Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shu-Qiang Yin"'
Publikováno v:
Letters in Organic Chemistry. 16:911-914
This study introduces a concise and efficient method for preparing diacetoxyiodoarenes from the corresponding iodoarenes. In the presence of acetic anhydride, iodoarenes were oxidized to diacetoxyiodoarenes by sodium perborate in acetic acid under ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8772089ec87eb53d3e34b5f70ac8dbe
https://doi.org/10.2174/1570178616666181203142445
https://doi.org/10.2174/1570178616666181203142445
Publikováno v:
Research on Chemical Intermediates. 42:5387-5394
2,6-Diiododiaryl ethers are not only useful blocks to construct substituted diaryl ethers but are also characteristic drug precursors. In this research, a one-pot tandem oxidation of phenols substituted with electron-withdrawing group at the para pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39da224b738305c253ef3bad44843b6a
https://doi.org/10.1007/s11164-015-2373-y
https://doi.org/10.1007/s11164-015-2373-y
Publikováno v:
Tetrahedron: Asymmetry. 24:320-323
Racemic 8-ethoxy-2-(4-fluorophenyl)-3-nitro-2 H -chromene (S14161) was recently identified as a potent inhibitor of phosphoinositide 3-kinase (PI3K). In order to investigate the effects of its two enantiomers on tumor cell lines, we designed a novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::982e9e28ca1aeca5245ce4713087e9c7
https://doi.org/10.1016/j.tetasy.2013.02.009
https://doi.org/10.1016/j.tetasy.2013.02.009
Publikováno v:
Current Medicinal Chemistry. 19:1021-1035
Methionine aminopeptidases (MetAPs), which remove methionine residue from newly synthesized polypeptide chains, are a class of metalloproteases ubiquitously distributed in both eukaryotes and prokaryotes. MetAP-2 inhibition can induce G1 cell cycle a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ce5924d23bd12a6093abb226292eb06
https://doi.org/10.2174/092986712799320709
https://doi.org/10.2174/092986712799320709
Autor:
Xinliang Mao, Kunkun Han, Xiaolin Du, Min Shi, Zhao-Peng Liu, Shu-Qiang Yin, Ting-Ting Kong, Cheng-Mei Zhang, Zubin Zhang, Long-Qian Tang, Biyin Cao
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(11)
The small chemical compound 8-ethoxy-2-(4-fluorophenyl)-3-nitro-2H-chromene (S14161) was recently identified as an inhibitor of the phosphoinositide 3-kinase (PI3K). In the present study, we designed a novel synthesis of S14161 and prepared a series
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::491e9f001cb89c3e3f2cc364c2e6527c
https://pubmed.ncbi.nlm.nih.gov/23601711
https://pubmed.ncbi.nlm.nih.gov/23601711
Efficient syntheses of quinolizidine-type poison-frog alkaloids via Michael-type conjugate addition.
Autor:
De-Jun Zhou, Yang-Yang Zhai, Ji-Chuan Kong, Zhen-Hui Wang, Xue-Yun Gong, Mei Huang, Shu-Qiang Yin
Publikováno v:
Journal of Chemical Research; Apr2018, Vol. 42 Issue 4, p227-232, 6p