Zhen-Hua Wang

Prof. Dr. Zhen-Hua Wang

orcid

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

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

Representative Publications

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15 April 2015 in Organic Letters
Verified
Journal Article
Closed access
JZJian-Qiang Zhao
Jian-Qiang Zhao
MZMing-Qiang Zhou
Ming-Qiang Zhou
ZWZhi-Jun Wu
Zhi-Jun Wu
ZWZhen-Hua Wang
Zhen-Hua Wang
DYDeng-Feng Yue
Deng-Feng Yue
WYWei-Cheng Yuan
Wei-Cheng Yuan


14 January 2019 in Organic Letters
Verified
Journal Article
Closed access
JZJian-Qiang Zhao
Jian-Qiang Zhao
LYLei Yang
Lei Yang
XZXiao-Jian Zhou
Xiao-Jian Zhou
YYYong You
Yong You
ZWZhen-Hua Wang
Zhen-Hua Wang
WYWei-Cheng Yuan
Wei-Cheng Yuan

2 September 2016 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
ZWZhen-Hua Wang
Zhen-Hua Wang
ZWZhi-Jun Wu
Zhi-Jun Wu
DYDeng-Feng Yue
Deng-Feng Yue
WHWen-Fei Hu
Wen-Fei Hu
XZXiao-Mei Zhang
Xiao-Mei Zhang
WYWei-Cheng Yuan
Wei-Cheng Yuan
A highly diastereo- and enantioselective [3+2] cycloaddition reaction of N-2,2,2-trifluoroethylisatin ketimines and 3-alkenyl-5-arylfuran-2(3H)-ones was developed with 1 mol% thiourea–tertiary amine as the catalyst. A series of spiro[pyrrolidin-3,2′-oxindoles] bearing four consecutive stereocenters, including two vicinal spiro-quaternary chiral centers, were efficiently obtained with excellent results (up to >99% yield, >20 : 1 dr, and >99% ee).

12 August 2015 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
YYYong You
Yong You
ZWZhi-Jun Wu
Zhi-Jun Wu
ZWZhen-Hua Wang
Zhen-Hua Wang
XXXiao-Ying Xu
Xiao-Ying Xu
XZXiao-Mei Zhang
Xiao-Mei Zhang
WYWei-Cheng Yuan
Wei-Cheng Yuan

4 September 2015 in Chemical Communications
Verified
Journal Article
Closed access
PDF file
ZWZhen-Hua Wang
Zhen-Hua Wang
ZWZhi-Jun Wu
Zhi-Jun Wu
XHXue-Qun Huang
Xue-Qun Huang
DYDeng-Feng Yue
Deng-Feng Yue
YYYong You
Yong You
WYWei-Cheng Yuan
Wei-Cheng Yuan
The enantioselective vinylogous Michael addition of γ-substituted butenolides to 2-enoylpyridines was developed to yield γ,γ-disubstituted butenolide derivatives in excellent stereoselectivities.