Zhang Pengxuan

Mr. Zhang Pengxuan


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 October 2014 in Molecules
Verified
Journal Article
Open access
PDF file
ZPZhang Pengxuan
Zhang Pengxuan
YTYuping Tang
Yuping Tang
NLNian-Guang Li
Nian-Guang Li
YZYue Zhu
Yue Zhu
JDJin-Ao Duan
Jin-Ao Duan
Caffeic acid phenethyl ester (CAPE), as one of the main active ingredients of the natural product propolis, shows the unique biological activities such as anti-tumor, anti-oxidation, anti-inflammatory, immune regulation, and so on. These have attracted the attention of many researchers to explore the compound with potent biological activities. This review aims to summarize its bioactivities, synthetic methods and derivatives, which will be helpful for further study and development of CAPE and its derivatives.

25 February 2016 in Molecules
Verified
Journal Article
Open access
PDF file
ZDZe-Xi Dong
Ze-Xi Dong
NLNianguang Li
Nianguang Li
ZPZhang Pengxuan
Zhang Pengxuan
TGTing Gu
Ting Gu
WWWen-Yu Wu
Wen-Yu Wu
ZSZhi-Hao Shi
Zhi-Hao Shi
Scutellarein (2), which is an important in vivo metabolite of scutellarin (1), was synthesized from 3,4,5-trimethoxyphenol (3) in high yield in four steps. This strategy relies on acetylation, aldolization, cyclization and hydrolysis reactions, respectively.

2 June 2015 in Molecules
Verified
Journal Article
Open access
PDF file
WZWei Zhang
Wei Zhang
ZDZe-Xi Dong
Ze-Xi Dong
TGTing Gu
Ting Gu
NLNianguang Li
Nianguang Li
ZPZhang Pengxuan
Zhang Pengxuan
ZSZhi-Hao Shi
Zhi-Hao Shi
In this paper, a new and efficient synthesis of 6-O-methylscutellarein (3), the major metabolite of the natural medicine scutellarin, is reported. Two hydroxyl groups at C-4′ and C-7 in 2 were selectively protected by chloromethyl methyl ether after the reaction conditions were optimized, then 6-O-methyl-scutellarein (3) was produced in high yield after methylation of the hydroxyl group at C-6 and subsequent deprotection of the two methyl ether groups.