Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Wenzhu Bi"'
Autor:
Aleksic, Sandra, Eisenberg, Ruth, Tsomos, Effie, Zahedpour Anaraki, Sara, Japp, Emily, Upadhyay, Laxmi, Mowrey, Wenzhu Bi, Akalin, Enver, Zonszein, Joel
Publikováno v:
In Diabetes Research and Clinical Practice July 2020 165
Akademický článek
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Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 195:359-366
A one-pot synthetic strategy was developed for the synthesis of heterocyclic 1,4,2-oxazaphosphinanes via a three component Kabachnik-Fields reaction of 2-aminophenol, diphenyl H-phosphonate and car...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31b38990d17e64db0ec203edc17f3c77
https://doi.org/10.1080/10426507.2019.1700417
https://doi.org/10.1080/10426507.2019.1700417
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 192:887-895
A series of biologically important 3/4-sulfonylquinoline derivatives was synthesized starting from easily available sodium benzenesulfinates, diethyl H-phosphonate and 2-substituted quinoline N-oxi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a543b7f4a5e3ce43af7cd4320b749b9
https://doi.org/10.1080/10426507.2017.1315422
https://doi.org/10.1080/10426507.2017.1315422
Publikováno v:
Tetrahedron. 73:2439-2446
An efficient one-pot synthesis of β-ketophosphonates has been developed, via the reaction of α,β-alkenyl carboxylic acids or alkenes with H-phosphonates and air oxygen, catalyzed by CuSO4·5H2O in CH3CN. CH3CN plays a decisive role, probably by fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4589f61fce9c434fd42ca2217d205125
https://doi.org/10.1016/j.tet.2017.03.026
https://doi.org/10.1016/j.tet.2017.03.026
Publikováno v:
Asian Journal of Organic Chemistry. 6:492-495
A synthetic strategy for an iodine-mediated sulfonylation of quinoline N-oxides has been developed. A wide variety of 2-sulfonyl quinoline derivatives were synthesized by reacting various quinoline N-oxides with different sodium sulfinates in the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23c45593ebfe1f2da2b6c76b4aa587e3
https://doi.org/10.1002/ajoc.201700001
https://doi.org/10.1002/ajoc.201700001
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 192:391-396
The present reaction provides a simple and convenient synthetic strategy to construct β-iodovinyl sulfones through molecular iodine and DTBP (di-tert-butyl peroxide) promoted difunctionalization of alkynes with sodium benzenesulfinates under mild an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73d637500933d14a489a5ec25b68edc3
https://doi.org/10.1080/10426507.2016.1259622
https://doi.org/10.1080/10426507.2016.1259622
Autor:
Likun Duan, Shaohua Zhu, Yufen Zhao, Lingbo Qu, Hai-Tao Wu, Wenzhu Bi, Kai Sun, Chen Qu, Xiaolan Chen, Xu Li
Publikováno v:
Organic Chemistry Frontiers. 4:1595-1600
An efficient one-pot methodology for C2-selective amination and alkylation of quinoline N-oxides towards 2-substituted quinolines was developed, via the reaction of various quinoline N-oxides with ammonia, a large variety of primary and secondary ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e217ddc00fc2c40473aec617def2207f
https://doi.org/10.1039/c7qo00311k
https://doi.org/10.1039/c7qo00311k
Autor:
Grober, Ellen1 (AUTHOR) ellen.grober@einstein.yu.edu, Mowrey, Wenzhu Bi2 (AUTHOR), Ehrlich, Amy R.3 (AUTHOR), Mabie, Peter1 (AUTHOR), Hahn, Steven4 (AUTHOR), Lipton, Richard B.1,2 (AUTHOR)
Publikováno v:
Journal of Clinical & Experimental Neuropsychology. Nov2016, Vol. 38 Issue 9, p1038-1049. 12p. 1 Diagram, 8 Charts.
Publikováno v:
Inorganica Chimica Acta. 443:299-303
A microporous metal–organic framework [InL][(CH3)2NH2]·(H4L = 9-(3,5-dicarboxyphenyl)carbazole-3,6-dicarboxylic acid) (1) was hydrothermally synthesized and structurally characterized by single crystal X-ray diffraction and powder X-ray diffractio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eab98ba04c89c0c7b91af2d52fbb728
https://doi.org/10.1016/j.ica.2016.01.014
https://doi.org/10.1016/j.ica.2016.01.014