Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xing-Li Zhu"'
Publikováno v:
Organic Letters. 16:2192-2195
An organocatalytic asymmetric trifluoromethylthiolation reaction via in situ generation of active electrophilic trifluoromethylthio species involving trichloroisocyanuric acid and AgSCF3 as a practical and easily handled electrophilic SCF3 source for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::521d23e0a916e55b87053fb86961b9ac
https://doi.org/10.1021/ol5006888
https://doi.org/10.1021/ol5006888
Autor:
Xing-Li Zhu, Rongming Wang, Da-Bin Qin, Zeqin Chen, Linhai Jing, Xiaohua Xie, Wujun He, Song Wu
Publikováno v:
Tetrahedron. 69:11084-11091
A series of bispirooxindole derivatives have been synthesized via a cascade Michael-Cyclization reaction between isothiocyanato oxindoles and methyleneindolinones with high yields (up to 98%) and excellent diastereoselectivities (up to >95:5 dr) unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed68bf5ea67c5741e2c1b563acdda708
https://doi.org/10.1016/j.tet.2013.11.016
https://doi.org/10.1016/j.tet.2013.11.016
Autor:
Da-Bin Qin, Linhai Jing, Quan-Zhong Liu, Liang-Liang Yu, Chang-Wu Cai, Zong-Le Zuo, Xing-Li Zhu, Song Wu
Publikováno v:
European Journal of Organic Chemistry. 2013:456-459
Enantioselective Michael addition of oxazolones to in situ generated vinylogous imine intermediates is reported. A series of optically active 3-alkylindole derivatives with adjacent quaternary and tertiary stereocenters was obtained. The resulting ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a5c3d6c70b408066172bea268b06d8c
https://doi.org/10.1002/ejoc.201201335
https://doi.org/10.1002/ejoc.201201335
Autor:
Xing-Li Zhu, Linhai Jing, Quan-Zhong Liu, Chang-Wu Cai, Wujun He, Liang-Liang Yu, Da-Bin Qin, Zong-Le Zuo
Publikováno v:
Advanced Synthesis & Catalysis. 354:2965-2970
An organocatalytic asymmetric vinylogous Michael addition of dicyanoolefins to vinylogous imine intermediates generated in situ from arenesulfonylalkylindoles has been developed. This protocol provides an easy and convenient approach to C-3 alkyl-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7115e29108130170b1e04a5c59195eee
https://doi.org/10.1002/adsc.201200286
https://doi.org/10.1002/adsc.201200286
Publikováno v:
ChemInform. 45
This new one-pot protocol allows the synthesis of a wide range of different substituted and SCF3 functionalized oxindole derivatives under mild condition by using simple starting materials.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddbc3b228780c8b124907fd3ec99b9c4
https://doi.org/10.1002/chin.201442123
https://doi.org/10.1002/chin.201442123
Autor:
Linhai Jing, Wujun He, Xing-Li Zhu, Rongming Wang, Song Wu, Xiaohua Xie, Da-Bin Qin, Zeqin Chen
Publikováno v:
ChemInform. 45
The diastereoselective synthesis of bisspirooxindoles (III) and (VI) is accomplished through a consecutive Michael addition/cyclization reaction of methyleneindolinones with 3-isothiocyanato oxindoles in the presence of small amounts of tetramethylgu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::669bc496a635d7e53a9e1e16589f17d1
https://doi.org/10.1002/chin.201424124
https://doi.org/10.1002/chin.201424124
Autor:
Linhai Jing, Chang-Wu Cai, Song Wu, Zong-Le Zuo, Liang-Liang Yu, Xing-Li Zhu, Quan-Zhong Liu, Da-Bin Qin
Publikováno v:
ChemInform. 44
For the first time the highly stereoselective title Michael addition reaction is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::802321a6b3dbd269c3cf849fd4da959e
https://doi.org/10.1002/chin.201322121
https://doi.org/10.1002/chin.201322121
Autor:
Wujun He, Linhai Jing, Chang-Wu Cai, Quan-Zhong Liu, Zong-Le Zuo, Liang-Liang Yu, Da-Bin Qin, Xing-Li Zhu
Publikováno v:
ChemInform. 44
The present first Michael addition provides an easy and convenient approach to C-3 alkyl-substituted indole derivatives with high enantioselectivities whereas diastereoselectivity depends on the cyano substrate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa63ef011472ce4d36223167dd989ab9
https://doi.org/10.1002/chin.201315102
https://doi.org/10.1002/chin.201315102
Publikováno v:
Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 26(6)
To improve the method for preparing rabbit VX2 liver tumor model and observe the magnetic resonance imaging (MRI) features of the implanted tumors.Sixteen adult New Zealand white rabbits were assigned randomly into 4 equal groups, and VX2 tumor tissu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9d3865ea15ed39b827c845cea02ddae
https://pubmed.ncbi.nlm.nih.gov/16793590
https://pubmed.ncbi.nlm.nih.gov/16793590
Autor:
Zhong-Wei Qu, Wan-Ying Miao, Shu-Qun Hu, Chong Li, Xing-Li Zhuo, Yan-Yan Zong, Yong-Ping Wu, Guang-Yi Zhang
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52788 (2012)
Our laboratory once reported that neuronal nitric oxide synthase (nNOS) S-nitrosylation was decreased in rat hippocampus during cerebral ischemia-reperfusion, but the underlying mechanism was unclear. In this study, we show that nNOS activity is dyna
Externí odkaz:
https://doaj.org/article/a821869e226f4353a3be72fb0d39def8