Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Shu Rong Ban"'
Publikováno v:
Molecules, Vol 16, Iss 6, Pp 4897-4911 (2011)
A series of novel furan-2-yl(phenyl)methanone derivatives were synthesized, and their structures were established on the basis of 1H-NMR, 13C-NMR and mass spectral data. All the prepared compounds were screened for their in vitro protein tyrosine kin
Externí odkaz:
https://doaj.org/article/be3d2b4ae5c840d1a36c739106e9ae04
Publikováno v:
Molecules, Vol 22, Iss 12, p 2142 (2017)
We previously reported 5,2’-dibromo-2,4’,5’-trihydroxydiphenylmethanoe (LM49), a bromophenol analogue that shows strong protection from oxidative stress injury owing to its superior anti-inflammatory, antioxidant, and anti-apoptotic properties.
Externí odkaz:
https://doaj.org/article/42f8628c66f0440c8bd22fe5ba0af3d6
Autor:
Biao Ma, Hui Xu, Jun Zhang, Hui-Xiong Dai, Junjie Chen, Huiying Wang, Zi-Qiong Guo, Shu‐rong Ban, Mengmeng Wang
Publikováno v:
Chemical communications (Cambridge, England). 57(69)
Herein, we have developed a strategy of sequential C-H activations of indole to construct novel 2-alkynyl aza-spiro[4,5]indole scaffolds, which incorporated both alkyne and spiro-units into indole. Gram-scale synthesis and a one-pot, three-step synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6bb2a3f9af6f38764b202d5f389f6bf
https://pubmed.ncbi.nlm.nih.gov/34373875
https://pubmed.ncbi.nlm.nih.gov/34373875
Publikováno v:
Medicinal Chemistry Research. 28:1319-1337
In the present study, we introduced the nitrogenated heterocycles and fluorine atoms into the 2,5′-dibromo-4,5,2′-trihydroxyl diphenylmethanone (LM49), a bromophenol analog previously reported for its strong antioxidant ability involving in the K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::790c5d97236ea1cf10852aa898a00868
https://doi.org/10.1007/s00044-019-02376-8
https://doi.org/10.1007/s00044-019-02376-8
Publikováno v:
Chirality. 28:721-727
Organocatalysis and aqueous reactions are identified as the focus of the greening of chemistry. Combining these two strategies effectively remains an interesting challenge in organic synthesis. Herein, we used pyrrolidine-based benzoylthiourea 1c to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56b3cb3866746322b793227381e7bcfe
https://doi.org/10.1002/chir.22648
https://doi.org/10.1002/chir.22648
Publikováno v:
Tetrahedron Letters. 61:151780
A palladium-catalyzed fluoroacylation of (hetero)aryl boronic acid with the fluorothioacetates is described at ambient temperature. A variety of aryl, and heteroaryl boronic acids are compatible in the reaction, affording the corresponding fluoroalky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6007af49175294abd40b6c761351159
https://doi.org/10.1016/j.tetlet.2020.151780
https://doi.org/10.1016/j.tetlet.2020.151780
Publikováno v:
Organic Letters. 16:6282-6285
The Z/E selectivity of Pd(II)-catalyzed decarboxylative Heck-type arylations of trans-cinnamaldehydes can be controlled readily by switching the reaction solvent. Depending on the type of solvent used, each of the two isomeric products can be obtaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6895ab2dd87833f6646e40d4dda6816
https://doi.org/10.1021/ol502955r
https://doi.org/10.1021/ol502955r
Autor:
Fei Lang Zheng1, Shu Rong Ban1, Xiu E Feng1, Cheng Xiao Zhao1, Wenhan Lin2, Qing Shan Li1,2 qingshanl@yahoo.com
Publikováno v:
Molecules. Jun2011, Vol. 16 Issue 6, p4897-4911. 15p. 7 Diagrams, 1 Chart.
Publikováno v:
European Journal of Organic Chemistry. 2013:2977-2980
Asymmetric Michael addition of cyclohexanone to nitrostyrenes in the presence of organocatalyst 1 (10 mol-%) and 2,4-dichlorobenzoic acid (10 mol-%) afforded the corresponding synthetically valuable γ-nitroketones in moderate to good yields with hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8f3317d04cb3d0c84c3e7298189a3d
https://doi.org/10.1002/ejoc.201300225
https://doi.org/10.1002/ejoc.201300225
Publikováno v:
Chirality. 28(11)
Organocatalysis and aqueous reactions are identified as the focus of the greening of chemistry. Combining these two strategies effectively remains an interesting challenge in organic synthesis. Herein, we used pyrrolidine-based benzoylthiourea 1c to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21d0dc6759ada92b1f97d711647244c9
https://pubmed.ncbi.nlm.nih.gov/27791318
https://pubmed.ncbi.nlm.nih.gov/27791318