Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xuefei Zou"'
Autor:
Kemei Lu, Cuicui Lang, Xuefei Zou, Lina Zang, WeiWei Sang, Qian Feng, Ying Mu, Lifeng Liu, Chunhong Xu, Jingrun Zhao
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background New treatment strategies are required against infections caused by Helicobacter pylori, which grows increasingly resistant to antibiotics. Polymerase chain reaction-based methods for antibiotic susceptibility testing are available
Externí odkaz:
https://doaj.org/article/9a01d20ed89546ed8fea798f91929c23
Publikováno v:
Geoenergy Science and Engineering. 222:211409
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e3c29bcbef8d167b47caa1ea0ef3bc3
https://doi.org/10.1016/j.geoen.2022.211409
https://doi.org/10.1016/j.geoen.2022.211409
Autor:
Na Zhang, Wei Liu, Xuefei Zou, Shaochun Wang, Qian Sun, Binfei Li, Songyan Li, Aabiskar Bhusal, Shuhua Wang, Zhaomin Li
Publikováno v:
Fuel. 332:126014
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ac444becca564ffb3195ef06cad1353
https://doi.org/10.1016/j.fuel.2022.126014
https://doi.org/10.1016/j.fuel.2022.126014
Publikováno v:
Journal of Cognitive Neuroscience. 23:1003-1014
To discriminate and to recognize sound sources in a noisy, reverberant environment, listeners need to perceptually integrate the direct wave with the reflections of each sound source. It has been confirmed that perceptual fusion between direct and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bfe7215d7fb1c2529061d747a6303a9
https://doi.org/10.1162/jocn.2010.21470
https://doi.org/10.1162/jocn.2010.21470
Publikováno v:
Tetrahedron. 64:6510-6521
Promoted by triethylamine, α,β-unsaturated N-acylbenzotriazoles reacted with amino compounds in a variety of ways. Thus, N-cinnamoylbenzotriazoles reacting with aromatic amines afforded novel addition products β-benzotriazolyl amides 3, which migh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ded1efe435015137f8060510db3bbf57
https://doi.org/10.1016/j.tet.2008.04.054
https://doi.org/10.1016/j.tet.2008.04.054
Publikováno v:
Synlett. :3042-3046
Amines read with N-cinnamoylbenzotriazoles to afford either β-amino-N-acylbenzotriazoles or cinnamides depending on the structure of the amines. Aromatic amines react with N-cinnamoylbenzotriazoles via 1,4-addition to give β-amino-N-acyl-benzotriaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa484b99c51ee93919ccdf712c71ca28
https://doi.org/10.1055/s-2005-921918
https://doi.org/10.1055/s-2005-921918
Publikováno v:
ChemInform. 39
Promoted by triethylamine, α,β-unsaturated N-acylbenzotriazoles reacted with amino compounds in a variety of ways. Thus, N-cinnamoylbenzotriazoles reacting with aromatic amines afforded novel addition products β-benzotriazolyl amides 3, which migh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::966df2bb499807ce1729bdb70c13671a
https://doi.org/10.1002/chin.200847088
https://doi.org/10.1002/chin.200847088
Publikováno v:
ChemInform. 38
Catalyzed by samarium triiodide (SmI3), substitution of acyl with N‐acylbenzotriazoles for acetyl in acetoacetic esters and acetylacetone proceeds smoothly under neutral conditions in open air, affording the corresponding β‐keto esters and β‐
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdd5df0f6eb81f72f83a839369f19ae1
https://doi.org/10.1002/chin.200744022
https://doi.org/10.1002/chin.200744022
Highly Regioselective Friedel—Crafts Alkylation of Indoles with α,β-Unsaturated N-Acylbenzotriazoles
Publikováno v:
ChemInform. 37
The Friedel–Crafts alkylation rather than acylation of indoles was realized with α,β-unsaturated acylbenzotriazoles catalyzed by samarium(III) iodide under reflux in anhydrous THF. The reaction was highly regioselective, and a series of new 3-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f54f0fe2efbc8ed9b226531a2716b856
https://doi.org/10.1002/chin.200636117
https://doi.org/10.1002/chin.200636117
Publikováno v:
Synlett. 2007:3228-3228
Amines read with N-cinnamoylbenzotriazoles to afford either β-amino-N-acylbenzotriazoles or cinnamides depending on the structure of the amines. Aromatic amines react with N-cinnamoylbenzotriazoles via 1,4-addition to give β-amino-N-acyl-benzotriaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e5a85160dd116aa5bfaa8bcdd7fa2fd
https://doi.org/10.1055/s-2007-990940
https://doi.org/10.1055/s-2007-990940