Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Yong‐Bin Wang"'
Autor:
Shuai Zhu, Ye-Hui Chen, Yong-Bin Wang, Peiyuan Yu, Shao-Yu Li, Shao-Hua Xiang, Jun-Qi Wang, Jian Xiao, Bin Tan
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Axially chiral compounds have widespread use in asymmetric catalysis. Here, the authors disclose a highly enantioselective synthesis of axially chiral o-naphthoquinones by chiral phosphoric acid catalysis and central-to-axial chirality conversion.
Externí odkaz:
https://doaj.org/article/03c6732f031d4be7b207e6e3dc60046e
Publikováno v:
Cellular & Molecular Biology Letters, Vol 22, Iss 1, Pp 1-10 (2017)
Abstract Background TGF-β1 plays an important role in the epithelial–mesenchymal transition (EMT) of epithelial cancers, including non-small cell lung cancer (NSCLC). While the full underlying mechanism remains unclear, miR-9 is known to play a cr
Externí odkaz:
https://doaj.org/article/b908275f6c924796a4919d6127df3c14
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-9 (2017)
Axially chiral arylquinazolinones are structural motifs in several natural products and can also act as chiral ligands. Here, the authors show a chiral phosphoric acid-catalysed strategy to access enantiomerically pure arylquinazolinones by efficient
Externí odkaz:
https://doaj.org/article/3b59fe05320b44a1be60dbb3f7de7f2f
Publikováno v:
Journal of Integrative Medicine. 21:268-276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92b5076289f4fc96801135e446bcb7c8
https://doi.org/10.1016/j.joim.2023.03.009
https://doi.org/10.1016/j.joim.2023.03.009
Autor:
Li yan Dai, Ren hua Huang, Yun Zhou, Heng le Gu, Yong bin Wang, Ching chong Jack Yang, Xin Xu, Ming Ye, Yong rui Bai, Yu long Liu, Xiao bo Li, Xiu mei Ma
Publikováno v:
Dose-Response, Vol 17 (2019)
The study aimed to develop a novel dose conversion platform by improving linear-quadratic (LQ) model to more accurately describe radiation response for high fraction/acute doses. This article modified the LQ model via piecewise fitting the biological
Externí odkaz:
https://doaj.org/article/e0247ce84628414a9972eb31d50b0e51
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab260a5f8662845a47d61f0a352108b9
https://doi.org/10.1002/anie.202303128
https://doi.org/10.1002/anie.202303128
Publikováno v:
Science China Chemistry. 65:1142-1148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d5b3817d82d93dc9a5cddc1c3c00e6e
https://doi.org/10.1007/s11426-022-1246-8
https://doi.org/10.1007/s11426-022-1246-8
Publikováno v:
Angewandte Chemie International Edition. 62
A Cu/CPA co-catalytic system has been developed for achieving the direct hydrophosphinylation of alkynes with phosphine oxides in delivering novel axially chiral phosphorus-containing alkenes in high yields and excellent enantioselectivities (up to 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299f826004edb9c2c85d64e7aff3c402
https://doi.org/10.1002/anie.202215820
https://doi.org/10.1002/anie.202215820
Autor:
Sheng‐Qi Qiu, Yu Chen, Xiang‐Jun Peng, Shi‐Jiang He, Jun Kee Cheng, Yong‐Bin Wang, Shao‐Hua Xiang, Jun Song, Peiyuan Yu, Junmin Zhang, Bin Tan
Publikováno v:
Angewandte Chemie International Edition. 61
The application of Suzuki-Miyaura coupling reaction to forge the atropisomeric biaryls has seen remarkable progress but exploration of this chemistry to directly forge chiral C(aryl)-C(alkene) axis is underdeveloped. The replacement of arene substrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1a240db57bca40025dfea05a50a4c3
https://doi.org/10.1002/anie.202211211
https://doi.org/10.1002/anie.202211211
Autor:
Shi-qi Ge, Yong-bin Wang, Fei Lin, Run-ran Miao, Kai Zhang, Li Li, Hui-ge Guo, Qian Wang, Li Zhang, Zhi-gang Chen, Guo-an Zhao
Publikováno v:
Atmospheric Pollution Research. 14:101785
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1388aaacab37f4da69ad73b90b4f8b46
https://doi.org/10.1016/j.apr.2023.101785
https://doi.org/10.1016/j.apr.2023.101785