arylation论文范文

Zhu, L., Chen, H., Meng, Q., Fan, W., Xie, X., Zhang, Z., Highly enantioselective hydrogenation of 2-oxo-4-arybutanoic acids to 2-hydroxy-4-arylbutanoic acids. Tetrahedron 2011, 67 (34), 6186-6190. Yao, Y., Fan, W., Li, W., Ma, X., Zhu, L., Xie, X., Zhang, Z., Synthesis of (S)-7-amino-5-azaspiro[]heptane via highly enantioselective hydrogenation of protected ethyl 1-(2-aminoaceto)cyclopropanecarboxylates. J. Org. Chem. 2011, 76 (8), , Y., Chen, L., Zhang, Z., Zhang, Y., Palladium-catalyzed oxidative C-H bond and C=C double bond cleavage: C-3 acylation of indolizines with α,β-unsaturated carboxylic acids. Organic Letters 2011, 13 (6), , X., Ni, G., Ma, F., Ding, L., Xu, S., Zhang, Z., Palladium-catalyzed monoarylation of aryl amine with aryl tosylates. Synlett 2011, (7), , F. F., Peng, Z. Y., Li, W. F., Xie, X. M.,Zhang, Z., An efficient Pd-catalyzed coupling of hydrazine derivatives with aryl halides. Synlett 2011, (17), , F., Xie, X., Ding, L., Gao, J., Zhang, Z., Palladium-catalyzed coupling reaction of amino acids (esters) with aryl bromides and chlorides. Tetrahedron 2011, 67 (48), , X., Ma, X., Li, W., Tao, X., Meng, Q., Fan, W., Zhang, Z., Catalytic asymmetric hydrogenation of ethyl 2-(benzo[b]thiophen-5-yl)-2- oxoacetate with ru-sunphos in the formal synthesis of T-588. Chinese Journal of Chemistry 2011, 29 (12), , W., Ma, X., Fan, W., Tao, X., Li, X., Xie, X., Zhang, Z., Ru-catalyzed asymmetric hydrogenation of 3-oxoglutaric acid derivatives via solvent-assisted pinpoint recognition of carbonyls in close chemical propinquity. Organic Letters 2011, 13 (15), , W., Li, W., Ma, X., Tao, X., Li, X., Yao, Y., Xie, X., Zhang, Z., Ru-catalyzed asymmetric hydrogenation of γ-heteroatom substituted β-keto esters. J. Org. Chem. 2011, 76 (22), , L., Meng, Q., Fan, W., Xie, X., Zhang, Z., Direct asymmetric hydrogenation of 2-oxo-4-arylbut-3-enoic acids. J. Org. Chem. 2010, 75 (17), , X., Ding, L., Ni, G., Zhang, Z., Gao, J., A general and facile approach for the synthesis of 2'-functionalized 1,1'-binapthyl-2-ols. Chinese Journal of Chemistry 2010, 28 (9), , J., Tong, X., Xie, X., Zhang, Z., Rhodium-catalyzed activation of C(sp3)-X (X = Cl, Br) bond: An intermolecular halogen exchange case. Organic Letters 2010, 12 (23), , Z. Y., Ma, F. F., Zhu, L. F., Xie, X. M., Zhang, Z., Lewis acid promoted carbon - Carbon double-bond formation via organozinc reagents and carbonyl compounds. J. Org. Chem. 2009, 74 (17), , X., Busch-Petersen, J., Deng, J., Edwards, C., Zhang, Z., Kerns, J. K., Efficient and scalable synthesis of 3,5,7-trisubstituted 1H-indazoles as potent IKK2 inhibitors. Synlett 2008, (20), 3216-3220. Xie, X., Zhang, T. Y., Zhang, Z., Synthesis of bulky and electron-rich MOP-type ligands and their applications in palladium-catalyzed C-N bond formation. J. Org. Chem. 2006, 71 (17), , L., Chen, H., Meng, Q., Fan, W., Xie, X., Zhang, Z., Highly enantioselective hydrogenation of 2-oxo-4-arybutanoic acids to 2-hydroxy-4-arylbutanoic acids. Tetrahedron 2011, 67 (34), , Y., Fan, W., Li, W., Ma, X., Zhu, L., Xie, X., Zhang, Z., Synthesis of (S)-7-amino-5-azaspiro[]heptane via highly enantioselective hydrogenation of protected ethyl 1-(2-aminoaceto)cyclopropanecarboxylates. J. Org. Chem. 2011, 76 (8), , X., Zhang, T. Y., Zhang, Z., Synthesis of bulky and electron-rich MOP-type ligands and their applications in palladium-catalyzed C-N bond formation. J. Org. Chem. 2006, 71 (17), , D.; Zhang, Z. “Activation and reaction of carboxylic anhydride catalyzed by palladium ” Chin. J. Org. , 24, , M.; Li, D.; Sun, Y.; Zhang, Z. “Selective Reduction of the Carbonyl Group in b,g-Unsaturated a-Ketoesters by Transfer Hydrogenation with Ru-TsDPEN” Synlett, 2004, 741-743Luo, Y.; Wang, F.; Zhu, G.; Zhang, Z. “A concise synthesis of 2-diarylphosphino-20-methoxy-1,10-binaphthalenes (MOPs) by simple resolution”, Tetrahedron Asymm. 