Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Yue-Jin Liu"'
Autor:
Yueliuting Fu, Cui-Hong Chen, Mao-Gui Huang, Jun-Yang Tao, Xu Peng, Hai-Bing Xu, Yue-Jin Liu, Ming-Hua Zeng
Publikováno v:
ACS Catalysis. 12:5036-5047
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca422b454dfb072793f8481e789255f
https://doi.org/10.1021/acscatal.2c00839
https://doi.org/10.1021/acscatal.2c00839
Autor:
Wen-Tao Ma, Mao-Gui Huang, Yueliuting Fu, Zhong-Hui Wang, Jun-Yang Tao, Jia-Wei Li, Yue-Jin Liu, Ming-Hua Zeng
Publikováno v:
Chemical Communications. 58:7152-7155
We report a phosphine-directed ruthenium-catalyzed C8-selective alkylation of naphthalenes with alkenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f648eb0d384b3416b461f21cdef23bfb
https://doi.org/10.1039/d2cc02161g
https://doi.org/10.1039/d2cc02161g
Publikováno v:
The Journal of Organic Chemistry. 86:11915-11925
Modification of commercially available biaryl monophosphine ligands via ruthenium(II)-catalyzed P(III)-directed-catalyzed ortho C-H secondary alkylation is described. The use of highly ring-strained norbornene as a secondary alkylating reagent is the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a482d8996de6ba7f7dcc5ee77041953e
https://doi.org/10.1021/acs.joc.1c01329
https://doi.org/10.1021/acs.joc.1c01329
Autor:
Wen-Tao, Ma, Mao-Gui, Huang, Yueliuting, Fu, Zhong-Hui, Wang, Jun-Yang, Tao, Jia-Wei, Li, Yue-Jin, Liu, Ming-Hua, Zeng
Publikováno v:
Chemical communications (Cambridge, England). 58(51)
We report a phosphine-directed ruthenium-catalyzed C8-selective alkylation of naphthalenes with alkenes. This protocol provides straightforward access to a large library of electron-rich C8-alkyl substituent 1-naphthphosphines, which outperformed com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ca71e11a6a6e0fedb90ca22b80f5334
https://pubmed.ncbi.nlm.nih.gov/35667557
https://pubmed.ncbi.nlm.nih.gov/35667557
Publikováno v:
Advanced Synthesis & Catalysis. 363:2843-2849
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d98580983bdbc85733d5c6f6a0cb745
https://doi.org/10.1002/adsc.202100283
https://doi.org/10.1002/adsc.202100283
Publikováno v:
Asian Journal of Organic Chemistry. 10:1113-1116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba042c2b85087c1e365168f263c0884e
https://doi.org/10.1002/ajoc.202100161
https://doi.org/10.1002/ajoc.202100161
Publikováno v:
Organic Letters. 23:2057-2062
Herein, we disclose a ruthenium-catalyzed meta-selective C-H activation of phosphines by using intrinsic P(III) as a directing group. 2,2,6,6-Tetramethylheptane-3,5-dione acts as the ligand and exhibits an excellent performance in boosting the meta-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0a7fd6d125606861b2d27eb0d6d3f5c
https://doi.org/10.1021/acs.orglett.1c00237
https://doi.org/10.1021/acs.orglett.1c00237
Publikováno v:
Chinese Journal of Chemistry. 38:1545-1552
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84f7c6a87704cd24caae89fdea52f390
https://doi.org/10.1002/cjoc.202000246
https://doi.org/10.1002/cjoc.202000246
Publikováno v:
ACS Catalysis. 10:8212-8222
In the presence of accessible β-C–H bonds, γ-C–H activation of saturated aliphatic carboxamides remains unresolved because β-C–H activation is kinetically favored. This is almost a dogma in the dev...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7abe6df4400adadfc898fbecfa5958a
https://doi.org/10.1021/acscatal.0c02025
https://doi.org/10.1021/acscatal.0c02025
Autor:
Ming-Hua Zeng, Mohamedally Kurmoo, Yue-Jin Liu, Rou-Ming Peng, Pan-Ting Tang, Yi Wei, Jia-Wei Li, Xiao-Peng Luo, Zheng-Xin Zhou, Abing Duan
Publikováno v:
Organic Letters. 22:4129-4134
Biphenylcarboxylic acid with two competing C(sp2)-H sites was designed for site selective C(sp2)-H functionalization by developing carboxylic acids assisted remote and selective olefination via 7-membered palladacycle. Mechanism investigation and DFT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e01368ee338f8bbb99d4aa624f68b035
https://doi.org/10.1021/acs.orglett.0c01208
https://doi.org/10.1021/acs.orglett.0c01208