Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Yu-Fei Cheng"'
Autor:
Yu-Fei Cheng, 鄭宇斐
103
The aims of the study. Its purpose is to explore the grieving and readjustment process of bereaved families — including both spouse and children of the deceased family member. Methods. Three participants from the same family, whose beloved
The aims of the study. Its purpose is to explore the grieving and readjustment process of bereaved families — including both spouse and children of the deceased family member. Methods. Three participants from the same family, whose beloved
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/23265921512647639106
Publikováno v:
International Journal of Morphology. 2022, Vol. 40 Issue 5, p1344-1348. 4p.
Autor:
Yan-Jing, Zhang, Si-Si, Wu, Xue-Mei, Chen, Jin-Kui, Pi, Yu-Fei, Cheng, Yi, Zhang, Xiao-Jiao, Wang, Dan, Luo, Jin-Han, Zhou, Jia-Yi, Xu, Xue, Li, Zhuang, Wu, Wei, Jiang, Xiao-Xiao, Wang
Publikováno v:
Journal of Cardiovascular Pharmacology. 79:558-567
As a highly efficient anticancer agent, doxorubicin (DOX) is used for treatment of various cancers, but DOX-induced oxidative damages contribute to a degenerative irreversible cardiac toxicity. Saikosaponin D (SSD), which is a triterpenoid saponin wi
Akademický článek
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Publikováno v:
The Journal of Organic Chemistry. 84:4312-4317
An efficient method for the synthesis of 4-sulfenyl isoxazoles has been developed via AlCl3-mediated electrophilic cyclization/sulfenylation of 2-alkyn-1-one O-methyloximes. Remarkably, N-arylsulfanylsuccinimides are employed as electrophiles for the
Publikováno v:
Organicbiomolecular chemistry. 18(9)
A facile method for the synthesis of 4-chalcogenylated pyrazoles has been developed via electrophilic chalcogenation/cyclization of α,β-alkynic hydrazones. The cyclization of α,β-alkynic aldehyde hydrazones could be induced by using either sulfen
Autor:
Rong Zhou, Yan Qiao, Yu-Fei Cheng, Tao Liu, Wenchao Gao, Honghong Chang, Wenlong Wei, Xing Li
Publikováno v:
The Journal of Organic Chemistry. 82:13459-13467
Switchable ortho/ipso-cyclization of N-arylpropynamides induced with N-sulfanylsuccinimides as general sulfur reagents is reported. In the presence of MeOH, para-fluoro N-arylpropynamides exclusively undergo the ipso-cyclization to give 3-sulfenyl az
Publikováno v:
The Journal of organic chemistry. 84(7)
An efficient method for the synthesis of 4-sulfenyl isoxazoles has been developed via AlCl
Autor:
Yu-Zhu Shang, Yu-Fei Cheng, Xing Li, Honghong Chang, Wei Wenlong, Wenchao Gao, Rong Zhou, Yan Qiao
Publikováno v:
The Journal of organic chemistry. 83(19)
A new and convenient method for one-pot synthesis of α-arylhydrazo-β-keto sulfones is developed via Cu (II)-catalyzed oxysulfonylation/diazenylation of alkenes. This four-component cascade reaction enables a series of α-arylhydrazo-β-keto sulfone
Autor:
Wen-Chao, Gao, Tao, Liu, Yu-Fei, Cheng, Hong-Hong, Chang, Xing, Li, Rong, Zhou, Wen-Long, Wei, Yan, Qiao
Publikováno v:
The Journal of organic chemistry. 82(24)
Switchable ortho/ipso-cyclization of N-arylpropynamides induced with N-sulfanylsuccinimides as general sulfur reagents is reported. In the presence of MeOH, para-fluoro N-arylpropynamides exclusively undergo the ipso-cyclization to give 3-sulfenyl az