Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Mingyou Hu"'
Autor:
Peizhuo Yao, Yinbin Zhang, Shuqun Zhang, Xinyu Wei, Yanbin Liu, Chong Du, Mingyou Hu, Cong Feng, Jia Li, Fang Zhao, Chaofan Li, Zhen Li, Lisha Du
Publikováno v:
Frontiers in Oncology, Vol 12 (2023)
ObjectiveAntibody-drugs conjugates (ADCs) are novel drugs with highly targeted and tumor-killing abilities and developing rapidly. This study aimed to evaluate drug discovery and clinical trials of and explore the hotspots and frontiers from 2012 to
Externí odkaz:
https://doaj.org/article/76359dbe626d43708efbded0a52195f2
Autor:
Huanhuan Song, Weihao Li, Xiaoying Wang, Kaiteng Wang, Jingwen Li, Shuai Liu, Pin Gao, Xin-Hua Duan, Jinbo Hu, Mingyou Hu
Publikováno v:
CCS Chemistry. :1-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fa981f15ff395027da7e221fda365fe
https://doi.org/10.31635/ccschem.023.202302980
https://doi.org/10.31635/ccschem.023.202302980
Publikováno v:
The Journal of Organic Chemistry. 88:3787-3793
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e071d599b1a0335f9cf7ef0336e50a7
https://doi.org/10.1021/acs.joc.2c03062
https://doi.org/10.1021/acs.joc.2c03062
Publikováno v:
Nanoscale. 15:5705-5711
Functional nanocomposites fabricated by growing CsPbBr3 perovskite QDs within Fe-doped zeolite X with improved stability for sensitive NH3 detection.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed5b75bc9c3d910212f20e574e0cff61
https://doi.org/10.1039/d2nr06923g
https://doi.org/10.1039/d2nr06923g
Autor:
Chunyu Zhao, Haixia Song, Yinghao Chen, Wei Xiong, Mingyou Hu, Youshen Wu, Yanfeng Zhang, Ling He, Yi Liu, Aizhao Pan
Publikováno v:
ACS Energy Letters. 7:4389-4397
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99a1f23b686a0cc9d5b83c429102f605
https://doi.org/10.1021/acsenergylett.2c02293
https://doi.org/10.1021/acsenergylett.2c02293
Publikováno v:
Organic Chemistry Frontiers. 9:966-972
A practical method for the synthesis of allylic thioacyanates from allylic alcohols was disclosed employing K2S2O8 as the oxidant and NH4SCN as the thiocyanate source.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb746fb667e9a02837cb598de5d1b3b6
https://doi.org/10.1039/d1qo01710a
https://doi.org/10.1039/d1qo01710a
Autor:
Keyuan Zhang, Yulong Wang, Chonglong He, Youkang Zhou, Danning Wang, Mingyou Hu, Xin-Hua Duan, Le Liu
Publikováno v:
Organic Chemistry Frontiers. 9:5599-5605
A simple and catalyst-free radical addition/1,2-aryl migration cascade process of ally alcohol driven by halogen bond was developed under visible light irradiation, featuring mild conditions, practical procedures, and broad substrate scope.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b6f7d9f2298d268d74cf78500bbc904
https://doi.org/10.1039/d2qo01035f
https://doi.org/10.1039/d2qo01035f
Autor:
Yueyun Bao, Mingyou Hu, Jinbo Hu, Xin Liu, Yu-Rou Zhao, Hunahuan Song, Junjie Zhang, Xinxin Han, Xiaoying Wang, Xin-Hua Duan, Le Liu
Publikováno v:
Organic Chemistry Frontiers. 9:204-209
An efficient trifluoromethylation reaction of vinyldiazoacetates under mild reaction conditions was depicted.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b187b44998ce6b6537b858ae5d929e48
https://doi.org/10.1039/d1qo01654g
https://doi.org/10.1039/d1qo01654g
Publikováno v:
Angewandte Chemie. 132:8585-8589
A Cu-catalyzed gem-bis(trifluoromethyl)olefination of α-diazo esters, using TMSCF3 as the only fluorocarbon source, has been developed and provides an exquisite method to access gem-bis(trifluoromethyl)alkenes. This unprecedented olefination process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14c722e3978270ce7b3d7d69947160ee
https://doi.org/10.1002/ange.202002409
https://doi.org/10.1002/ange.202002409
Publikováno v:
Organic Letters. 21:5500-5504
A visible-light-driven sulfamate esters guided alkylation of unactivated C(sp3)-H bonds enabled by a 1,6-HAT/radical addition cascade is described. Not only structurally diverse Michael acceptors but also styrenes are amenable to this alkylation reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f95c2f805bcce5ee58f5c6c0ebf67911
https://doi.org/10.1021/acs.orglett.9b01804
https://doi.org/10.1021/acs.orglett.9b01804