Visible-Light-Induced Nitrogen-Centered Radical Process for the Construction of 3-Acylcoumarins

Author(s):  
Quan Zhou ◽  
Fang-Ting Xiong ◽  
Pu Chen ◽  
Biquan Xiong ◽  
Kewen Tang ◽  
...  

A nitrogen-centered radical-mediated strategy is described to synthesize functionalized 3-acylcoumarins. This process is enabled by visible-light-induced acylation/cyclization reactions of alkynoates with various acyl oxime compounds in acetonitrile. The difunctionalization of...

2019 ◽  
Vol 21 (9) ◽  
pp. 3086-3092 ◽  
Author(s):  
Peng Ji ◽  
Yueteng Zhang ◽  
Yongyi Wei ◽  
He Huang ◽  
Wenbo Hu ◽  
...  

2017 ◽  
Vol 53 (69) ◽  
pp. 9644-9647 ◽  
Author(s):  
Hongyu Wang ◽  
Yanfei Ren ◽  
Kaiye Wang ◽  
Yunquan Man ◽  
Yanan Xiang ◽  
...  

1,2,4-Triazolines and 1,2,4-triazoles can be synthesized under visible light in one step without additional operations, which can be also scaled up to a gram-level.


2019 ◽  
Vol 55 (19) ◽  
pp. 2833-2836 ◽  
Author(s):  
Thurpu Raghavender Reddy ◽  
Dodla Sivanageswara Rao ◽  
Sudhir Kashyap

An unprecedented visible-light inspired selective radical azidation of unactivated and diverse substituted vinylarenes with sulfonium iodate reagent has been realized. The intrinsic radical process triggered by light tolerated several synthetically useful functionalities enabling two new carbon-hetero bonds which display distinctive late-stage applications to biologically relevant scaffolds.


2020 ◽  
Vol 18 (30) ◽  
pp. 5918-5926 ◽  
Author(s):  
Meng-Yue Wang ◽  
Xue-Qing Zhu ◽  
Xing-Long Zhang ◽  
Rui-Li Guo ◽  
Qiong Jia ◽  
...  

An unprecedented visible light-promoted approach to the synthesis of trifluoromethylthioesters from aldehydes has been developed.


2019 ◽  
Vol 10 (21) ◽  
pp. 5484-5488 ◽  
Author(s):  
Sara Cuadros ◽  
Matthew A. Horwitz ◽  
Bertrand Schweitzer-Chaput ◽  
Paolo Melchiorre

A three-component radical process is reported that, by coupling alkyl chlorides, maleimides, and heteroaromatic fragments, installs multiple biologically relevant heterocycles within complex cascade products. This method, which generates radicals via an SN2-based photochemical catalytic mechanism, activates substrates incompatible with or inert to classical radical-generating strategies.


ChemInform ◽  
2011 ◽  
Vol 42 (47) ◽  
pp. no-no
Author(s):  
Jun Xuan ◽  
Ying Cheng ◽  
Jing An ◽  
Liang-Qiu Lu ◽  
Xiao-Xiao Zhang ◽  
...  

2021 ◽  
Author(s):  
Xiao-Yu Zhang ◽  
Chao Ning ◽  
Ben Mao ◽  
Yin Wei ◽  
Min Shi

Classical cyclopropylcarbinyl radical clock reactions have been widely applied to conduct the mechanistic studies on probing radical process for a long time; however, alkylidenecyclopropanes, which have a similar molecular structure...


ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Jacob Davies ◽  
Samuel G. Booth ◽  
Stephanie Essafi ◽  
Robert A. W. Dryfe ◽  
Daniele Leonori

ACS Catalysis ◽  
2017 ◽  
Vol 7 (6) ◽  
pp. 4093-4099 ◽  
Author(s):  
Yuliang Liu ◽  
Bin Wang ◽  
Xiaofeng Qiao ◽  
Chen-Ho Tung ◽  
Yifeng Wang

Sign in / Sign up

Export Citation Format

Share Document