Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Shou-ren Zhang"'
Autor:
Da-Yong Fan, Qing-Lai Dang, Cheng-Yang Xu, Chuang-Dao Jiang, Wang-Feng Zhang, Xin-Wu Xu, Xiao-Fang Yang, Shou-Ren Zhang
Publikováno v:
Frontiers in Plant Science, Vol 11 (2020)
There are considerable variations in the percentage loss of hydraulic conductivity (PLC) at mid-day minimum water potential among and within species, but the underpinning mechanism(s) are poorly understood. This study tested the hypothesis that plant
Externí odkaz:
https://doaj.org/article/ac7f4c9296b34496aa2554f82ac70e48
Autor:
Lu Shen, Jin-Wei Yuan, Bing Zhang, Sai-Yi Song, Liang-Ru Yang, Yong-Mei Xiao, Shou-Ren Zhang, Ling-Bo Qu
Publikováno v:
Zeitschrift für Naturforschung B. 78:245-260
An environmentally friendly strategy for the photo-catalyzed three-component reaction between quinoxalin-2(1H)-ones, vinylarenes, with inexpensive and easily accessible ethyl bromodifluoroacetate/sodium difluoromethanesulfinate is described. This pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da4fbc8dae4edd20374ecb9bc9ff94a5
https://doi.org/10.1515/znb-2022-0126
https://doi.org/10.1515/znb-2022-0126
Autor:
Chen-Xu Mou, Jin-Wei Yuan, Qian Hu, Bing-Jie Han, Liang-Ru Yang, Yong-Mei Xiao, Lu-Lu Fan, Shou-Ren Zhang, Ling-Bo Qu
Publikováno v:
New Journal of Chemistry. 47:3783-3792
A convenient and efficient copper-catalyzed oxidative C3-cyanoarylation of quinoxalin-2(1H)-ones is developed using 3-aminoindazoles as efficient arylating agents via the cleavage of two C–N bonds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f853a852f1cbd84542ea7cde4003dc13
https://doi.org/10.1039/d2nj04309b
https://doi.org/10.1039/d2nj04309b
Autor:
Jin-Wei Yuan, Mei-Yue Zhang, Yan Liu, Wen-Yu Hu, Liang-Ru Yang, Yong-Mei Xiao, Xiao-Qiong Diao, Shou-Ren Zhang, Jian Mao
Publikováno v:
Organic & Biomolecular Chemistry. 20:9722-9733
A mild and efficient transition metal-free radical difluoroarylmethylation/cyclization of unactivated alkenes toward the synthesis of quinazolinone derivatives with easily accessible α,α-difluoroarylacetic acids has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc1dccf23e988f0c9db00a2cdea200c3
https://doi.org/10.1039/d2ob01904c
https://doi.org/10.1039/d2ob01904c
Autor:
Jin-Wei Yuan, Lu Shen, Meng-Yao Ma, Shi Feng, Wan Yang, Liang-Ru Yang, Yong-Mei Xiao, Shou-Ren Zhang, Ling-Bo Qu
Publikováno v:
New Journal of Chemistry. 46:4470-4482
A visible-light-catalyzed difluoroacetylated spirocyclization of N-arylpropiolamides with ethyl bromodifluoroacetate as a CF2CO2Et radical precursor is described using fac-[Ir(ppy)3] as a photocatalyst.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bcfccb0cc3b340d68c355a78629b599
https://doi.org/10.1039/d2nj00131d
https://doi.org/10.1039/d2nj00131d
Autor:
Jin-Wei Yuan, Guang-Chao Huang, Li-Li Wang, Xin-Yuan Wang, Liang-Ru Yang, Shou-Ren Zhang, Pu Mao, Yong-Mei Xiao, Ling-Bo Qu
Publikováno v:
Zeitschrift für Naturforschung B. 77:75-85
A practical and efficient synthetic route to construct a variety of 3-arylselenenyl/3-arylthio spiro[4.5]trienones was developed using Selectfluor reagent as a mild oxidant. This reaction proceeds via a sequence of electrophilic cation addition, spir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72bb93795012e6ef977b9129c933e377
https://doi.org/10.1515/znb-2021-0154
https://doi.org/10.1515/znb-2021-0154
Autor:
Yongmei Xiao, Wen-Yu Hu, Liangru Yang, Jinwei Yuan, Shou-Ren Zhang, Pu Mao, Yang Zhang, Chen-Xu Mou, Lingbo Qu
Publikováno v:
Organic & Biomolecular Chemistry. 19:10348-10358
A practical synthetic route to construct a variety of 3-benzyl spiro[4,5]trienones was developed via transition-metal Cu/Ag-catalyzed oxidative ipso-annulation of activated alkynes with unactivated toluenes using TBPB as an oxidant under microwave ir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f55feb48e589861480effb8e8d5e68e3
https://doi.org/10.1039/d1ob01970h
https://doi.org/10.1039/d1ob01970h
Autor:
Shou-Ren Zhang, Meng-Yao Ma, Liangru Yang, Lingbo Qu, Jinwei Yuan, Guang-Chao Huang, Yang Zhang, Pu Mao, Teng-Yu Yang
Publikováno v:
Organic Chemistry Frontiers. 8:6937-6949
A site-specific oxidative C–H chalcogenation of quinoxalin-2(1H)-ones with various diaryl diselenides/disulfides is presented by employing Selectfluor reagent as an oxidant. The reaction proceeds selectively at the C6 position of quinoxalin-2(1H)-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d171473ff305aea51be529b2f15e3b7
https://doi.org/10.1039/d1qo01332g
https://doi.org/10.1039/d1qo01332g
Publikováno v:
The Science of the total environment. 848
Although the effects of nitrogen deposition on tree water relations are studied extensively, its impact on the relative sensitivities of stomatal and xylem hydraulic conductance to vapor pressure deficit and water potential is still poorly understood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::540965bedfa3baa080eaf4e736ceda75
https://pubmed.ncbi.nlm.nih.gov/35934026
https://pubmed.ncbi.nlm.nih.gov/35934026
Autor:
Fang Peng, Lingbo Qu, Yan-Chun Li, Jinwei Yuan, Liang-Yu Yang, Jun-Liang Zhu, Pu Mao, Hu-Lin Zhu, Shou-Ren Zhang
Publikováno v:
Organic Chemistry Frontiers. 7:273-285
A practical transition-metal free decarboxylative coupling reaction of oxamic acids with quinoxalin-2(1H)-ones has been developed under mild conditions. This transformation provides an efficient approach for the preparation of 3-carbamoyl quinoxalin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d69afa2fb1b58c0e0f10402353b8678
https://doi.org/10.1039/c9qo01322a
https://doi.org/10.1039/c9qo01322a