Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Dachuan Qiu"'
Autor:
Meixian Yang, Xinyue Huang, Wenjun Miao, Lan Yi, Jiajing Cai, Zhenghuan Zhao, Jia He, Dachuan Qiu
Publikováno v:
Organic Chemistry Frontiers. 10:1975-1980
We describe here a method to generate both benzoyl fluorides and benzoic acids using 2,5-cyclohexadienones prepared from phenols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70aeff01543c1b70acde5e702e990535
https://doi.org/10.1039/d3qo00183k
https://doi.org/10.1039/d3qo00183k
Autor:
Muyao Li, Jianfeng Bao, Jie Zeng, Linlin Huo, Xinxin Shan, Xintong Cheng, Dachuan Qiu, Wenjun Miao, Xianglong Zhu, Guoming Huang, Kaiyuan Ni, Zhenghuan Zhao
Publikováno v:
Journal of Colloid and Interface Science. 626:364-373
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::521060c9254c564cdfdaa8010d3fa2a0
https://doi.org/10.1016/j.jcis.2022.06.118
https://doi.org/10.1016/j.jcis.2022.06.118
Autor:
Lan Yi, Xinyue Huang, Meixian Yang, Jiajing Cai, Jianhua Jia, Zhiping Peng, Zhenghuan Zhao, Fengyuan Yang, Dachuan Qiu
Publikováno v:
Bioorganicmedicinal chemistry letters.
Cytochrome P450 1B1 (CYP1B1) is highly expressed in a variety of tumors and implicated to drug resistance. More and more researches have suggested that CYP1B1 is a new target for cancer prevention and therapy. Various CYP1B1 inhibitors with a rigid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::270f36b16076093279d112e08e8d8a28
https://pubmed.ncbi.nlm.nih.gov/36565966
https://pubmed.ncbi.nlm.nih.gov/36565966
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 88:129263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454be870964f4aedfc034110d503af8c
https://doi.org/10.1016/j.bmcl.2023.129263
https://doi.org/10.1016/j.bmcl.2023.129263
Autor:
Lan Yi, Xinyue Huang, Meixian Yang, Jiajing Cai, Jianhua Jia, Zhiping Peng, Zhenghuan Zhao, Fengyuan Yang, Dachuan Qiu
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0393791cd29b1f5c6fe011e47e302d87
https://doi.org/10.2139/ssrn.4287701
https://doi.org/10.2139/ssrn.4287701
Publikováno v:
Angewandte Chemie International Edition. 58:18513-18518
A convenient and efficient domino aryne process was developed under transition-metal-free conditions to generate a range of tetra- and pentacyclic ring systems. This transformation was realized via a 1,2-benzdiyne through a nucleophilic and Diels-Ald
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8011b574f607d8285d6a6b3604767f
https://doi.org/10.1002/anie.201911730
https://doi.org/10.1002/anie.201911730
Autor:
Muyao Li, Linlin Huo, Jie Zeng, Guifen Zhu, Saige Shi, Xiangqing Liu, Xianglong Zhu, Guoming Huang, Dachuan Qiu, Jianhua Jia, Kaiyuan Ni, Zhenghuan Zhao
Publikováno v:
Chemical Engineering Journal. 440:135966
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06695809a36e86482ff46b23638d7a8b
https://doi.org/10.1016/j.cej.2022.135966
https://doi.org/10.1016/j.cej.2022.135966
Publikováno v:
Accounts of chemical research. 53(2)
Polysubstituted arenes are prevalent in numerous natural products, medicines, agrochemicals, and organic functional materials. Among methods to prepare polysubstituted arenes, pathways involving benzyne intermediates are particularly attractive given
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8f3580d3b982015eeed74d193ebc49
https://pubmed.ncbi.nlm.nih.gov/31984723
https://pubmed.ncbi.nlm.nih.gov/31984723
Publikováno v:
Journal of the American Chemical Society. 140:13214-13218
A unique approach toward the preparation of cyclohexenynone equivalents was successfully developed via oxidative dearomatization of aryne precursors, featuring multiple functionalities on the target rings. Upon activation, these in situ formed cycloh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc79bb3845646f4503a3b231dca17fe1
https://doi.org/10.1021/jacs.8b08915
https://doi.org/10.1021/jacs.8b08915
Publikováno v:
Organic Letters. 18:3726-3729
Vicinal diamination of domino aryne precursors was achieved with sulfamides. The reaction proceeds through a two-aryne pathway, accepting two N-nucleophiles at the 1,2-positions of an arene ring. Symmetrical and unsymmetrical diaminobenzenes were rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93d952db60536929c4617a9aef9b8b41
https://doi.org/10.1021/acs.orglett.6b01747
https://doi.org/10.1021/acs.orglett.6b01747