何振宇博士于2000年-2005年在香港大学（the university of hong kong）化学系杨丹教授指导下从事有机不对称催化并获得博士学位，随后在麻省理工学院（M.I.T.） prof. timothy f. jamison研究组作为博士后从事过渡金属催化。从2007年底开始，在香港中文大学（the chinese university of hongkong）作为研究助理教授开始了独立的研究，从2013年起，加盟深圳南方科技大学(SUSTech)，入选深圳市孔雀计划b类人员，主要从事金属有机化学n-杂环卡宾及其在有机金属催化中的应用研究，在国内外学术刊物（angew. chem. int. ed, j. am.chem. soc，chem. commun., acs catal.等）发表论文多篇，并获the asian core program lectureship award (from japan)，the asian core program lectureship award (from singapore)等多项奖项。
教育背景：
2000.09-2005.07 —— 博士，香港大学，化学专业 (with Prof. D. Yang)
1997.09-2000.07 —— 学士，香港大学，化学专业
工作经历：
2013.01-至今 —— 副教授，南方科技大学，化学系
2007.09-2013.01 —— 研究助理教授，香港中文大学，化学系
2005.09-2007.07 —— 博士后，麻省理工学院，化学系 (with Prof. T. F. Jamison)
荣誉及奖励：
2017 —— Thieme化学期刊奖；有机化学研究员
2016 —— 深圳市南山区领航人才B类；南方科技大学优秀教学奖；南方科技大学青年教师教学竞赛奖
2015 —— 广东省本科高校化学类专业教学指导委员会委员
2013 —— 深圳市海外高层次人才B类；ACS Excellence in Science Symposium 最佳海报奖
2011 —— 亚洲核心计划讲学奖（新加坡）
2010 —— 亚洲核心计划讲学奖（日本）
2005-2007 —— 裘槎奖学金
新材料产业—先进石化工新材料—专用化学品及材料制造—专用化学品及材料制造
Diastereodivergent Hydrosilylative Enyne Cyclization Catalyzed by N-Heterocyclic Carbene-Ni(0) .Yu, M.; Yong, X.F.; Gao, W.W.; Ho, C.-Y. J. Chem. 2021, 39 , 1587.
NHC/Nickel(II)-Catalyzed [3+2] Cross-Dimerization of Unactivated Olefins and Methylenecyclopropanes. Huang, J.-Q.; Ho, C.-Y., Angewandte Chemie International Edition. 2020, 59 , 5288.
NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross-hydroalkenylation of cyclic 1,3-dienes and heterosubstituted terminal olefins. Chen, Y.; Dang, L.; Ho, C.-Y., Nature Communications. 2020, 11, 2269.
NHC-Ni catalyzed 1,3- and 1,4-diastereodivergent heterocycle synthesis from hetero-substituted enyne. Yong, X.; Gao, W.; Lin, X.; Ho, C.-Y., Communications 2020, 3, 50.
NHC-Ni(0) Catalyzed Diastereodivergent Hydroacylative Enyne Cyclization: Synthesis of Heterocycles bearing gamma-Enone. Advanced Synthesis & Catalysis. Yong, X.; Ng, E.; Zhen, Z.; Lin, X.; Gao, W.; Ho, C.-Y., 2020, 362 , 4164.
Applications of (NHC)Ni(II) Catalyzed [3+2] Hydroalkenylation-Rearrangement Cascades. Yong, X.; Huang, J.-Q., Ho, C.-Y., Chinese Journal of Organic Chemistry. 2020, 40 , 3327. (invited special issue: Prof. Henry N. C. Wong)
[(NHC)(NiH)-H-II]-Catalyzed Cross-Hydroalkenylation of Cyclopropenes with Alkynes: Cyclopentadiene Synthesis by [(NHC)Ni-II]-Assisted C-C Rearrangement. Huang, J.-Q.; Ho, C.-Y, Chem. Int. Ed. 2019, 58, 5702.
Electronic Effects on Chiral NHC–Transition-Metal. Yong, X., Thurston, R. & Ho, C.-Y,Synthesis 2019, 51, 2058.
Synthesis and Study of Au(III)-Indolizine Derivatives: Turn-on Luminescence by Photo-induced Control Release. Yang, J.; Zhu, Y.; Tse, A. K.-W.; Zhou, X.; Chen, Y.; Tse, Y. C.;* Wong, K. M.-C.;* Ho, C.-Y, Commun. 2019, 55, 4471.
(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, Chem. Int. Ed. 2018, 57, 2677.
(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.* Chem. Int. Ed. 2017, 56, 9048.
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.* Biomol. Chem. 2017, 15, 7131.
Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic Effects of Substrates and Chiral N-Heterocyclic Carbene Ligands Ho, C.-Y.*; Chan, C.-W.; He, L. Chem. Int. Ed. 2015, 54, 4512.
