Zobrazeno 1 - 10
of 16
pro vyhledávání: '"You-lin Deng"'
Autor:
Yang Yang, Zhen-Zhen Ren, Wu-Jun Wei, Zhi-Long He, You-Lin Deng, Zhuan Wang, Yu-Chun Fan, Jie Zhou, Li-He Jiang
Publikováno v:
Pharmaceutical Biology, Vol 60, Iss 1, Pp 1566-1577 (2022)
Context Urolithin A (UroA) can inhibit the growth of many human cancer cells, but it has not be reported if UroA inhibits nasopharyngeal carcinoma (NPC) cells.Objective To explore the inhibitory effect of UroA on NPC and potential mechanism in vitro.
Externí odkaz:
https://doaj.org/article/ab1d4abca20b47c49c2a59ff7bb27204
Autor:
Tian Wang, Lin-li Zhang, Qing-hui Feng, Meng-ling Wang, Yu-Chun Fan, Zhuan Wang, You-lin Deng, Li-He Jiang
Background Many recent studies have reported the role of WGCNA in liver cancer, and screened out modules related to the clinical characteristics of liver cancer. The prognostic role of modular genes provides a reference for the treatment of liver can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c37198571d45b536ba2f8e8f532721c0
https://doi.org/10.21203/rs.3.rs-895710/v1
https://doi.org/10.21203/rs.3.rs-895710/v1
Autor:
Liang-Neng Wang, Li Yuan, Ruilong Sheng, Zhi-Yuan Peng, Zeng-Zeng Li, Shi Tang, You-Lin Deng, Gui-Xiu Huang
Publikováno v:
Tetrahedron Letters. 58:2127-2130
A feasible approach to 2-azaspirocyclic cyclohexadienones via visible-light-induced perfluoroalkylation cyclization of N -benzylacrylamides was reported. Using R f -X (X = I or Br) as the R f radical source, the reaction underwent a cascade radical a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aff40bdc153559c82f234314afcdb5e3
https://doi.org/10.1016/j.tetlet.2017.04.055
https://doi.org/10.1016/j.tetlet.2017.04.055
Publikováno v:
Tetrahedron Letters. 58:329-332
An effective visible-light-induced perfluoroalkylation of conjugated tosyl amides using R f -X (X = I or Br) as the R f source by Ir photocatalyst was disclosed. This protocol provides a new way to prepare oxindoles or α -aryl- β -fluoroalkyl amide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3be5ca68c04afcc2df7bff050f509178
https://doi.org/10.1016/j.tetlet.2016.12.027
https://doi.org/10.1016/j.tetlet.2016.12.027
Autor:
Li Yuan, Ruilong Sheng, Shi-Lu Chen, Zeng-Zeng Li, Wen-Xin Wang, Ying-Chun Wang, Shi Tang, You-Lin Deng, Jie Li
Publikováno v:
Chemical Communications. 52:4470-4473
A novel copper-catalyzed aerobic oxidative cyclization of benzamides via meta-selective C-H tert-alkylation using AIBN and analogues as radical precursors was described. This strategy provides an elusive and rapid means to 7-tert-alkylated isoquinoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c9de3c6354d1439cbfb5aaa9219b90
https://doi.org/10.1039/c5cc10464e
https://doi.org/10.1039/c5cc10464e
Autor:
Jie Li, Zhu-Ping Xiao, Wen-Xin Wang, Ruilong Sheng, Ying-Chun Wang, You-Lin Deng, Shi Tang, Guo-Liang Ding, Ming-Wei Wang
Publikováno v:
The Journal of Organic Chemistry. 80:12599-12605
A novel visible-light-induced carboperfluoroalkylation of alkenes using perfluoroalkyl iodides and bromides as Rf sources, leading to isoquinoline-1,3-diones, was developed. This method offers rapid entry to perfluorinated isoquinoline-1,3(2H,4H)-dio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67341989b0d2a7e359c14d79cd5ad608
https://doi.org/10.1021/acs.joc.5b01803
https://doi.org/10.1021/acs.joc.5b01803
Autor:
Jie Li, Ruilong Sheng, Guo-Liang Ding, Ming-Wei Wang, Shi Tang, You-Lin Deng, Li Yuan, Zeng-Zeng Li
Publikováno v:
Organicbiomolecular chemistry. 14(39)
A simple and efficient copper-controlled divergent cyclization of benzamides, which leads to perfluorinated or cyanated isoquinolinediones, is developed. In the presence of AIBN, methacryloyl benzamides with perfluoroalkyl iodides undergo cascade rad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e119ea797a4a3c8ba8f44c5c6fd75f20
https://pubmed.ncbi.nlm.nih.gov/27714180
https://pubmed.ncbi.nlm.nih.gov/27714180
Autor:
Shi-Lu Chen, Shi Tang, Ruilong Sheng, Li Yuan, Jie Li, Zeng-Zeng Li, Wen-Xin Wang, You-Lin Deng, Ying-Chun Wang
Publikováno v:
ChemInform. 47
A novel copper-catalyzed aerobic oxidative cyclization of benzamides via meta-selective C–H tert-alkylation using AIBN and analogues as radical precursors was described. This strategy provides an elusive and rapid means to 7-tert-alkylated isoquino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddd791a507b8b6b0d042c32bb3c5661b
https://doi.org/10.1002/chin.201630185
https://doi.org/10.1002/chin.201630185
Autor:
Jie Li, Ruilong Sheng, You-Lin Deng, Zhu-Ping Xiao, Ming-Wei Wang, Guo-Liang Ding, Wen-Xin Wang, Ying-Chun Wang, Shi Tang
Publikováno v:
ChemInform. 47
A novel visible-light-induced carboperfluoroalkylation of alkenes using perfluoroalkyl iodides and bromides as Rf sources, leading to isoquinoline-1,3-diones, was developed. This method offers rapid entry to perfluorinated isoquinoline-1,3(2H,4H)-dio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5f7c5d04c14065d7126ad8a003f6804
https://doi.org/10.1002/chin.201619144
https://doi.org/10.1002/chin.201619144
Autor:
Shi Tang, Zhi-Hao Li, You-Lin Deng, Dong Zhou, Li-Ya Liu, Shu-Hua Li, Guo-Liang Ding, Qian Zhang
Publikováno v:
ChemInform. 46
Azobisisobutyronitrile is used as radical source in a copper-catalyzed oxidative cyanopropylation reaction with N-arylacryl amides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecb8247320c81b4793c819489a6fb4f4
https://doi.org/10.1002/chin.201532123
https://doi.org/10.1002/chin.201532123