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张勇健

 

 欢迎本科生、硕士生、博士生、博士后申请加入课题组。

 

1、基本信息
姓名:张勇健
职称:研究员
电话:021-54740787-13 
邮箱:yjian@sjtu.edu.cn
主页:scce.sjtu.edu.cn
通讯地址:上海市东川路800号上海交通大学电气绝缘楼312室

2、教育经历
1990-1994:延边大学化学系,学士
1994-1997:延边大学化学系,硕士
1999-2003:韩国科学技术研究院-韩国汉阳大学,博士
 

3、工作经历
1997-1999:延边大学化学系,助教

2003-2004:韩国科学技术研究院生命科学部,博士后
2009-2010:美国The University of Texas at Austin化学系,访问学者 

2004-至今:上海交通大学化学化工学院,副教授、研究员,博士生导师 


4、研究方向
1、绿色有机合成方法学
2、不对称催化
3、热熔粘接剂的开发及其制备工艺研究
4、阻燃剂的设计开发及其在高分子材料中的应用

5、科研项目
    主持和参加国家自然科学基金、973计划项目、上海市科委科技攻关项目、上海市浦江人才计划等多项课题研究。

6、荣誉奖励
1、2006:上海高校优秀青年教师科研基金, 上海市教委
2、2008:SMC优秀青年教师奖,上海交通大学
3、2011:上海市浦江人才计划,上海市人事局

4、2016: Thieme Chemistry Journals Award


7、教学工作
本科生:《有机化学》、《波谱分析》

8、代表性论文及专著
1.  Pd-Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Imines” Lei Yang, Ajmal Khan, Renfeng Zheng, Long Yi Jin, Yong Jian Zhang*, Org. Lett. 2015, 17, 6230.  (Highlighted in SYNFACTS 2016, 12, 273)

2. “Palladium-Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Electrophiles: Construction of Quaternary Stereocenters” Ajmal Khan, Yong Jian Zhang*, Synlett 2015, 26, 853.  (Invited Synpacts Article)

3. "Palladium-Catalyzed Enantioselective Decarboxylative Cycloaddition of Vinylethylene Carbonates with Isocyanates"  Ajmal Khan, Juxiang Xing, Jingming Zhao, Yuhe Kan, Wanbin Zhang, Yong Jian Zhang*, Chem. Eur. J. 2015, 21, 120.

4. "Palladium-Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Michael Acceptors: Construction of Vicinal Quaternary stereocenters" Ajmal Khan, Lei Yang, Jing Xu, Long Yi Jin, Yong Jian Zhang*Angew. Chem. Int Ed. 2014, 53, 11257. (Highlighted in SYNFACTS and ChemCatChem, 2015, 7, 51.) 

5. "Pd-Catalyzed Decarboxylative Cycloaddition of Vinylethylene Carbonates with Formaldehyde: Enantioselective Construction of Tertiary Vinylglycols” Ajmal Khan, Renfeng Zheng, Yuhe Kan, Jiang Ye, Juxiang Xing, Yong Jian Zhang*, Angew. Chem. Int. Ed. 2014, 53, 6439. (Highlighted in SYNFACT and ChemCatChem, 2015, 7, 51.) 

6. “Pd-Catalyzed Stereospecific Allyl-Aryl Coupling of Allylic Alcohols with Arylboronic Acids” Jiang Ye, Jingming Zhao, Jing Xu, Yuxue Mao, Yong Jian Zhang*, Chem. Commun. 2013, 49, 9761.

