Следене
shengtao ding
shengtao ding
Потвърден имейл адрес: mail.buct.edu.cn
Заглавие
Позовавания
Позовавания
Година
N,N‐Dimethylformamide: A Multipurpose Building Block
S Ding, N Jiao
Angewandte Chemie International Edition 51 (37), 9226-9237, 2012
4432012
Indoles from Simple Anilines and Alkynes: Palladium‐Catalyzed C H Activation Using Dioxygen as the Oxidant
Z Shi, C Zhang, S Li, D Pan, S Ding, Y Cui, N Jiao
Angewandte Chemie 121 (25), 4642-4646, 2009
4272009
Direct Transformation of N,N-Dimethylformamide to −CN: Pd-Catalyzed Cyanation of Heteroarenes via C–H Functionalization
S Ding, N Jiao
Journal of the American Chemical Society 133 (32), 12374-12377, 2011
3122011
Iridium‐Catalyzed Intermolecular Azide–Alkyne Cycloaddition of Internal Thioalkynes under Mild Conditions
S Ding, G Jia, J Sun
Angewandte Chemie 126 (7), 1908-1911, 2014
3042014
A palladium‐catalyzed oxidative cycloaromatization of biaryls with alkynes using molecular oxygen as the oxidant
Z Shi, S Ding, Y Cui, N Jiao
Angewandte Chemie International Edition 48 (42), 7895-7898, 2009
2522009
Ligand-controlled remarkable regio-and stereodivergence in intermolecular hydrosilylation of internal alkynes: experimental and theoretical studies
S Ding, LJ Song, LW Chung, X Zhang, J Sun, YD Wu
Journal of the American Chemical Society 135 (37), 13835-13842, 2013
1472013
Pd (II)-Catalyzed synthesis of carbolines by iminoannulation of internal alkynes via Direct C− H bond cleavage using dioxygen as oxidant
S Ding, Z Shi, N Jiao
Organic Letters 12 (7), 1540-1543, 2010
1472010
Copper-catalyzed direct oxidative annulation of N-iminopyridinium ylides with terminal alkynes using O 2 as oxidant
S Ding, Y Yan, N Jiao
Chemical Communications 49 (39), 4250-4252, 2013
1032013
Highly regio‐and stereoselective hydrosilylation of internal thioalkynes under mild conditions
S Ding, LJ Song, Y Wang, X Zhang, LW Chung, YD Wu, J Sun
Angewandte Chemie International Edition 54 (19), 5632-5635, 2015
942015
An efficient difluorohydroxylation of indoles using Selectfluor as a fluorinating reagent
R Lin, S Ding, Z Shi, N Jiao
Organic Letters 13 (17), 4498-4501, 2011
802011
Ir-catalyzed regio-and stereoselective hydrosilylation of internal thioalkynes: a combined experimental and computational study
LJ Song, S Ding, Y Wang, X Zhang, YD Wu, J Sun
The Journal of Organic Chemistry 81 (15), 6157-6164, 2016
482016
Ru-catalyzed migratory geminal semihydrogenation of internal alkynes to terminal olefins
L Song, Q Feng, Y Wang, S Ding, YD Wu, X Zhang, LW Chung, J Sun
Journal of the American Chemical Society 141 (43), 17441-17451, 2019
452019
Iridium-catalyzed hydrosilylation of unactivated alkenes: scope and application to late-stage functionalization
X Xie, X Zhang, H Yang, X Ji, J Li, S Ding
The Journal of Organic Chemistry 84 (2), 1085-1093, 2018
412018
1, 2, 3-Triazole-based sequence-defined oligomers and polymers
X Wang, X Zhang, S Ding
Polymer Chemistry 12 (18), 2668-2688, 2021
392021
Transition Metal‐Catalyzed Cycloaddition of Azides with Internal Alkynes
J Ma, S Ding
Asian Journal of Organic Chemistry 9 (12), 1872-1888, 2020
362020
Investigations on Gold‐Catalyzed Thioalkyne Activation Toward Facile Synthesis of Ketene Dithioacetals
X Ye, J Wang, S Ding, S Hosseyni, L Wojtas, NG Akhmedov, X Shi
Chemistry–A European Journal 23 (44), 10506-10510, 2017
362017
Synthesis of functionalized pyrazolo [1, 5-a] pyridines:[3+ 2] cycloaddition of N-aminopyridines and α, β-unsaturated carbonyl compounds/alkenes at room temperature
C Ravi, S Samanta, DC Mohan, NNK Reddy, S Adimurthy
Synthesis 49 (11), 2513-2522, 2017
362017
Iridium-catalyzed Markovnikov hydrosilylation of terminal alkynes achieved by using a trimethylsilyl-protected trihydroxysilane
X Xie, X Zhang, W Gao, C Meng, X Wang, S Ding
Communications Chemistry 2 (1), 101, 2019
332019
Phosphane‐Free Copper‐Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Halides under Aerobic Conditions
D Pan, C Zhang, S Ding, N Jiao
European journal of organic chemistry 2011 (25), 4751-4755, 2011
332011
Efficient synthesis of diverse 5-thio-or 5-selenotriazoles: one-pot multicomponent reaction from elemental sulfur or selenium
LL Zhang, YT Li, T Gao, SS Guo, B Yang, ZH Meng, QP Dai, ZB Xu, ...
Synthesis 51 (22), 4170-4182, 2019
312019
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