个人简述：

联系方式：

984816350@qq.com    haibiny@gdut.edu.cn

教育背景：

2004/09-2008/07，湖南师范大学，药学，学士

2010/09-2015/07，中科院上海有机化学研究所，有机化学，博士，导师：施敏研究员

科研经历：

2011/06-2015/07，中国科学院上海有机化学研究所，金属有机化学国家重点实验室，导师：施敏研究员

2015/10-2017/10，瑞典斯德哥尔摩大学，有机化学系，博士后，合作导师：Nicklas Selander教授

2017/10-2018/12，美国加州大学河滨分校，化学系，博士后，合作导师：David B.C. Martin教授

研究领域：

(1)光介导的自由基反应

(2)不对称催化

(3)过渡金属催化的新型有机化学反应

科研项目：

1、瑞典Wenner-Gren基金，铁催化的新型偶联反应及配体设计，2015-2017，60万克朗，已结题。

代表性论文及著作：

[1] Yang, H.-B.; Feceu, A.; Martin, D. B. C. * “Catalyst-Controlled C–H Functionalization of Adamantanes using Selective H-Atom Transfer”. Submitted. [ChemRxiv preprint].

[2] Yang, H.-B.; Pathipati, S. R.; Selander, N.* “Nickel-Catalyzed 1,2-Aminoarylation of Oxime Ester-Tethered Akenes with Boronic Acids”. ACS Catal. 2017, 7, 8441-8445. (JCR一区, top期刊).

[3] Yang, H.-B.; Selander, N.* “Divergent Iron-Catalyzed Coupling of O-Acyloximes with Silyl Enol Ethers”. Chem. Eur. J.2017, 23, 1779-1783. (JCR二区, top期刊)

Highlighted in Synfacts (2017, 13, 0350);ESI “Highly Cited Paper”.

[4] Yang, H.-B.; Selander, N.* “A redox-economical synthesis of trifluoromethylated enamides with the Langlois reagent”. Org.Biomol. Chem. 2017, 15, 1771-1775. (JCR二区)

[5] Yang, H.-B.; Yuan, Y.-C.; Wei, Y.*; Shi, M.* “Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes”. Chem. Commun. 2015, 51, 6430-6433. (JCR一区, top期刊)

[6] Yang, H.-B.; Zhao, Y.-Z.; Sang, R.; Wei, Y.*; Shi, M.*, “Asymmetric Synthesis of Bioxindole-Substituted Hexahydrofuro[2,3-b]furans via Hydroquinine Anthraquinone-1,4-diyl Diether-Catalyzed Domino Annulation of Acylidenoxindoles/Isatins,Acylidenoxindoles and Allenoates”. Adv. Synth. Catal. 2014, 356, 3799-3808. (JCR一区, top 期刊)

[7] Yang, H.-B.; Zhao, Y.-Z.; Sang, R.; Shi, M.*, “(DHQ)₂AQN-Catalyzed Asymmetric Substitution of Isatin-Derived Hydrazones with O-Boc-Protected Morita-Baylis-Hillman Adducts: A Strategy for Synthesizing Enantioenriched Azo Compounds Incorporating an Oxindole Scaffold”. J. Org. Chem .2014, 79, 3519-3528. (JCR 二区, top 期刊)

[8] Yang, H.-B.; Fan, X.; Wei, Y.*; Shi, M.*, “Solvent-controlled nucleophilic trifluoromethylthiolation of Morita–Baylis–Hillman carbonates: dual roles of DABCO in activating the Zard’s trifluoromethylthiolation reagent and the MBH carbonates”. Org. Chem. Front. 2015, 2, 1088-1093. (JCR 二区)

[9] Yang, H.-B.; Guan, X.-Y.; Wei, Y., Shi, M.*, “A Three-Component Condensation for the Construction of the Spiro[indoline-3,3′-piperidin]-2-one Skeleton”. Eur. J. Org. Chem. 2012, 2792-2800. (JCR 三区)

[10] Yang, H.-B.; Zhao, Y.-Z.; Sang, R.; Tang, X.-Y., Shi, M.*, “A novel multicomponent reaction involving isoquinoline, allenoate and activated ketone”. Tetrahedron, 2013, 69, 9205-9211. (JCR 三区)

[11] Yang, H.-B.; Wei, Y.*; Shi, M.*, “Construction of spiro[indoline]oxindoles through one-pot thermal-induced [3+2] cycloaddition/silica gel-promoted fragmentation sequence between isatin ketonitrones and electron-deficient alkynes”. Tetrahedron, 2013, 69, 4088-4097. (JCR 三区)

[12] Yang, H.-B.; Shi, M.*, “Yb(NTf₂)₃-catalyzed [3+3] cycloaddition between isatin ketonitrones and cyclopropanes to construct novel spiro[tetrahydro-1,2-oxazine]oxindoles”. Org. Biomol. Chem. 2012, 10, 8236-8243. (JCR二区)