Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Zaigang Luo"'
Publikováno v:
Molecules, Vol 17, Iss 9, Pp 10652-10666 (2012)
A series of novel 6-(pyrazolylmethyl)-4-oxo-4H-quinoline-3-carboxylic acid derivatives bearing different substituents on the N-position of quinoline ring were designed and synthesized as potential HIV-1 integrase (IN) inhibitors, based on the structu
Externí odkaz:
https://doaj.org/article/ca20d11c8bda46b4b620811a1077b8c7
Publikováno v:
Energy Sources, Part A: Recovery, Utilization, and Environmental Effects. 45:4050-4063
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e70700e51d5facfc15c6f4e5c3b1389
https://doi.org/10.1080/15567036.2023.2201180
https://doi.org/10.1080/15567036.2023.2201180
Autor:
Haoran Feng, Kojo Aboagye Nartey, Tao Zhu, Li Rui, Chen-Fu Liu, Zaigang Luo, Liu Qiannan, Xuemei Xu
Publikováno v:
Asian Journal of Organic Chemistry. 10:926-930
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7ba43449dd09fdd43f44a8de6d20f65
https://doi.org/10.1002/ajoc.202100112
https://doi.org/10.1002/ajoc.202100112
Publikováno v:
Synthesis. 52:1067-1075
Intermolecular [4+2]/[3+2] radical annulation of N-methylanilines with alkynoates under metal- and photoredox-catalyst-free conditions provides a practical and efficient method to synthesize bioactive 1,4-dihydroquinolines and pyrrolo[1,2-a]quinoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c0f521fdda2630f7b67e4b4170d53b5
https://doi.org/10.1055/s-0039-1691541
https://doi.org/10.1055/s-0039-1691541
Publikováno v:
Letters in Organic Chemistry. 16:735-739
The synthesis of the calix[4]arene derivative containing 1,3-diketo moieties via direct Claisen condensation without protection of the unsubstituted phenolic OH groups is reported. Single crystal X-ray diffraction analysis reveals that the calix unit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de46ba280b1f70977601f7d2f35fb22c
https://doi.org/10.2174/1570178615666181102121349
https://doi.org/10.2174/1570178615666181102121349
Publikováno v:
Advanced Synthesis & Catalysis. 361:3086-3093
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2674138a805d95fb464c4a12cb126ad2
https://doi.org/10.1002/adsc.201900221
https://doi.org/10.1002/adsc.201900221
Autor:
Yonghong Liu, Ding Li, Liang Xu, Junfeng Wang, Xuefeng Zhou, Zaigang Luo, Huayan Xu, Shengrong Liao, Bin Yang, Xiaowei Luo
Publikováno v:
Tetrahedron. 75:2785-2796
A transition-metal-free insertion of benzyl group between aldehyde and imidazole of 2-(1H-benzo[d]imidazol-1-yl)benzaldehyde was achieved for the first time. Two diverse sets of quinolin-4-one derivatives: benzo[4,5]imidazo[1,2-a]quinolin-5(7H)-ones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473653767801f816d3f06f191557d872
https://doi.org/10.1016/j.tet.2019.03.058
https://doi.org/10.1016/j.tet.2019.03.058
Publikováno v:
Chemical Communications. 55:4027-4030
We demonstrated herein an Fe(iii)-mediated radical alkylation of quinones. A wide range of bioactive molecules with quinone motifs can be rapidly synthesized by using readily available and inexpensive NaBH4/NaBD4 with alkenes at room temperature unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fe670a09e1de4e303f833de36957312
https://doi.org/10.1039/c9cc01704f
https://doi.org/10.1039/c9cc01704f
Publikováno v:
Organic Chemistry Frontiers. 5:3299-3305
A copper-catalyzed decarboxylative and oxidative decarbonylative cross-coupling of cinnamic acids with aliphatic aldehydes was achieved. The reaction undergoes subsequent decarbonylation, radical addition and decarboxylation processes with aliphatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::385c8caee6ed65c6c457efe5ebf13915
https://doi.org/10.1039/c8qo00927a
https://doi.org/10.1039/c8qo00927a
Autor:
Baoxia Liang, Liang Xu, Junfeng Wang, Huayan Xu, Shengrong Liao, Bin Yang, Yonghong Liu, Xuefeng Zhou, Xiuping Lin, Zaigang Luo
Publikováno v:
Tetrahedron. 77:131764
Terminal allylic alcohols are important motifs in natural products, and also key intermediates/precursors in numerous novel reaction transformations. In this study, enabled by a bifunctional ligand featuring a basic amino group, a gold-catalyzed hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::356d67770d4fc55a68db792552ce11a4
https://doi.org/10.1016/j.tet.2020.131764
https://doi.org/10.1016/j.tet.2020.131764