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.
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.
Nitrate-Enhanced NHC-NiH Catalyzed Tail-to-Tail Vinyl Ether Dimerization. He, L.; Ho, C.-Y.* 2014, 25, 2738.
Medium-Sized Heterocycle Synthesis by the Use of Synergistic Effects of Ni-NHC and γ‑Coordination in Cycloisomerization. Ho, C.-Y.*; He, L. J. Chem. 2014, 79, 11873.
Shuffle off the Classic -Si Elimination by Ni-NHC Cooperation: Implication for C-C Forming Reactions Involving Ni-Alkyl-β-Silanes. Ho, C.-Y.*; He, L. Commun. 2012, 48, 1481.
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. Chem. Int. Ed. 2010, 49, 9182.
Cyanative Alkene-Aldehyde Coupling: Ni(0)-NHC-Et2AlCN Mediated Chromanols Synthesis with High cis-Selectivity at room temperature. Ho, C.-Y.* Commun. 2010, 46, 466.
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.
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. Org. Chem. 2010, 8, 3480.
Alpha Olefins as Alkenylmetal Equivalents in Catalytic Conjugate Addition Reactions. Ho, C.-Y.; Ohmiya, H.; Jamison, T. F.* Chem. Int. Ed. 2008, 47, 1893.
Highly Chemoselective Reductive Amination of Carbonyl Compounds Promoted by InCl3/Et3SiH/MeOH System. Lee, O.-Y.; Law, K.-L.; Ho, C.-Y.; Yang, D.* Org. Chem. 2008, 73, 8829.
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.* Chem. Int. Ed. 2007, 46, 782.
Nickel-Catalyzed Coupling of Alkenes, Aldehydes, and Silyl Triflates. Ng, S.-S.; Ho, C.-Y.; Jamison, T. F.* Am. Chem. Soc. 2006, 128, 11513.
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.* Am. Chem. Soc. 2006, 128, 5326.
Fluorinated Chiral Secondary Amines as Catalysts for Epoxidation of Olefins with Oxone. Ho, C.-Y.; Chen, Y.-C.; Wong, M.-K.; Yang, D.* Org. Chem. 2005, 70, 898.
何振宇副教授
Email：jasonhcy@sustech.edu.cn
办公室：第一科研楼508
课题组主页：
http://faculty.sustech.edu.cn/jasonhcy/
何振宇博士于2000年-2005年在香港大学（the university of hong kong）化学系杨丹教授指导下从事有机不对称催化并获得博士学位，随后在麻省理工学院（M.I.T.） prof. timothy f. jamison研究组作为博士后从事过渡金属催化。从2007年底开始，在香港中文大学（the chinese university of hongkong）作为研究助理教授开始了独立的研究，从2013年起，加盟深圳南方科技大学(SUSTech)，入选深圳市孔雀计划b类人员，主要从事金属有机化学n-杂环卡宾及其在有机金属催化中的应用研究，在国内外学术刊物（angew. chem. int. ed, j. am.chem. soc，chem. commun., acs catal.等）发表论文多篇，并获the asian core program lectureship award (from japan)，the asian core program lectureship award (from singapore)等多项奖项。
教育背景：
2000.09-2005.07 —— 博士，香港大学，化学专业 (with Prof. D. Yang)
1997.09-2000.07 —— 学士，香港大学，化学专业
工作经历：
2013.01-至今 —— 副教授，南方科技大学，化学系
2007.09-2013.01 —— 研究助理教授，香港中文大学，化学系
2005.09-2007.07 —— 博士后，麻省理工学院，化学系 (with Prof. T. F. Jamison)
荣誉及奖励：
2017 —— Thieme化学期刊奖；有机化学研究员
2016 —— 深圳市南山区领航人才B类；南方科技大学优秀教学奖；南方科技大学青年教师教学竞赛奖
2015 —— 广东省本科高校化学类专业教学指导委员会委员
2013 —— 深圳市海外高层次人才B类；ACS Excellence in Science Symposium 最佳海报奖
2011 —— 亚洲核心计划讲学奖（新加坡）
2010 —— 亚洲核心计划讲学奖（日本）
2005-2007 —— 裘槎奖学金
新材料产业—先进石化工新材料—专用化学品及材料制造—专用化学品及材料制造
Diastereodivergent Hydrosilylative Enyne Cyclization Catalyzed by N-Heterocyclic Carbene-Ni(0) .Yu, M.; Yong, X.F.; Gao, W.W.; Ho, C.-Y. J. Chem. 2021, 39 , 1587.
NHC/Nickel(II)-Catalyzed [3+2] Cross-Dimerization of Unactivated Olefins and Methylenecyclopropanes. Huang, J.-Q.; Ho, C.-Y., Angewandte Chemie International Edition. 2020, 59 , 5288.
