86. Ying-Chun Song , Wen-Hui Cao , Ming-Xuan Wang, Run-Qing Wang, Yuan-Yuan Sun, An-Xin Wu*, Yan-Ping Zhu*. One-Pot Total Synthesis of Natural Products Nitramarine, Nitraridine, and Analogues via a Cascade Oxidation/Pictet–Spengler Condensation/Annulation Process.
J. Org. Chem. 2024, 89, 12832–12841 DOI: 10.1021/acs.joc.4c01441. https://pubs.acs.org/doi/full/10.1021/acs.joc.4c01441
85. Hang Liu, Yi-Xin Chai, Jun-Jie Yang, Dan Miao, Meng-Yao Wang, Ting Jiang, Yuan-Yuan Sun, Xin Lu, Qing Sun*, Jin-Heng Li*, and Yan-Ping Zhu*. Palladium/Norbornene Cooperative Catalysis Bifunctionalization: Acylation/Cyanation of Aryl Iodides by Cleaving C–CN Bond of Aryl Acyl Nitrile.
Highlight by CGB咨讯: 烟台大学祝艳平课题组Org. Lett.
Adv. Synth. Catal. 2024, 366, 1348-1355, DOI: 10.1002/adsc.202301322. https://doi.org/10.1002/adsc.202301322
Chinese Chemical Letters 2024, 109685. DOI: 10.1016/j.cclet.2024.109685. https://doi.org/10.1016/j.cclet.2024.109685
80. Fu-Rao Liu , Jun-Jie Ren , Meng-Yao Wang , Hao-Yu Liu , Jian-Kang Cao , Yu Ding , Zi-Han Xue , Xin-Shuang Zhang, Yan-Ping Zhu*, Yuan-Yuan Sun*. Ru(II)-catalyzed cyclization of 1-aryl-5-aminopyrazoles and α-diazolidinones for one-pot synthesis of benzopyrazole[1,3]diazepines in H2O/EtOH.
Tetrahedron 2024, 160, 134047, DOI: 10.1016/j.tet.2024.134047. https://doi.org/10.1016/j.tet.2024.134047
79. Jian-Kang Cao, Tian-Zheng Cao, Qian-Wen Yue, Ying Ma, Chuan-Ming Yang, Hong-Xi Zhang, Ya-Chen Li, Qiao-Ke Dong, Yan-Ping Zhu* and Yuan-Yuan Sun*. tert-Butyl Nitrite-Induced Radical Nitrile Oxidation Cycloaddition: Synthesis of Isoxazole/Isoxazoline-Fused Benzo 6/7/8-membered Oxacyclic Ketones.
Molecules 2024, 29, 1202, DOI: 10.3390/molecules29061202. https://doi.org/10.3390/molecules29061202
78. Yumei Wang, Guangzhu Wang, Yanping Zhu*, Kaiwu Dong*. Chiral phosphoric acid-catalyzed transfer hydrogenation of 3,3-difluoro-3H-indoles.
77. Wenjuan Li, Chaoren Shen, Yanping Zhu*, Kaiwu Dong*, Practical Fischer Indolization Using Bench-Stable Arylhydrazine Sulfonate as the Surrogate of Arylhydrazine.
Synlett. 2024, 35, 1165-1169. DOI: 10.1055/s-0043-1763622. https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-1763622
76. Jun-Jie Ren, Jia-Xin Zhou, Yanqin Song, An-Xin Zhang, Lu-Xin Zhao, Zun-Yuan Zhao, Yan-Ping Zhu*, Wei Zhu* Cascade Wolff rearrangement and double N-acylation: a cyclization of α-diazoketones with 2-aminopyridines or 3-aminopyrazoles to synthesize fused pyrimidinedione.
Adv. Synth. Catal. 2023, 23, 4121-4126. DOI: 10.1002/adsc.202300773. https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.202300773
Cover paper: https://onlinelibrary.wiley.com/doi/10.1002/adsc.202301269
75. Zhuo Wang, Yu-Han Zhao, Jia-Xin Chen, Meng-Yao Chen, Xue-Han Li, Ting Jiang, Fang Liu, Xi Yang, Yuan-Yuan Sun, Yan-Ping Zhu*. One-Pot Synthesis of Isoxazole-Fused Tricyclic Quinazoline Alkaloid Derivatives via Intramolecular Cycloaddition of Propargyl-Substituted Methyl Azaarenes under Metal-Free Conditions.
