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Akademický článek

Recent Advances in Electrochemically Mediated Reactions of Diselenides

Autor: Lei Zhan, Qian Wang, Hai-Tao Tang, Zu-Yu Mo, Ying-Ming Pan

Publikováno v: SynOpen, Vol 07, Iss 04, Pp 521-534 (2023)

Externí odkaz: https://doaj.org/article/722b0a47ddd54139ad1251ec1785233e

Electrochemical oxidative cascade cyclization of olefinic amides and alcohols leading to the synthesis of alkoxylated 4H-3,1-benzoxazines and indolines

Autor: Wan-Jie Wei, Lei Zhan, Cai-Na Jiang, Hai-Tao Tang, Ying-Ming Pan, Xian-Li Ma, Zu-Yu Mo

Publikováno v: Green Chemistry. 25:928-933

We have developed a mild and efficient electrochemical oxidative strategy to construct anticancer alkoxylated 4H-3,1-benzoxazines and indolines without the requirement for a transition-metal catalyst and an external oxidant.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f6b86224d5361ffd677725385037e8ee
https://doi.org/10.1039/d2gc04645h

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Synthesis of Selenyl-Substituted Quinoline Derivatives via Substrate-Controlled Three-Component Domino Reactions

Autor: Shuang-Shuang Sun, Zu-Yu Mo, Yan-Yan Chen, Yan-Li Xu

Publikováno v: The Journal of Organic Chemistry. 87:12447-12454

A simple and efficient method for the preparation of selenyl-substituted quinoline derivatives through a C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0075e917c4d0c40a8eda710ae89ea00
https://doi.org/10.1021/acs.joc.2c01260

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Electrochemically-mediated C–H functionalization of allenes and 1,3-dicarbonyl compounds to construct tetrasubstituted furans

Autor: Mu-Xue He, Yan Yao, Chun-Zhi Ai, Zu-Yu Mo, Yu-Zheng Wu, Qi Zhou, Ying-Ming Pan, Hao-Tao Tang

Publikováno v: Organic Chemistry Frontiers. 9:781-787

We reported an electrocatalytic C–H activation method to construct novel highly functionalized tetrasubstituted furan derivatives, which uses allenes and 1,3-dicarbonyl compounds as substrates.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0af0d4257e0c7278ac6e44948bc5d2e9
https://doi.org/10.1039/d1qo01458g

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Synthesis and biological evaluation of novel 1,3-diphenylurea quinoxaline derivatives as potent anticancer agents

Autor: Hai-Tao Tang, Li Yang, Xiao-Lin Cao, Zu-Yu Mo, Gui-Zhen Li, Xi-Lin Ouyang, Yao Gu, Ying-Ming Pan

Publikováno v: Medicinal Chemistry Research. 30:1496-1511

A series of 1,3-diphenylurea quinoxaline derivatives were synthesized and characterized by 1H, 13C NMR, and HR-ESI-MS analyses. In vitro cytotoxicity of the synthesized compounds was evaluated by MTT assay against MGC-803, H460, T-24, HeLa, HepG2, an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ff1dd6fdc4ed6d853d0d7c59e8dc769
https://doi.org/10.1007/s00044-021-02745-2

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Ni(ii), Cu(ii) and Zn(ii) complexes with the 1-trifluoroethoxyl-2,9,10-trimethoxy-7-oxoaporphine ligand simultaneously target microtubules and mitochondria for cancer therapy

Autor: Cheng Hou, Hong Liang, Zu-Yu Mo, Gui-Fa Su, Zhen-Feng Chen, Yin Chen, Lan-Shan Liao

Publikováno v: Inorganic Chemistry Frontiers. 8:2225-2247

Metal complexes of [NiL2(NO3)2] (1), [CuL2(NO3)2] (2) and [ZnL2(NO3)2] (3) with the 1-trifluoroethoxyl-2,9,10-trimethoxy-7-oxoaporphine (L) ligand were synthesized. We discovered that complexes 1–3 exhibited considerable anticancer activity in vitr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::235c9b68ea32c939afd7e8f2d60cf2e3
https://doi.org/10.1039/d0qi01463j

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Electrocatalytic Synthesis of gem-Bisarylthio Enamines and α-Phenylthio Ketones via a Radical Process under Mild Conditions

Autor: Xiu-Jin Meng, Hai-Tao Tang, Qian-Yu Li, Zu-Yu Mo, Ying-Ming Pan, Yong-Zhou Pan, Shi-Yan Cheng

Publikováno v: Synlett. 32:593-600

The novel method for the synthesis of gem-bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0aff41a1404ed72bf64ecdf39815c5a7
https://doi.org/10.1055/a-1335-7902

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