2004, 15, , M.; Li, D.; Zhang, Z. “Novel Synthesis of 2-Oxo-3-butynoates by Copper-Catalyzed Cross-Coupling Reaction of Terminal Alkynes and Monooxalyl Chloride”, J. Org. Chem. 2003, 68, , D.; Zhang, Z. “Palladium-Catalyzed Cross-Coupling Reactions of Carboxylic Anhydrides with Organozinc Reagents”, Org. Lett., 2003, 5, , G.; Zhang, Z. “Palladium-Catalyzed Tandem Cyclization/Suzuki Coupling of 1,6-Enynes”, Org. Lett., 2003, 5, , J.; Wang, F.; Xu, .; Pan, Y.; Zhang, Z. “Palladium-catalyzed Suzuki–Miyaura reaction using aminophosphine as ligand”, Tetrahedron Lett., 2003, 44, , X., Zhang, Z., Zhang, X., “Novel Rhodium-Catalyzed Cycloisomerization of 1,6-Enynes with an Intramolecular Halogen Shift” J. Am. Chem. Soc. 2003, 125, , Z.; Lu, X*. and Lang, S. “An Unexpected Reaction of Allyl Propynoate under Palladium Catalysis” Chin. J. Chem. 2002, 20, , F. and Zhang Z.* “Palladium Catalyzed Amidocarbonylation”, Chin. J. Org. Chem. 2002, 22, , J. Z.; Zhang, Z. G.; Yang, X. L.; Fun, K. H. and Xu*, J. H “Photooxygenation of Indolizines via Selective Excitation of Their Charge Transfer Complexes with Molecular Oxygen” J. Org. Chem. 2001, 66, 8230-8235Zhang,Z.; Lu, X.*; Xu, Z.; Zhang, Q. and Han, X. “Role of Halide Ions in Divalent Palladium-Mediated Reactions: Competition between ‚-Heteroatom Elimination and ‚-Hydride Elimination of a Carbon-Palladium Bond”, Organometallics 2001, 20, 3724-3728Zhang, Z.; Qian, H.; Longmire, J. and Zhang, X*. “Synthesis of Chiral Bisphosphines with Tunable Bite Angles and Their Applications in Asymmetric Hydrogenation of –Ketoesters”, J. Org. Chem. 2000; 65; , W.; Zhang, Z.; Xiao, D. and Zhang, X*. “Synthesis of Chiral hydroxl Phosphines from D-Mannitol and Their Use in Asymmetric Catalytic Reactions” J. Org. Chem., 2000, 65, , Z.; Zhang, Z.; Lu, X*. “Effect of Halide Ligands on the Reactivity of Carbon-Palladium Bonds: Implications for Designing Catalytic Reactions” Organometallics, 2000, 19, , W.; Zhang, Z.; Xiao, D.; Zhang, X*. “Rhodium-hydroxyl bisphospholane catalyzed highly enantioselective hydrogenation of dehydroamino acids and esters” Tetrahedron Lett., 1999, 40, , Q.; Xiao, D.; Zhang, Z.; Cao, P.; Zhang, X*. “Highly enantioselective hydrogenation of cyclic enol acetates catalyzed by a Rh-PennPhos complex” Angew. Chem., Int. Ed., 1999, 38, , Z.; Zhu, G.; Jiang, Q.; Xiao, D.; Zhang, X*. Highly Enantioselective Hydrogenation of Cyclic Enamides Catalyzed by a Rh-PennPhos Catalyst” J. Org. Chem., 1999, 64, , D.; Zhang, Z.; Zhang, X*. “Synthesis of a Novel Chiral Binaphthyl Phospholane and Its Application in the Highly Enantioselective Hydrogenation of Enamides” Org. Lett., 1999, 1, , D.; Zhang, Z.; Jiang, Q.; Zhang, X.. “Syntheses of novel chiral 2,5-dialkyl-7- azabicyclo[]heptanes and 2,5-dialkyl-7-thiobicyclo[]heptanes” Tetrahedron Lett., 1998, 39, , Z.; Lu, X*.; Lei, A.; Zhang, Z. “Efficient Preparation of Functionalized (E,Z) Dienes Using Acetylene as the Building Block” J. Org. Chem., 1998, 63, , X*.; Zhu, G.; Wang, Z.; Ma, S.; Ji, J.; Zhang, Z. “Enyne cyclization methodology for the synthesis of bioactive lactones” Pure Appl. Chem., 1997, 69, , X.; Zhu, G.; Wang, Z.; Ma, S.; Ji, J.; Zhang, Z. “Enyne cyclization methodology for the synthesis of bioactive lactones” Youji Huaxue, 1997. 17, , Z.; Lu, X*. “Total synthesis of phaseolinic acid by enyne cyclization” Tetrahedron: Asymm. 1996, 7, , J.; Song, Y.; Zhang, Z.; Wang, L.; Xu, J*. “Photoinduced addition reactions of chloranil with alkenes - factors influencing the reaction site” Tetrahedron, 1994, 50, , C.; Zhang,Z.; Yan, B.; Xu, J*. “Phtoinduced Reactions of Chloranil with Aromatic Imines” Tetrahedron Lett. 1994, 35, , B.; Zhang, Z.; Yuan, H.; Wang, L. and Xu, J*. “Photoinduced Electron- transfer Reactions of Chloranil with Benzodioxoles” J. Chem. Soc. Perk. T 2, 1994, 2545-2550.