Molecules. 2023, 28, 2787. DOI: 10.3390/molecules28062787. https://doi.org/10.3390/molecules28062787.
74. Yan-Ping Zhu*, Yu Zhou, Wen-Juan Li, Fu-Rao Liu, Wen-Cheng Wang, Kai-Yan Hao, Bing-Yu Chao, Tian-Ru Shi, An-Xin Wu, Yuan-Yuan Sun, Iodine-Promoted Oxidative Cyclization of Methyl Azaarenes and α-Amino Ketones for One-Pot Synthesis of 2-Azaaryl-5-aryl Oxazoles.
J. Org. Chem. 2022, 87, 12460–12469. DOI: 10.1021/acs.joc.2c01399. https://doi.org/10.1021/acs.joc.2c01399
73. Xiao-Yu Miao, Yong-Ji Hu, Fu-Rao Liu, Yuan-Yuan Sun, Die Sun, An-Xin Wu* and Yan-Ping Zhu*. Synthesis of Diversified Pyrazolo[3,4-b]pyridine Frameworks from 5-Aminopyrazoles and Alkynyl Aldehydes via Switchable C≡C Bond Activation Approaches.
Molecules. 2022, 27, 6381. DOI: 10.3390/molecules27196381. https://doi.org/10.3390/molecules27196381.
(Invited Paper for the Special Issue Catalysis for Green Chemistry)
72. Yong-Ji Hu,† Yu Zhou,† Jing-Jing Gao,†Han Zhang,† Kai-Rui Yang, Jia-Jun Li, Xiao-Xin Yan, Yuan-Lin Li, Yan-Ping Zhu*, I2-Mediated [3 + 2] annulation of methyl-azaarenes with alkyl 2-isocyanoacetates or amino acid ester hydrochlorides: selective synthesis of iodine-functionalized and non-iodine-functionalized fused imidazoles.
Organic Chemistry Frontiers, 2022, 9, 1403-1409. DOI: 10.1039/D1QO01940F. https://doi.org/10.1039/D1QO01940F
71. Xiang-Jin Zhang,† Jian-Kang Cao,† Jun-Jie Ren, Lin Hong, Ru-Jin Liang, Kai-Yan Hao, Kai-Li Wei, Bao-Jing Mi, Yue Liu, Yan-Ping Zhu*, Generation of azaarene nitrile oxides from methyl azaarenes and t-BuONO enabling synthesis of furoxans and 1,2,4-oxadiazoles.
Organic Chemistry Frontiers, 2022, 9, 1121-1126. DOI: 10.1039/D1QO01872H. https://doi.org/10.1039/D1QO01872H
highlight by: Frontiers Journals https://mp.weixin.qq.com/s/NsUC_rVwBby4fRWilPKlbw
70. Xiao-Dong Liu, Qiu-An Wang, Yan-Ping Zhu,* Zhi-Hong Peng*, Jin-Heng Li*, Copper-catalyzed aerobic hydroxyamination of alkenes of unsaturated keto oximes in EtOH toward cyclic nitrones.
Green Chem., 2022, 24, 2476-2482. DOI: 10.1039/D2GC00017B. https://doi.org/10.1039/D2GC00017B
69. Xin-Ke Zhang,† Xiao-Yu Miao,† Yu Zhou,† Yu-Mei Wang, Ying-Chun Song, Hang Liu, Yi-Lu Xiong, Ling-Yu Li, An-Xin Wu, Yan-Ping Zhu*, Iodine-Catalyzed Oxidative Annulation: Facile Synthesis of Pyrazolooxepanopyrazolones via Methyl azaarenes sp3 C-H Functionalization.
Organic & Biomolecular Chemistry, 2022, 20, 1236-1242. DOI: 10.1039/D1OB02436A. https://doi.org/10.1039/D1OB02436A
68. Xiang-Jin Zhang,† Zhuo Wang,† Han Zhang,† Jing-Jing Gao,† Kai-Rui Yang, Wei-Yu Fan, Rui-Xue Wu, Meng-Lin Feng, Wei Zhu, Yan-Ping Zhu*, Iodine-Mediated Domino Cyclization for One-Pot Synthesis of Indolizine-Fused Chromones via Metal-Free sp3 C-H Functionalization
J. Org. Chem. 2022, 87, 835–845, DOI: 10.1021/acs.joc.1c02508. https://doi.org/10.1021/acs.joc.1c02508
67. Chong-Hui Xu, Zhi-Qiang Xiong, Yang Li, Yan-Ping Zhu*, Jin-Heng Li*, Copper-catalyzed oxidative phosphonoheteroarylation of alkenes with phosphonates and N-heteroarenes via P–H/C–H functionalization.