NHC-Ni catalyzed enantioselective synthesis of 1,4-dienes by cross-hydroalkenylation of cyclic 1,3-dienes and heterosubstituted terminal olefins. Chen, Y.; Dang, L.; Ho, C.-Y., Nature Communications. 2020, 11, 2269.
NHC-Ni catalyzed 1,3- and 1,4-diastereodivergent heterocycle synthesis from hetero-substituted enyne. Yong, X.; Gao, W.; Lin, X.; Ho, C.-Y., Communications 2020, 3, 50.
NHC-Ni(0) Catalyzed Diastereodivergent Hydroacylative Enyne Cyclization: Synthesis of Heterocycles bearing gamma-Enone. Advanced Synthesis & Catalysis. Yong, X.; Ng, E.; Zhen, Z.; Lin, X.; Gao, W.; Ho, C.-Y., 2020, 362 , 4164.
Applications of (NHC)Ni(II) Catalyzed [3+2] Hydroalkenylation-Rearrangement Cascades. Yong, X.; Huang, J.-Q., Ho, C.-Y., Chinese Journal of Organic Chemistry. 2020, 40 , 3327. (invited special issue: Prof. Henry N. C. Wong)
[(NHC)(NiH)-H-II]-Catalyzed Cross-Hydroalkenylation of Cyclopropenes with Alkynes: Cyclopentadiene Synthesis by [(NHC)Ni-II]-Assisted C-C Rearrangement. Huang, J.-Q.; Ho, C.-Y, Chem. Int. Ed. 2019, 58, 5702.
Electronic Effects on Chiral NHC–Transition-Metal. Yong, X., Thurston, R. & Ho, C.-Y,Synthesis 2019, 51, 2058.
Synthesis and Study of Au(III)-Indolizine Derivatives: Turn-on Luminescence by Photo-induced Control Release. Yang, J.; Zhu, Y.; Tse, A. K.-W.; Zhou, X.; Chen, Y.; Tse, Y. C.;* Wong, K. M.-C.;* Ho, C.-Y, Commun. 2019, 55, 4471.
(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, Chem. Int. Ed. 2018, 57, 2677.
(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.* Chem. Int. Ed. 2017, 56, 9048.
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.* Biomol. Chem. 2017, 15, 7131.
Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic Effects of Substrates and Chiral N-Heterocyclic Carbene Ligands Ho, C.-Y.*; Chan, C.-W.; He, L. Chem. Int. Ed. 2015, 54, 4512.
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.
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.
Nitrate-Enhanced NHC-NiH Catalyzed Tail-to-Tail Vinyl Ether Dimerization. He, L.; Ho, C.-Y.* 2014, 25, 2738.
Medium-Sized Heterocycle Synthesis by the Use of Synergistic Effects of Ni-NHC and γ‑Coordination in Cycloisomerization. Ho, C.-Y.*; He, L. J. Chem. 2014, 79, 11873.
Shuffle off the Classic -Si Elimination by Ni-NHC Cooperation: Implication for C-C Forming Reactions Involving Ni-Alkyl-β-Silanes. Ho, C.-Y.*; He, L. Commun. 2012, 48, 1481.
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. Chem. Int. Ed. 2010, 49, 9182.
Cyanative Alkene-Aldehyde Coupling: Ni(0)-NHC-Et2AlCN Mediated Chromanols Synthesis with High cis-Selectivity at room temperature. Ho, C.-Y.* Commun. 2010, 46, 466.
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.
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. Org. Chem. 2010, 8, 3480.
Alpha Olefins as Alkenylmetal Equivalents in Catalytic Conjugate Addition Reactions. Ho, C.-Y.; Ohmiya, H.; Jamison, T. F.* Chem. Int. Ed. 2008, 47, 1893.
Highly Chemoselective Reductive Amination of Carbonyl Compounds Promoted by InCl3/Et3SiH/MeOH System. Lee, O.-Y.; Law, K.-L.; Ho, C.-Y.; Yang, D.* Org. Chem. 2008, 73, 8829.
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.* Chem. Int. Ed. 2007, 46, 782.
Nickel-Catalyzed Coupling of Alkenes, Aldehydes, and Silyl Triflates. Ng, S.-S.; Ho, C.-Y.; Jamison, T. F.* Am. Chem. Soc. 2006, 128, 11513.
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.* Am. Chem. Soc. 2006, 128, 5326.
Fluorinated Chiral Secondary Amines as Catalysts for Epoxidation of Olefins with Oxone. Ho, C.-Y.; Chen, Y.-C.; Wong, M.-K.; Yang, D.* Org. Chem. 2005, 70, 898.