绍兴文理学院正式更名绍兴大学。

绍兴文理学院是一所由绍兴市举办的地方应用型普通本科高校，绍兴人文荟萃、文化灿烂，可是，在高等教育方面，绍兴非常落后。

截至目前，绍兴还没有高水平大学（高水平大学指具有博士授权的大学），杭州电子科技大学绍兴校区还没有建好，所以，绍兴文理学院已经是绍兴市非常好的高校了，作为绍兴地区高等教育的领头羊，绍兴市非常关注和支持绍兴文理学院的发展。

绍兴文理学院在2013年正式拿到硕士学位授权资格，学科建设正式起步，该校现有“工程学”一个学科进入Esi排名前1%，对于一所应用型地方本科高校来说，这是一件非常不容易的事情！不仅如此，该校研究生占比已经满足了教育部规定的5%指标，甚至大大超过了这个指标。

在同类高校中，绍兴文理学院的综合水平是比较强的了，如此强大的实力也让该校在科研领域内硕果累累！

（注：所谓同类型高校中，指的是应用型本科高校，比如浙江科技学院、宁波财经学院、浙大城市学院、宁波工程学院、温州理工学院等等）。

近日，绍兴文理学院教师在Nature Index期刊《Organic Letters》上发表了自己的研究论文，这篇文章的英文全名是“Visible-Light-Induced α-Amino C–H Bond Arylation Enabled by Electron Donor–Acceptor Complexes”，这是一篇化学领域内的学术文章，由绍兴文理学院化学化工学院冯高峰课题组产出。

这篇文章的含金量还是非常高的，虽然不能与国际顶级期刊相比，但是，对于绍兴文理学院来说，这也是一次科研之旅，体现了该校孜孜不倦的科研追求。

强大的科研水平是更名“绍兴大学”的必要条件，绍兴文理学院已经满足了更名大学的各种条件，该校正在等待教育部专家组进校考核，后期的程序还有专家组投票、教育部整理公示，一般来说，公示期需要半个月，公示期结束之后，如果社会无异议，教育部则会正式通知更名成功。