Org. Chem. Front. 2022, 9, 476-480. DOI: 10.1039/D1QO01644J. https://pubs.rsc.org/en/content/articlelanding/2022/QO/D1QO01644J
Org. Lett.2021, 23, 9543–9547, DOI: 10.1021/acs.orglett.1c03762. https://pubs.acs.org/doi/10.1021/acs.orglett.1c03762
65. Xiang-Jin Zhang, Jie Zhang, Yu-Ning Xu, Yi-Ming Li, Man Chi, Yu Yan, Rui-Xue Wu, Hui-Ru Zhang, Yan-Ping Zhu* , Cascade Wolff Rearrangement/Acylation: A Metal-Free and Eco-Friendly Approach for 4-Hydroxy-pyrazolo[3,4-b]pyridin-6-ones and N-Pyrazole Amides Synthesis from 5-Aminopyrazoles and α-Diazoketones.
J. Org. Chem. 2021, 86, 17471–17481. DOI: 10.1021/acs.joc.1c02165. https://doi.org/10.1021/acs.joc.1c02165
Highlight by：（1）Organic Chemistry Portal: https://www.organic-chemistry.org/Highlights/2022/26September.shtm
（2）Synfacts 2022; 18(03): 0254，DOI: 10.1055/s-0041-1737883，
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0041-1737883
64. Qi-Qi Hu, Yan-Ting Gao, Jia-Chen Sun, Jing-Jing Gao, Hong-Xiao Mu, Yi-Ming Li, Ya-Nan Zheng, Kai-Rui Yang, Yan-Ping Zhu*, Iodine-imine Synergistic Promoted Povarov-Type Multicomponent Reaction for the Synthesis of 2,2′-Biquinolines and Their Application to a Copper/Ligand Catalytic System.
Org. Lett. 2021, 23, 9000–9005. DOI: 10.1021/acs.orglett.1c03546. https://doi.org/10.1021/acs.orglett.1c03546
Highlight by: CBG资讯 https://mp.weixin.qq.com/s/NJtYxi3_x98EiqEdXlO4RA
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63. M.-J. Luo, X.-H. Ouyang, Y.-P. Zhu,* Y. Li*, J.-H. Li*, Metal-free electrochemical [3 + 2] heteroannulation of anilines with pyridines enabled by dual C–H radical aminations.
Green Chem., 2021, 23, 9024-9029. DOI: 10.1039/D1GC02922C. https://doi.org/10.1039/D1GC02922C
62. Zhi-Hao Shang,+ Xiang-Jin Zhang,+ Yi-Ming Li,+ Rui-Xue Wu,+ Hui-Ru Zhang, Lu-Ying Qin, Xue Ni, Yu Yan, An-Xin Wu*, Yan-Ping Zhu*, One-Pot Synthesis of Chromone-Fused Pyrrolo[2,1-a]isoquinolines and Indolizino[8,7-b]indoles: Iodine-Promoted Oxidative [2 + 2 + 1] Annulation of O-Acetylphenoxyacrylates with Tetrahydroisoquinolines and Noreleagnines.
J. Org. Chem. 2021, 86, 15733–15742. https://doi.org/10.1021/acs.joc.1c01682
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https://mp.weixin.qq.com/s/RXDNY2Mj7lN9E8Ox38TxzA
61. Xin-Ke Zhang,Xiao-Yu Miao,Hui-Ru Jiang, Fei Ge, Jia-Chen Sun, Rui-Ying Zhang, Qin Ouyang, Wei-Yu Fan, Yan-Ping Zhu*,Yuan-Yuan Sun*, Iodine-Promoted Synthesis of Dipyrazolo/Diuracil-Fused Pyridines and o-Amino Diheteroaryl ketones via Oxidative Domino Annulation of 2/4-Methylazaarenes.
