎn)化: 1、 史炳鋒,周俊,李博, 一種3位烯基吡啶衍生物的合成方法,中國發(fā)明專利, 授權(quán)公告號:CN103113291B. 2、周俊,王大超,一種鈀催化N-芳基苯并三氮唑衍生物的合成方法,中國發(fā)明專利,公開號:CN113582936A. |