Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Chun-Xiang Kuang"'
Autor:
Zi-Kang Xing, Li-Sha Du, Xin Fang, Heng Liang, Sheng-Nan Zhang, Lei Shi, Chun-Xiang Kuang, Tian-Xiong Han, Qing Yang
Publikováno v:
Neural Regeneration Research, Vol 18, Iss 6, Pp 1300-1307 (2023)
In Alzheimer’s disease, the transporter P-glycoprotein is responsible for the clearance of amyloid-β in the brain. Amyloid-β correlates with the sphingomyelin metabolism, and sphingomyelin participates in the regulation of P-glycoprotein. The amy
Externí odkaz:
https://doaj.org/article/64e2fc3729724cc38cd5c1bf52ff8510
Autor:
Zi-Kang Xing, Li-Sha Du, Xin Fang, Heng Liang, Sheng-Nan Zhang, Lei Shi, Chun-Xiang Kuang, Tian-Xiong Han, Qing Yang
Publikováno v:
Neural Regeneration Research; Jun2023, Vol. 18 Issue 6, p1300-1307, 11p
Publikováno v:
Chinese Chemical Letters. 22:571-574
A novel and convenient iron-catalyzed ketonization of 2-aryl-1,1-dibromoalkenes with KOAc has been achieved. A series of α -acetoxy aryl ketones were prepared with moderate yields via 2-carbon position functionalization of 2-aryl-1,1-dibromoalkenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::176fa945c520c942e3c19a72bd2c3f5b
https://doi.org/10.1016/j.cclet.2010.11.022
https://doi.org/10.1016/j.cclet.2010.11.022
Publikováno v:
Chinese Chemical Letters. 22:310-313
An efficient and mild protocol for bromination of aryl azides with N-bromosuccinimide (NBS) under FeCl3 catalysis in 1,2-dichloroethane was developed. It is proved to be an efficient method for obtaining brominated aryl azides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::855c0748d5f8298a08a63f23c4b53743
https://doi.org/10.1016/j.cclet.2010.10.024
https://doi.org/10.1016/j.cclet.2010.10.024
Autor:
Chun Xiang Kuang, Yu Bo Jiang
Publikováno v:
Chinese Chemical Letters. 20:545-548
A convenient one-pot synthesis of functionalized ( E )-2-arylvinyl bromides was achieved by microwave-induced deacetylation and subsequent acylation using dicyclohexyl carbodiimide (DCC) and dimethylamino-pyridine (DMAP) at room temperature from ( E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::514bce6dd9dfc63742b1701eae5f1aff
https://doi.org/10.1016/j.cclet.2009.01.020
https://doi.org/10.1016/j.cclet.2009.01.020
Publikováno v:
Chinese Chemical Letters. 20:48-51
One-pot simultaneous debrominative decarboxylation and sulfamation of anti -2,3-dibromo-3-(4-chlorosulfonylphenyl)propanoic acid in DMF (for alkyl amines) or DMF-pyridine (for aryl amines) using a diverse range of alkyl and aryl amines under microwav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c891e7c971f0b9a78bc8118184b9099
https://doi.org/10.1016/j.cclet.2008.10.004
https://doi.org/10.1016/j.cclet.2008.10.004
Publikováno v:
ChemInform. 42
A novel and convenient iron-catalyzed ketonization of 2-aryl-1,1-dibromoalkenes with KOAc has been achieved. A series of α -acetoxy aryl ketones were prepared with moderate yields via 2-carbon position functionalization of 2-aryl-1,1-dibromoalkenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76cd482502f12918082772982f704db9
https://doi.org/10.1002/chin.201132064
https://doi.org/10.1002/chin.201132064
Publikováno v:
ChemInform. 42
An efficient and mild protocol for bromination of aryl azides with N-bromosuccinimide (NBS) under FeCl3 catalysis in 1,2-dichloroethane was developed. It is proved to be an efficient method for obtaining brominated aryl azides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e86dfbd16bd8d251ab097ea9078673c
https://doi.org/10.1002/chin.201120077
https://doi.org/10.1002/chin.201120077
Autor:
Chun Xiang Kuang, Yu Bo Jiang
Publikováno v:
ChemInform. 40
A convenient one-pot synthesis of functionalized ( E )-2-arylvinyl bromides was achieved by microwave-induced deacetylation and subsequent acylation using dicyclohexyl carbodiimide (DCC) and dimethylamino-pyridine (DMAP) at room temperature from ( E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9714d21def09bb573ae52e81178a42ff
https://doi.org/10.1002/chin.200936041
https://doi.org/10.1002/chin.200936041
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3ce2370f11569df1cdb2053310798ea
https://doi.org/10.1002/chin.200925072
https://doi.org/10.1002/chin.200925072