7. “Stereospecific Allyl–Aryl Coupling Catalyzed by in situ Generated Palladium Nanoparticles in Water under Ambient Conditions” Jingming Zhao, Jiang Ye, Yong Jian Zhang*, Adv. Synth. Catal. 2013, 355, 491. (Highlighted in SYNFACT ) 
8. “Pd-Catalyzed Regioselective and Stereospecific Suzuki-Miyaura Coupling of Allylic Carbonates with Arylboronic Acids” Chenguang Li, Juxiang Xing, Jingming Zhao, Patrick Huynh, Wanbin Zhang, Pingkai Jiang, Yong Jian Zhang*, Org. Lett. 2012, 14, 390.
 9. “Oligomeric Siloxane Containing Triphenylphosphonium Phosphate as a Novel Flame Retardant for Polycarbonate” Zongliu Tang, Yanan Li, Yong Jian Zhang*, Pingkai Jiang*, Polym. Degrad. Stabil. 2012, 97, 638. 
10. “Organocatalytic Enantioselective Michael-Addition of Malonic Acid Half-Thioester to β-Nitroolefins: From Mimicry of Polyketide Synthases to Scalable Synthesis of γ-Amino Acids” Han Yong Bae, Surajit Some, Jae Heon Lee, Joo Young Kim, Myoung Jong Song, Sungyul Lee*, Yong Jian Zhang*, Choong Eui Song*, Adv. Synth. Catal. 2011, 353, 3196.
11. “Iridium Catalyzed anti-Diastereo- and Enantioselective Carbonyl (α-Trifluoromethyl)allylation from the Alcohol or Aldehyde Oxidation Level” Xin Gao, Yong Jian Zhang, Michael J. Krische*, Angew. Chem. Int. Ed. 2011, 50, 4173
12. “anti-Diastereo- and Enantioselective Carbonyl (Hydroxymethyl)allylation from the Alcohol or Aldehyde Oxidation Level: Allyl Carbonates as Allylmetal Surrogates” Yong Jian Zhang, Jin Heak Yang, Sang Hoon Kim, Michael J. Krische*, J. Am. Chem. Soc. 2010, 132, 4502.
13. “Highly Efficient Asymmetric Organocatalytic Friedel-Crafts Alkylation of Indoles with a,ß-Unsaturated Aldehydes” Shangbin Jin, Chenguang Li, Yuanhui Ma, Yuhe Kan, Yong Jian Zhang*, Wanbin Zhang*, Org. Biomol. Chem. 2010, 8, 4011.
14. “Highly Active Asymmetric Diels-Alder Reactions Catalyzed by C2-Symmetric Bipyrrolidines: Catalyst Recycling in Water Medium and Insight into the Catalytic Mode” Yuanhui Ma, Shangbin Jin, Yuhe Kan, Yong Jian Zhang*, Wanbin Zhang*, Tetrahedron 2010, 66, 3849.
15. “Direct Prenylation of Aromatic and α,β-Unsaturated Carboxamides via Iridium-Catalyzed C-H Oxidative Addition-Allene Insertion” Yong Jian Zhang, Eduardas Skucas, Michael J. Krische*, Org. Lett. 2009, 11, 4248.
16. “C2-Symmetric Bipyrrolidines as Organocatalysts for Asymmetric Diels-Alder Reactions” Yuanhui Ma, Yong Jian Zhang*, Shangbin Jin, Qiqi Li, Chenguang Li, Junseong Lee, Wanbin Zhang*, Tetrahedron Lett. 2009, 50, 7388.
17. “Enantioselective Catalysis in Ionic Liquids and Supercritical CO2” Sang-gi Lee, Yong Jian Zhang, in Handbook of Asymmetric Heterogeneous Catalysis K. Ding, Y. Uozumi Ed. Wiley-VCH, Germany, 2008, 233-292.
18. “Chelation-Induced Axially Chiral Palladium Complex System with Tetraoxazoline Ligands for Highly Enantioselective Wacker-type Cyclization” Yong Jian Zhang, Feijun Wang, Wanbin Zhang*, J. Org. Chem. 2007, 72, 9208.
19. “Synthesis of Diastereomeric 1,4-Diphosphine Ligands Bearing Imidazolidin-2-one Backbone and Their Application in Rh(I)-Catalyzed Asymmetric Hydrogenation of Functionalized Olefins” Yong Jian Zhang, Kee Yong Kim, Jung Hwan Park, Choong Eui Song, Kyungae Lee, Myong Soo Lah, Sang-gi Lee*, Adv. Synth. Catal. 2005, 347, 563.
20. “Catalytic Asymmetric Hydrogenation in a Room Temperature Ionic Liquid Using Chiral Rh-complex of Ionic Liquid Grafted 1,4-Bisphosphine Ligand” Sang-gi Lee*, Yong Jian Zhang, Jing Yu Piao, Hyeon Yoon, Choong Eui Song, Jung Hoon Choi, Jongki Hong, Chem. Commun. 2003, 2624.
21. “Rh(I)-Catalyzed Enantioselective Hydrogenation of (E)- and (Z)-β-(Acylamino)acrylates Using 1,4-Bisphosphine Ligands under Mild Conditions” Sang-gi Lee*, Yong Jian Zhang, Org. Lett. 2002, 4, 2429.
22. “Novel 1,4-Diphosphanes with Imidazolidin-2-one Backbones as Chiral Ligands: Highly Enantioselective Rh-Catalyzed Hydrogenation of Enamides” Sang-gi Lee*, Yong Jian Zhang, Choong Eui Song, Jae Kyun Lee, Jung Hoon Choi, Angew. Chem. Int. Ed. 2002, 41, 847.



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