3899-92-1Relevant articles and documents
Synthesis, anti-oomycete activity, and SAR studies of paeonol derivatives
Tian, Yue-E,Sun, Di,Han, Xiao-Xiao,Yang, Jin-Ming,Zhang, Song,Feng, Nan-Nan,Zhu, Li-Na,Xu, Zhong-Yuan,Che, Zhi-Ping,Liu, Sheng-Ming,Lin, Xiao-Min,Jiang, Jia,Chen, Gen-Qiang
, p. 138 - 149 (2020/02/11)
Three series of sulfonate derivatives of paeonol were synthesized and screened in?vitro for their anti-oomycete activity against P. capsici, respectively. Among all the compounds, 4m displayed the best promising and pronounced anti-oomycete activity again
Coupling of C(sp3)-H bonds with C(sp2)-O electrophiles: mild, general and selective
Gui, Yong-Yuan,Liao, Li-Li,Sun, Liang,Zhang, Zhen,Ye, Jian-Heng,Shen, Guo,Lu, Zhi-Peng,Zhou, Wen-Jun,Yu, Da-Gang
supporting information, p. 1192 - 1195 (2017/02/05)
Herein is reported the mild and general coupling of amine/ether C(sp3)-H bonds with various kinds of C(sp2)-O electrophiles with high selectivity and efficiency. Valuable allylic/benzylic amines are generated in moderate to excellent yields. The utility of this transformation is demonstrated by a broad substrate scope (>50 examples), good functional group tolerance and facile product modification.
Nickel-catalyzed C-P coupling of aryl mesylates and tosylates with H(O)PR1R2
Shen, Chaoren,Yang, Guoqiang,Zhang, Wanbin
supporting information; body text, p. 3500 - 3505 (2012/05/20)
A method was developed for the nickel-catalyzed phosphonylation of aryl mesylates and tosylates with H(O)PR1R2. To the best of our knowledge, this is the first example of nickel-catalyzed C-P coupling of aryl mesylates and tosylates. Most of the substrates gave moderate to good yields under our catalytic system.