Adv. Synth. Catal. 2021, 363, 4632-4638. DOI: 10.1002/adsc.202100839. https://doi.org/10.1002/adsc.202100839
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60. J. Chen, Y.-P. Zhu*, J.-H. Li*, Q.-A. Wang*, External-oxidant-free amino-benzoyloxylation of unactivated alkenes of unsaturated ketoximes with O-benzoylhydroxylamines.
Chem. Commun., 2021, 57, 5215-5218. DOI: 10.1039/D1CC01565F. https://doi.org/10.1039/D1CC01565F
59. Ziyong Li*, Haining Zhang, Xiaoxiao Hu, Huijuan Zhu, Limin Shen, Congmin Liu, Xiaoman Zhang, Xinyu Gao, Lingmei Li, Yan-Ping Zhu*, Frontiers in Chemistry, 2021, 9, 665880. DOI: 10.3389/fchem.2021.665880.
https://www.frontiersin.org/articles/10.3389/fchem.2021.665880/abstract
58. J. Chen, J.-H. Li*, Y.-P. Zhu*, Q. Wang*, Copper-catalyzed enantioselective arylboronation of activated alkenes leading to chiral 3,3′-disubstituted oxindoles.
Organic Chemistry Frontiers, 2021, 8, 2532-2536. DOI: 10.1039/D1QO00186H. https://doi.org/10.1039/D1QO00186H
57. Rong-Ji Xie#, Jun-Hua Liu#, Qiu-Yi Zhang#, Yi-Jie Yang#, Li-Qun Song, Tian-Qi Shao, Kai-Xuan Liu, Yan-Ping Zhu*，Copper-catalyzed aerobic oxidative domino cyclization of methyl azaarenes with 6-amino-pyrimidine-2,4-diones and pyrazol-5-amines: access to dipyrimidine/dipyrazolo-fused pyridines.
Organic Chemistry Frontiers, 2021, 8, 2274-2279. DOI: 10.1039/D0QO01588A. https://doi.org/10.1039/D0QO01588A
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56. Fei-Fei Liang, Kai-Xuan Liu, Cong Zhao, Zhi-Hao Shang, Hong-Mei Kong, Ya-Qing Yin, Yan-Ping Zhu*, Yuan-Yuan Sun*, Jian-Wen Yao*. Eur. J. Org. Chem. 2021, 6, 998-1002. DOI: 10.1002/ejoc.202001561 (VIP paper)
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202001561
Highlight by WileyChem: https://mp.weixin.qq.com/s/KBqdXI6nI3gSJm4XyYx0fw
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55. Zhi-Hao Shang, Zhen-Xiao Zhang, Wei-Zhao Weng, Yu-Fei Wang, Tian-Wei Cheng, Qiu-Yi Zhang , Li-Qun Song, Tian-Qi Shao, Kai-Xuan Liu, Yan-ping Zhu*, A Metal- and Azide-free Oxidative Coupling Reaction for the Synthesis of [1,2,3]Triazolo[1,5-a]quinolines and their Application to Construct C−C and C-P Bonds, 2-Cyclopropylquinolines and Imidazo[1,5-a]quinolines.
Adv. Synth. Catal. . 2021, 363, 490-496. DOI:10.1002/adsc.202001052, https://onlinelibrary.wiley.com/doi/10.1002/adsc.202001052
54. Peng Zhao, Xiao-Xiao Yu, You Zhou, Xiao Geng, Can Wang, Chun Huang, Yan-Dong Wu, Yan-Ping Zhu,* and An-Xin Wu*, Splitting Methyl Ketones into Two Parts: Synthesis of 4(3H)‑Quinazolinones via Consecutive Cyclization/Ring-Opening Reaction.
Org. Lett. 2020, 22, 7103–7107. DOI: 10.1021/acs.orglett.0c02415, https://doi.org/10.1021/acs.orglett.0c02415
53. Peng Zhao, Xiao-Xiao Yu, You Zhou, Chun Huang, Yan-Dong Wu, Yan-Ping Zhu*, An-Xin Wu*, Arylacetylenes as two-carbon synthons: synthesis of eight-membered rings via CC bond cleavage.
