Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Xiang-Zheng Tang"'
Publikováno v:
Future Medicinal Chemistry. 13:601-612
Background: Quinazoline-based compounds have been proved effective in the treatment of cancers for years. Materials & methods: The structural features of several inhibitors of EGFR were integrated and quinazolines with a benzazepine moiety at the 4-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::279d34e17cf6de2f01f3032bf5414f52
https://doi.org/10.4155/fmc-2020-0015
https://doi.org/10.4155/fmc-2020-0015
Autor:
Ming Yan, Ri‐xing Chen, Lei Chen, Zhen-yu Chen, Hua-Ju Liang, Xue-jing Zhang, Xiang-Zheng Tang
Publikováno v:
Advanced Synthesis & Catalysis. 361:3324-3330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be5fadf715cc4a846c4f66eaa1441b57
https://doi.org/10.1002/adsc.201900370
https://doi.org/10.1002/adsc.201900370
Autor:
Yamin Gao, Xiang-Zheng Tang, Yunxiang Tang, Ming Yan, Jie Liang, Tianyu Zhang, Cuiting Fang, Hua-Ju Liang
Publikováno v:
Chemical and Pharmaceutical Bulletin. 67:372-381
A series of meta-amido bromophenol derivatives were designed and synthesized. The compounds were found to potently inhibit the growth of Mycobacterium tuberculosis H37Ra. They also exhibited moderate inhibitory activity against Mycobacterium tubercul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::486fca1765adabf57e8fb90e227ced2a
https://doi.org/10.1248/cpb.c18-00917
https://doi.org/10.1248/cpb.c18-00917
Publikováno v:
Chinese Chemical Letters. 30:395-397
A facile synthesis of tetraarylpyrazoles has been developed via t- BuOK/DMF promoted intermolecular cycloaddition of hydrazones and 1,2-diarylalkynes. A possible reaction pathway via a hydrazone radical is proposed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74c4ac4b0aa2ab7b6f8fe5b46fb5e4c1
https://doi.org/10.1016/j.cclet.2018.06.018
https://doi.org/10.1016/j.cclet.2018.06.018
Autor:
Niu-niu Zhang, Xuan Yining, Shenquan Guo, Ming Yan, Xiang-Zheng Tang, Zhi-feng Mao, Xue-jing Zhang
Publikováno v:
Chinese Chemical Letters. 30:406-408
An efficient synthesis of β-alkoxycarbonyl vinylsulfonium salts had been developed. Their reaction with indene-1,3-diones and other active methylene compounds provided cyclopropane carboxylates in good yields. A tentative reaction mechanism was prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2b6924d849d02ad7f987746902c1dd6
https://doi.org/10.1016/j.cclet.2018.08.021
https://doi.org/10.1016/j.cclet.2018.08.021
Publikováno v:
Tetrahedron Letters. 60:147-149
A straightforward synthesis of isoindolinones has been developed via a [3 + 3] benzannulation of 4-arylmethylene-2,3-dioxopyrrolidines and 1,3-bissulfonylpropenes (or 4-sulfonylcrotonates). A series of functionalized isoindolinones were obtained in e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d163adea74d8455ac93f0636b6fdd1ba
https://doi.org/10.1016/j.tetlet.2018.11.074
https://doi.org/10.1016/j.tetlet.2018.11.074
Publikováno v:
RSC Advances. 7:6660-6663
An asymmetric conjugate addition of t-butyl nitroacetate to in situ generated o-quinone methides had been developed. A chiral squamide derived from 9-amino-9-deoxyepiquinine was found to be the efficient catalyst. α-Nitro-β,β-diaryl-propionates co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b8eeb06d685d6f240b2961a67d52af6
https://doi.org/10.1039/c6ra28068d
https://doi.org/10.1039/c6ra28068d
Autor:
Jie, Liang, Yun-Xiang, Tang, Xiang-Zheng, Tang, Hua-Ju, Liang, Yamin, Gao, Cuiting, Fang, Tian-Yu, Zhang, Ming, Yan
Publikováno v:
Chemicalpharmaceutical bulletin. 67(4)
A series of meta-amido bromophenol derivatives were designed and synthesized. The compounds were found to potently inhibit the growth of Mycobacterium tuberculosis H37Ra. They also exhibited moderate inhibitory activity against Mycobacterium tubercul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::856e7678f21752f1fd3dd390cb56ec3c
https://pubmed.ncbi.nlm.nih.gov/30686792
https://pubmed.ncbi.nlm.nih.gov/30686792
Autor:
Ming Yan, Yong Zou, Xue-jing Zhang, Jie Liang, Lang Tong, Hua-Ju Liang, Albert S. C. Chan, Xiang-Zheng Tang
Publikováno v:
Organicbiomolecular chemistry. 16(19)
A base-mediated [3 + 3] benzannulation strategy for the conversion of 1,3-bis(sulfonyl)propenes and β,γ-unsaturated α-ketoesters to diaryl sulfones has been developed. This method provides facile, metal-free and efficient access to highly substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbeb9a332656327c47a73d11611a152
https://pubmed.ncbi.nlm.nih.gov/29693688
https://pubmed.ncbi.nlm.nih.gov/29693688