何振宇 教授 博士 广东省 研究领域: 精细化工 研究方向: 金属有机化学反应、有机烯烃高分子功能材料、烯烃和芳香族化合物的绿色催化合成 所在单位: 南方科技大学

基本信息

所在单位:
南方科技大学
机构细分:
化学系
单位类型:
高等院校
职务:
教授
职称:
教授
最高学历:
博士
专家介绍:
何振宇,化学系青年教师,Grubbs 研究院双聘教授,广东省突出贡献人员专业技术资格有机化学研究员,广东省高校化学类专业指导委员会委员,马萨诸塞州理工学院(MIT)博士后,在交叉氢烯基化、N-杂环卡宾Ni(II)H催化剂、催化合成支链和偕二取代烯烃、 N-杂环卡宾-过渡金属不对称催化的远程电子效应技术上建立了比较良好的国际声誉,是我国乃至全世界目前在“NHC-Ni” 和“Hydroalkenylation”领域中最优秀的化学家之一,他积极申请各种研究经费,紧追国际前沿,科技创新能力和组织管理效果情况良好。


论文获亮点报道总计>30次,获7项国际奖项(ACS, RSC, Thieme, ACP颁发),常应邀作国际研讨会报告(超过35次海外邀请讲座和演讲,如: 入选中国-意大利有机化学双边研讨会的10人代表团)和撰写综述(Prof. Scott Miller, Yale & Dieter Enders, RWTH),他已通过国内外专家和学术委员会评估并获得了tenure, 并已被邀请为北海道大学短期兼职讲师。是一个具有明确发展目标和动力为社会做出贡献的青年研究学者。

科研能力

研究领域:
精细化工
研究方向:
金属有机化学反应、有机烯烃高分子功能材料、烯烃和芳香族化合物的绿色催化合成
英文标签:
Nickel;N-heterocyclic Carbenes;Hydroalkenylation;Asymmetric Catalysis;Olefins;Asymmetric Epoxidation;Heterocycles;Oxidative Coupling;Nickel-catalyzed;Insertion
论文著作:
(20)(NHC)NiH-Catalyzed Regiodivergent Cross-Hydroalkenylation of Vinyl Ether with α-Olefin: 1,2- and 1,3-Disubstituted Allyl Ether Syntheses. Chen, W.; Li, Y.; Chen, Y.; Ho, C.-Y.* Angew. Chem. Int. Ed. 2018, 57, 2677. (Highlighted in X-mol & Chin. J. Org.Chem.)

(19)(NHC)NiH-Catalyzed Intermolecular Regio- and Diastereoselective Cross-Hydroalkenylation of Endocyclic Dienes with α-Olefins. Lian, X.; Chen, W.; Dang, L.; Li, Y.; Ho, C.-Y.* Angew. Chem. Int. Ed. 2017, 56, 9048. (Highlighted in X-mol.)

(18)Mechanism and Regioselectivities of (NHC)Nickel(II)hydride-Catalyzed Cycloisomerization of Dienes: A Computational Study. Gao, Y.; Houk, K. N.; Ho, C.-Y.*; Hong, X.* Org. Biomol. Chem. 2017, 15, 7131. Themed Collections: Mechanistic Aspects of Organic Synthesis

(17)Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic Effects of Substrates and Chiral N-Heterocyclic Carbene Ligands Ho, C.-Y.*; Chan, C.-W.; He, L. Angew. Chem. Int. Ed. 2015, 54, 4512.
Featured as Front Cover & VIP (Very Important Paper),
in Angew. Chem. Int. Ed. 2015, 54 (15), 4403.
in ChemCatChem 2015, 7, 1639 by Prof. Gerhard Hilt &
in ChemInform (preparative org. chem.) & in X-Mol.

(16)Substituted 1,3-cyclohexadiene synthesis by NHC-Nickel(0) catalyzed [2+2+2] cycloaddition of 1,n-Enyne”. Zhao, J.-P.; Chan, S.-C.; Ho, C.-Y.* Tetrahedron 2015, 71, 4426. Invited Special Symposium-in-Print: Progress in organic synthesis: New reactions, strategies and targets.

(15)Computational Exploration of Mechanism and Selectivities of NHC-Ni(II)hydride Catalyzed Hydroalkenylations of Styrene with a-Olefins. Hong, X.; Wang, J.; Yang, Y.-F.; He, L.; Ho, C.-Y.*; Houk, K. N.* ACS Catal. 2015, 5, 5545.

(14)Nitrate-Enhanced NHC-NiH Catalyzed Tail-to-Tail Vinyl Ether Dimerization. He, L.; Ho, C.-Y.* Synlett 2014, 25, 2738. (Invited Special Issue: Catalysis with Sustainable Metals.)