Chem. Commun. 2020, 56, 12554-12557. DOI：10.1039/D0CC05363E, https://doi.org/10.1039/D0CC05363E
52. Leiling Deng, Yunyun Liu, Yanping Zhu*, Jie-Ping Wan*, Transition‐Metal‐Free Annulation of Enamines and Tosyl Azide toward N-Heterocycle Fused and 5-Amino-1,2,3-Triazoles.
Eur. J. Org. Chem. 2020, 34, 5606-5609. DOI: 10.1002/ejoc.202000938
https://doi.org/10.1002/ejoc.202000938
51. Shanghui Tian, Tian Luo, Yanping Zhu*, Jie-Ping Wan*, Recent advances in the diversification of chromones and flavones by direct C-H bond activation or functionalization.
Chinese Chemical Letters, 2020, 31, 3073-3082, DOI: 10.1016/j.cclet.2020.07.042.
https://doi.org/10.1016/j.cclet.2020.07.042
50. Ziyong Li*, Yong-Ji Hu, Kun Zhang, Yiliang Zhang, Qi-Qi Hu, Xiang-Jin Zhang, Xin-Ke Zhang, Yan-Ping Zhu*, Visible light-activated optical switching behaviors of tetra-/triphenylethene-dithienylethene-BF2bdk triad. Author links open overlay panel.
Dyes and Pigments, 2020, 182, 108686. DOI: 10.1016/j.dyepig.2020.108686
49. Ziyong Li*, Chaojun He, Zhiqiang Lu, Pengshou Li, Yan-Ping Zhu*, Recent progress in all-visible-light-triggered diarylethenes.
Dyes and Pigments, 2020, 182, 108623. DOI: 10.1016/j.dyepig.2020.108623. https://doi.org/10.1016/j.dyepig.2020.108623
48. Ziyong Li*, Yingying Pei, Siteng Hou, Yijie Dai, Duoduo Liu, Junli Zhu, Yan-Ping Zhu*, Xianming Liu*, Dithienylethene-bridged difluoroboron β-diketonate dyes: Optical switching behaviors and triple sensing for volatile amine vapors.
Dyes and Pigments, 2020, 108419, DOI: 10.1016/j.dyepig.2020.108419. https://doi.org/10.1016/j.dyepig.2020.108419
47. Ziyong Li*, Yufei Song, Zhiqiang Lu, Zixu Li, Rong Li, Yunshuang Li, Siteng Hou, Yan-Ping Zhu*, Hui Guo*, Novel difluoroboron complexes of curcumin analogues as “dual-dual” sensing materials for volatile acid and amine vapors.
Dyes and Pigments, 2020, 108406, DOI: 10.1016/j.dyepig.2020.108406. https://doi.org/10.1016/j.dyepig.2020.108406
46. Weng, W.-Z., Wei-Zhao Weng, Jiang-Shan Guo, Kai-Xuan Liu, Tian-Qi Shao, Li-Qun Song, Yan-Ping Zhu*, Yuan-Yuan Sun*, Qing-Guo Meng*, Canadian Journal of Chemistry, 2020, 98, 179-183. DOI: 10.1139/cjc-2019-0456
https://www.nrcresearchpress.com/doi/10.1139/cjc-2019-0456#.Xo_qILEs-4w
45. Z.-H., Shang, J.-N., Sun, J.-S., Guo, Y.-Y., Sun, W.-Z., Weng, Z.-X., Zhang, Z.-J., Li, Y.-P., Zhu* , Facile synthesis of 1,3,4-oxadiazoles via iodine promoted oxidative annulation of methyl-azaheteroarenes and hydrazides
Tetrahedron, 2020, 76, 130887(封面文章), https://doi.org/10.1016/j.tet.2019.130887
44. Chen Chen*, Jinghui Zhao, Xiaonan Shi, Liying Liu, Yan-Ping Zhu, Wan Sun, Bolin Zhu*, Recent advances in cyclization reactions of unsaturated oxime esters (ethers): synthesis of versatile functionalized nitrogen-containing scaffolds.
Org. Chem. Front. 2020, 7, 1948-1969. DOI: 10.1039/D0QO00397B, https://doi.org/10.1039/D0QO00397B
43. Chen Chen*, Liying Liu, Wan Sun, Jie Ding, Yan-Ping Zhu, Bolin Zhu*, Pd/NBE-catalyzed sequential carbamoylation/olefination of aryl iodides.
