Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Xinqiang Tan"'
Autor:
Xueyan Du, Xiaozhe Yang, Han Wang, Xinguang Li, Murong Wang, Xiang Li, Ye Tao, Yaxing Yang, Xinqiang Tan, Feng Ren, Ping-Xin Zhou, Yong-Min Liang
Publikováno v:
Organic Chemistry Frontiers. 10:898-904
A palladium/norbornene-catalyzed ortho-amination/allylation of aryl iodides was developed for the construction of ortho-aminated allylbenzene by using N-benzoyloxyamine as the amination reagent and homoallyl alcohol as the allylation reagent.
Publikováno v:
Advanced Materials. 35
Highly efficient and stable single-stack hybrid white organic light-emitting diode (WOLED) devices are developed using two emissive layers, one with amber colored phosphorescent molecular aggregate emission from the Pd (II) complex, Pd(II) 7-(3-(pyri
Autor:
Ping-Xin Zhou, Xiaozhe Yang, Xueyan Du, Shujie Zhao, Han Wang, Xinguang Li, Ning Liu, Xinqiang Tan, Feng Ren, Yong-Min Liang
Publikováno v:
Organic Chemistry Frontiers. 9:4097-4103
A palladium-catalyzed reaction of aryl iodide-tethered alkenes with homoallyl alcohols is reported, providing a convenient and efficient approach to C(sp3)–allylation products.
Autor:
Ping-Xin Zhou, Xiaozhe Yang, Xueyan Du, Shujie Zhao, Han Wang, Xinqiang Tan, Jia Wang, Yong-Min Liang
Publikováno v:
Organic Chemistry Frontiers. 9:2606-2611
A palladium-catalyzed cis-selective carboalkylation of internal alkynes with cyclobutanols is reported, providing a useful and facile approach to alkyl-substituted olefins with moderate to good yields and excellent stereoselectivity.
Autor:
Ping-Xin Zhou, Xiaozhe Yang, Xueyan Du, Shujie Zhao, Han Wang, Xinqiang Tan, Jia Wang, Yong-Min Liang
Publikováno v:
Organic Chemistry Frontiers. 9:3640-3640
Correction for ‘Pd-Catalyzed alkynyl aryl iodide cyclization/alkylation with cyclobutanols’ by Ping-Xin Zhou et al., Org. Chem. Front., 2022, 9, 2606–2611, https://doi.org/10.1039/D2QO00180B.
Publikováno v:
Organic Letters. 19:1634-1637
The silver-catalyzed Hunsdiecker bromination of aliphatic carboxylic acids is described. With Ag(Phen)2OTf as the catalyst and dibromoisocyanuric acid as the brominating agent, various aliphatic carboxylic acids underwent decarboxylative bromination
Publikováno v:
Journal of the American Chemical Society. 140(19)
The copper-assisted radical carbofluorination of unactivated alkenes with fluoride ions is described. With [Cu(L3)F2]H2O (L3 = 4,4'-di(methoxycarbonyl)-2,2'-bipyridine) as the fluorine source and [Ag(DMPhen)(MeCN)]BF4 (DMPhen = 2,9-dimethyl-1,10-phen
Publikováno v:
Journal of the American Chemical Society. 139(36)
The silver-catalyzed decarboxylative trifluoromethylation of aliphatic carboxylic acids is described. With AgNO3 as the catalyst and K2S2O8 as the oxidant, the reactions of aliphatic carboxylic acids with (bpy)Cu(CF3)3 (bpy = 2,2′-bipyridine) and Z
Publikováno v:
Angewandte Chemie (International ed. in English). 56(48)
Direct fluorination of tertiary alkyl bromides and iodides with Selectfluor reagent is described. The halogen-exchange fluorination proceeds efficiently in acetonitrile at room temperature under metal-free conditions and exhibits a wide range of func
Publikováno v:
Journal of the American Chemical Society. 139(29)
The copper-mediated trifluoromethylation of alkyl radicals is described. The combination of Et3SiH and K2S2O8 initiates the radical reactions of alkyl bromides or iodides with BPyCu(CF3)3 (BPy = 2,2′-bipyridine) in aqueous acetone at room temperatu