(13)Medium-Sized Heterocycle Synthesis by the Use of Synergistic Effects of Ni-NHC and γ Coordination in Cycloisomerization. Ho, C.-Y.*; He, L. J. Org. Chem. 2014, 79, 11873.
Highlighted thrice:
in SynFacts 2014, 10, 913 (by Prof. V. Snieckus)
in ChemInform (preparative org. chem.)
in Organic Chemistry Highlights, 2015(by Prof. D. F. Taber)“C-O Ring Construction”

(12)Synthesis, biological activity, and biopharmaceutical characterization of tacrine dimers as acetylcholinesterase inhibitors. Qian, S.; He, L.; Mak, M.; Han, Y.*; Ho, C.-Y.*; Zuo, Z.* Int. J. Pharmaceutics, 2014, 477, 442.

(11)Shuffle off the Classic b-Si Elimination by Ni-NHC Cooperation: Implication for C-C Forming Reactions Involving Ni-Alkyl-β-Silanes. Ho, C.-Y.*; He, L. Chem. Commun. 2012, 48, 1481.
Highlighted twice:
in Novo Nordisk & in ChemInform (Organoelement compounds)

(10)Catalytic Intermolecular Tail-to-Tail Hydroalkenylation of Styrenes with alpha Olefins: Regioselective Migratory Insertion Controlled by a Nickel/N-Heterocyclic Carbene. Ho, C.-Y.*; He, L. Angew. Chem. Int. Ed. 2010, 49, 9182.
Highlighted thrice:
in SynForm 2011, issue 2, A15-16 & as Cover (by Prof. M. Zanda);
in SynFacts 2011, issue 3, 310 (by Prof. P. Knochel);
in Organic Chemistry Highlights, 2011 Functionalization & Homologation of Alkenes (by Prof. D. F. Taber)

(9)Cyanative Alkene-Aldehyde Coupling: Ni(0)-NHC-Et2AlCN Mediated Chromanols Synthesis with High cis-Selectivity at room temperature. Ho, C.-Y.* Chem. Commun. 2010, 46, 466.

(8)Nitrile assisted, Bronsted acid catalyzed regio and stereoselective diarylphosphonylation of allyl silyl ethers. Ho, C.-Y.*; Chan, C.-W.; Wo, S.-K.; Zuo, Z.; Chan, L.-Y. Biomol. Chem. 2010, 8, 3480. (Highlighted in ChemInform (organoelement compounds))

(7)Alpha Olefins as Alkenylmetal Equivalents in Catalytic Conjugate Addition Reactions. Ho, C.-Y.; Ohmiya, H.; Jamison, T. F.* Angew. Chem. Int. Ed. 2008, 47, 1893.

(6)Highly Chemoselective Reductive Amination of Carbonyl Compounds Promoted by InCl3/Et3SiH/MeOH System. Lee, O.-Y.; Law, K.-L.; Ho, C.-Y.; Yang, D.* J. Org. Chem. 2008, 73, 8829.

(5)Highly Selective Coupling of Alkenes and Aldehydes Catalyzed by NHC–Ni–P(OPh)3: Synergy Between a Strong σ-Donor and a Strong π-Acceptor. Ho, C.-Y.; Jamison, T. F.* Angew. Chem. Int. Ed. 2007, 46, 782.
Highlighted twice:
in Angew. Chem. Int. Ed. as Hot Paper
in ChemInform (isocyclic compounds)

(4)Nickel-Catalyzed Coupling of Alkenes, Aldehydes, and Silyl Triflates. Ng, S.-S.; Ho, C.-Y.; Jamison, T. F.* J. Am. Chem. Soc. 2006, 128, 11513.

(3)Nickel-Catalyzed, Carbonyl-Ene-Type Reactions: Selective for Alpha Olefins and More Efficient with Electron-Rich Aldehydes. Ho, C.-Y.; Ng, S.-S.; Jamison, T. F.* J. Am. Chem. Soc. 2006, 128, 5326. Highlighted in ChemInform (isocyclic compounds)

(2)Fluorinated Chiral Secondary Amines as Catalysts for Epoxidation of Olefins with Oxone. Ho, C.-Y.; Chen, Y.-C.; Wong, M.-K.; Yang, D.* J. Org. Chem. 2005, 70, 898.

(1)Asymmetric epoxidation of olefins catalyzed by chiral iminium salts generated in-situ from chiral amines and aldehydes. Wong, M.-K.; Ho, L.-M.; Zheng, Y.-S.; Ho, C.-Y.; Yang, D.* Org. Lett. 2001, 3, 2587.
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