Org. Chem. Front. 2020, 7, 3179-3185. DOI: 10.1039/d0qo00905a
42. Chen Chen*, Yuebo Wang, Xiaonan Shi, Wan Sun, Jinghui Zhao, Yan-Ping Zhu, Liying Liu, Bolin Zhu*, Palladium-Catalyzed C-2 and C-3 Dual C-H Functionalization of Indoles: Synthesis of Fluorinated Isocryptolepine Analogues.
Organic Letters 2020, DOI: 10.1021/acs.orglett.0c01159. https://dx.doi.org/10.1021/acs.orglett.0c01159
41. Chen Chen*, Wan Sun, Yan Yan, Fang Yang, Yuebo Wang, Yan‐Ping Zhu, Liying Liu, Bolin Zhu*, Palladium-Catalyzed Phosphoryl‐Carbamoylation of Alkenes: Construction of Nonbenzylic C(sp3 )−P(O)R2 Bonds via C(sp 3 )−Pd(II)−P(O)R2 Reductive Elimination.
Adv. Synth. Catal. 2020, 362, 2970-2975， DOI: 10.1002/adsc.202000337. https://doi.org/10.1002/adsc.202000337
40. Wan Sun, Xiaonan Shi, Chen Chen*, Yan-Ping Zhu, Zhengyu Liu, Bolin Zhu*, Palladium-Catalyzed Cascade Cyclization/Alkynylation of Alkene-Tethered Carbamoyl Chlorides with Terminal Alkynes: Synthesis of Alkyne-Functionalized Oxindoles.
Asia. J. Org. Chem. 2020, 9, 575-578. DOI：10.1002/ajoc.202000033. https://doi.org/10.1002/ajoc.202000033
39. Weng, W.-Z., Gao, Y.-H., Zhang, X., Liu, Y.-H., Shen, Y.-J, Zhu, Y.-P.*, Sun, Y.-Y., Meng, Q.-G., Wu, A.-X.*.
Org. Biomol. Chem. 2019, 17, 2087-2091. https://pubs.rsc.org/en/content/articlelanding/2019/OB/C9OB00033J#!divAbstract
38. Cheng, Y.; Xiang, J.; Wang, Z.; Ma, J.; Wang, M.; Tang, B.; Wu, Y.; Zhu, Y.-P.*; Wu, A.-X.*.
Adv. Synth. Catal. 2018, 360, 550-555.
https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201701130
————————————————————————————————
Before YTU
————————————————————————————————
37. Zhu, Y.-P.; Mampuys, P.; Sergeyev, S.; Ballet, S.; Maes. B.*
Adv. Synth. Catal. 2017, 359, 2481-2498. https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201700134
36. Zhu, Y.-P.; Sergeyev, S.; Franck, P.; Orru, R.; Maes. B.*
Org. Lett. 2016, 18, 4602-4605. https://pubs.acs.org/doi/10.1021/acs.orglett.6b02247
35. Mampuys, P.; Zhu, Y.-P.; Sergeyev, S.; Ruijter, E.*; Orru, R. V. A.; Van Doorslaer, S.; Maes, B. U. W.*
Org. Lett. 2016, 18, 2808–2811. https://pubs.acs.org/doi/10.1021/acs.orglett.6b01023
34. Mampuys, P.; Zhu, Y.-P.; Vlaar, T.; Ruijter, E.*; Orru, R. V. A.*; Maes, B. U. W.*
Angew. Chem. Int. Ed. 2014, 53, 12849-12854. https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201406717
33. Zhu, Y.-P.; Fei, Z.; Liu, M.-C.; Jia, F.-C.; Wu, A.-X.*
Org. Lett. 2013, 15, 378-381. https://pubs.acs.org/doi/10.1021/ol303331g
32. Zhu, Y.-P.; Liu, M.-C.; Jia, F.-C.; Yuan, J.-J.; Gao, Q.-H.; Lian, M.; Wu, A.-X.*
Org. Lett. 2012, 14, 3392-3395. https://pubs.acs.org/doi/10.1021/ol301366p
31. Zhu, Y.-P.; Lian, M.; Jia, F.-C.; Liu, M.-C.; Yuan, J.-J.; Gao, Q.-H.; Wu, A.-X.*,
Chem. Commun. 2012, 48, 9086-9088. https://pubs.rsc.org/en/content/articlelanding/2012/CC/c2cc34561g#!divAbstract
