Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Liangshuo Ji"'
Publikováno v:
Frontiers of Materials Science. 14:488-496
We demonstrate the fabrication of a novel magnetic nanohybrid involving the drug molecule 5-aminolevulinic acid (5-ALA) intercalated Gd-Eu layered rare-earth hydroxide (LRH) coated on magnesium ferrite particles (MgFe2O4). The structure, thermostabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c767b16d94aa4659e0c9cb620a14ab63
https://doi.org/10.1007/s11706-020-0529-1
https://doi.org/10.1007/s11706-020-0529-1
Publikováno v:
Organic Letters. 22:863-866
A novel sp3 C-SCF3 coupling reaction between cycloketone oxime esters and S-trifluoromethyl 4-methylbenzenesulfonothioate was achieved. Ethanol was found to facilitate this transformation by trappi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b2955380a946d38c40b750252e69f94
https://doi.org/10.1021/acs.orglett.9b04343
https://doi.org/10.1021/acs.orglett.9b04343
Publikováno v:
The Journal of organic chemistry. 86(17)
We report the visible-light-promoted selenocyanation of cyclobutanone oxime esters using potassium selenocyanate in the presence of a fac-Ir(ppy)3 catalyst for the first time. Because of the mild conditions employed and use of readily accessible pota
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3b066f46481187bcaeb6f3e0e5f0ce5
https://pubmed.ncbi.nlm.nih.gov/34365792
https://pubmed.ncbi.nlm.nih.gov/34365792
Autor:
Xiancai Zheng, Kui Lu, Xia Zhao, Quan Li, Liangshuo Ji, Yanhong Lin, Xianfu Wei, Miaomiao Tian
Publikováno v:
Tetrahedron Letters. 60:1796-1799
The ferric chloride-promoted direct trifluoromethylselenolation of indoles and other nitrogen-containing heterocyclic compounds in water was performed by employing TsSeCF3 as a trifluoromethylselenolation reagent. The shelf-stable and readily accessi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e5ff5aca5698aa3325cb7430229e709
https://doi.org/10.1016/j.tetlet.2019.06.002
https://doi.org/10.1016/j.tetlet.2019.06.002
Publikováno v:
Organic Chemistry Frontiers. 6:3766-3770
A mild and simple protocol for the synthesis of α-trifluoromethylated ethanone oximes from aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent was developed under transition metal-free conditions. In this three-component reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d14ad2d8fe33d5b6fb4546803c5cea87
https://doi.org/10.1039/c9qo00940j
https://doi.org/10.1039/c9qo00940j
Publikováno v:
Organic letters. 22(3)
A novel sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9022f909bfb7d8505cbcd49a56396244
https://pubmed.ncbi.nlm.nih.gov/31944776
https://pubmed.ncbi.nlm.nih.gov/31944776
Publikováno v:
Tetrahedron Letters. 75:153202
We report the metal-free chalcogenation of cycloketone oxime esters with dichalcogenides via a radical process. Because of the metal-free condition and use of readily accessible dichalcogenides, this method is an effective and green strategy for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38debad390ee9da2b9d7aa1b97b6315f
https://doi.org/10.1016/j.tetlet.2021.153202
https://doi.org/10.1016/j.tetlet.2021.153202
Publikováno v:
Tetrahedron Letters. 72:153071
We report the first metal-free selenolations of pyridinium salts with diselenides to prepare unsymmetrical organoselenides catalysed by visible light. This protocol is an efficient and green method for the preparation of unsymmetrical organoselenides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4455c0e7740441d40da9655e9f8a5f67
https://doi.org/10.1016/j.tetlet.2021.153071
https://doi.org/10.1016/j.tetlet.2021.153071
Publikováno v:
Tetrahedron Letters. 66:152809
A Bronsted acid-promoted trifluoromethylselenolation of benzofurans was disclosed by using Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate as a stable and easily prepared electrophilic trifluoromethylselenolating reagent. A wide range of SeCF3-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8774b7c86b1d8fb7330133d3214e129
https://doi.org/10.1016/j.tetlet.2020.152809
https://doi.org/10.1016/j.tetlet.2020.152809