30. Zhu, Y.-P.; Jia, F.-C.; Liu, M.-C.; Wu, A.-X.*, Org. Lett. 2012, 14, 4414-4417. (IF: 6.579，一区)
https://pubs.acs.org/doi/10.1021/ol301921t
29. Zhu, Y.-P.; Jia, F.-C.; Liu, M.-C.; Wu, L.-M.; Cai, Q.; Gao, Y.; Wu, A.-X.*, Org. Lett. 2012, 14, 5378-5381.
https://pubs.acs.org/doi/10.1021/ol302613q
28. Zhu, Y.-P.; Gao, Q.-H.; Lian, M.; Yuan, J.-J.; Liu, M.-C.; Zhao, Q.; Yang, Y.; Wu, A.-X.*, Chem. Commun. 2011, 47, 12700-12702.
https://pubs.rsc.org/en/content/articlelanding/2011/CC/c1cc15819h#!divAbstract
27. Zhu, Y.-P.; Liu, M.-C.; Cai Q.; Jia, F.-C.; Wu, A.-X.*, Chem. Eur. J. 2013, 19, 10132-10137.
https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201301734
26. Zhu, Y.-P.; Cai Q.; Jia, F.-C.; Liu, M.-C.; Gao, Q.-H.; Meng, X.-G.; Wu, A.-X.* Tetrahedron 2014, 70, 9536–9544.
https://doi.org/10.1016/j.tet.2014.10.052
25. Zhu, Y.-P.; Cai Q.; Gao, Q.-H.; Jia, F.-C.; Liu, M.-C.; Gao, M.; Wu, A.-X.*, Tetrahedron 2013, 69, 6392-6398.
https://doi.org/10.1016/j.tet.2013.05.106
24. Fei, Z.; Zhu, Y.-P.*; Liu, M.-C.; Jia, F.-C.; Wu, A.-X.* Tetrahedron Lett. 2013, 54, 1222-1226. (通讯作者)
https://doi.org/10.1016/j.tetlet.2012.12.072
23. Zhu, Y.-P.; Yuan, J.-J.; Zhao, Q.; Lian, M.; Gao, Q.-H.; Liu, M.-C.; Yang, Y.; Wu, A.-X.*, Tetrahedron 2012, 68, 173-178.
https://doi.org/10.1016/j.tet.2011.10.074
22. Zhu, Y.-P.; Yuan, J.-J.; Li, Y.-T.; Gao, M.; Cao, L.-P.; Ding, J.-Y.; Wu, A.-X.*, Synlett. 2011, 52-56.
https://sci-hub.tw/10.1055/s-0030-1259102
21. Jia, F.-C.; Zhu, Y.-P.; Liu, M.-C.; Lian, M.; Gao, Q.-H.; Cai, Q.; Wu, A.-X.* Tetrahedron 2013, 69, 7038-7044.
https://doi.org/10.1016/j.tet.2013.06.054
20. Cai, Q.; Zhu, Y.-P.; Gao, Y.; Sun, J.-J.; Wu, A.-X.* Can. J. Chem. 2013, 91, 414-419.
https://www.nrcresearchpress.com/doi/10.1139/cjc-2012-0534
19. Gao, Q.-H.; Zhu, Y.-P.; Lian, M.; Liu, M.-C.; Yuan, J.-J.; Yin, G.-D.*; Wu, A.-X.* J. Org. Chem. 2012, 77, 9865-9870.
https://doi.org/10.1021/jo301751e
18. Yuan, J.-J.; Zhu, Y.-P.; Lian, M.; Gao, Q.-H.; Liu, M.-C.; Jia, F.-C.; Wu, A.-X.* Tetrahedron Lett. 2012, 53, 1222-1226.
https://doi.org/10.1016/j.tetlet.2011.12.099
17. Li, Y.-T.; Zhu, Y.-P.; Qin, J.; Guo, H.-Z.; Li, L.; Wu, A.-X.* Synlett. 2009, 2028-2034.
https://sci-hub.tw/10.1055/s-0029-1217528
16. Li, Y.-T.; Zhu, Y.-P.; Wu, A.-X.* Chin. J. Struct. Chem. 2009, 28, 1593-1596 Gao,
15. Gao, Q.-H.; Fei, Z.; Zhu, Y.-P.; Lian, M.; Jia, F.-C.; Liu, M.-C.; She, N.-F.*; Wu, A.-X.* Tetrahedron 2013, 69, 22-28.
https://doi.org/10.1016/j.tet.2012.10.072
14. Xue, W.-J.; Li, Q.; Zhu, Y.-P.; Wang, J.-G.; Wu, A.-X.* Chem. Commun. 2012, 48, 3485-3487.
https://pubs.rsc.org/en/content/articlelanding/2012/CC/c2cc18077d#!divAbstract
13. Lian, M.; Li, Q.; Zhu, Y.-P.; Yin, G.-D.; Wu, A.-X.* Tetrahedron 2012, 68, 9598-9605.
https://doi.org/10.1016/j.tet.2012.09.056
12. Li, Y.-T.; Li, L.; Zhu, Y.-P.; Meng, X.-G.; Wu, A.-X.* Crystal Growth & Design 2009, 9, 4255-4257.
11. Pang, T.; Sun, Y.; Xue, W.-J.; Zhu, Y.-P.; Yu, G.-A.*; Wu, A.-X.* Adv. Synth. Catal. 2013, 355, 2208-2216.
https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201201049
10. Wang, J.-G.; Wang, M.; Xiang, J.-C.; Zhu, Y.-P.; Xue, W.-J.; Wu, A.-X.* Org. Lett. 2012, 14, 6060-6063.
https://doi.org/10.1021/ol302950w
9. Xue, W.-J.; Li, Q.; Gao, F.-F.; Zhu, Y.-P.; Wang, J.-G.; Zhang, W.; Wu, A.-X.* ACS Combinatorial Science 2012, 18, 478-483.
8. Deng, C.; Yang, Y.; Gao, M.; Zhu, Y.-P.; Wu, A.-X.* Ma, J.-R.; Yin, G.-D.* Tetrahedron 2012, 68, 3828-3834.
https://doi.org/10.1016/j.tet.2012.03.049
7. Gao, Q.-H.; Wu, X.; Jia, F.-C.; Liu, M.-C.; Zhu, Y.-P.; Cai, Q.; Wu, A.-X.* J. Org. Chem. 2013, 78, 2798.
https://pubs.acs.org/doi/10.1021/jo302754c
6. Shu, W.-M.; Yang, Y.; Zhang, D.-X.; Wu, L.-M.; Zhu, Y.-P.; Yin, G.-D.; Wu, A.-X.* Org. Lett. 2013, 15, 456-459.
https://doi.org/10.1021/ol400016c
5. Ding, J.-Y.; Cao, L.-P.; Wang, J.-G.; Xue, W.-J.; Zhu, Y.-P.; Wu, A.-X.* J. Chem. Res. 2011, 35,298-301.
https://journals.sagepub.com/doi/abs/10.3184/174751911X13053065216840
4. Zhang, D. X.; Yang, Y.; Gao, M.; Shu, W. M.; Wu, L. M.; Zhu, Y. P.; Wu, A. X.*, Oxides. Tetrahedron 2013, 69, 1849-1856.
https://doi.org/10.1016/j.tet.2012.12.060
3. Li, L.; Fei, Z.; Meng, X.-G.; Cao, L.-P.; Pang, T.; Zhu, Y.-P.; Wu, A.-X.*, Chin. J. Struct. Chem. 2013, 24, 97-104.
2. Wu, L.; Yang, Y.; Gao, M.; Zhang, D.; Shu, W.; Zhu, Y.-P.; Wu, A.-X.*, Temperature. Synlett. 2012, 2137-2141.
https://sci-hub.tw/10.1055/s-0031-1290433
1. Yang, Y.; Gao, M.; Wu, L.-M.; Deng, C.; Zhang, D.-X.; Gao, Y.; Zhu, Y.-P.; Wu, A.-X.*, Tetrahedron 2011, 67, 5142-5149.
https://doi.org/10.1016/j.tet.2011.05.058
![Graphical abstract: Oxidative C(sp3)–H functionalization of methyl-azaheteroarenes: a facile route to 1,2,4-triazolo[4,3-a]pyridines](https://pubs.rsc.org/en/Image/Get?imageInfo.ImageType=GA&imageInfo.ImageIdentifier.ManuscriptID=C9OB00033J&imageInfo.ImageIdentifier.Year=2019)
