Highly selective C–H bond activation of N-arylbenzimidamide and divergent couplings with diazophosphonate compounds: a catalyst-controlled selective synthetic strategy for 3-phosphorylindoles and 4-phosphorylisoquinolines

2019 ◽  
Vol 6 (3) ◽  
pp. 393-398 ◽  
Author(s):  
Qiaolan Yang ◽  
Chenglin Wu ◽  
Jianhui Zhou ◽  
Guoxue He ◽  
Hong Liu ◽  
...  

A highly efficient synthetic strategy to construct 3-phosphorylindole and 4-phosphorylisoquinoline was achieved.

2015 ◽  
Vol 34 (11) ◽  
pp. 2703-2706 ◽  
Author(s):  
Benedikt S. Soller ◽  
Stephan Salzinger ◽  
Christian Jandl ◽  
Alexander Pöthig ◽  
Bernhard Rieger

RSC Advances ◽  
2015 ◽  
Vol 5 (65) ◽  
pp. 52452-52458 ◽  
Author(s):  
Xiaojia Liu ◽  
Yurong Gao ◽  
Mengxue Zhang ◽  
Xiaoyun Zhang ◽  
Suiping Wang ◽  
...  

In this work, we develop a simple and low-cost synthetic strategy to prepare fluorescent BCN hybrid nanosheets.


2021 ◽  
Author(s):  
Fangcao Zhang ◽  
Mingliang Gong ◽  
Hongzhen Xie ◽  
Yunjie Luo

Catalytic reduction of esters is a favourable synthetic strategy to obtain the corresponding alcohols. La(CH2C6H4NMe2-o)3, a simple and facilely accessible lanthanide complex, can serve as a highly efficient catalyst for...


RSC Advances ◽  
2015 ◽  
Vol 5 (42) ◽  
pp. 33595-33606 ◽  
Author(s):  
Kannan Thirumurthy ◽  
Ganesamoorthy Thirunarayanan

A facilely designed green synthetic strategy of a peony flower-like SO42−–SnO2-fly ash nano-catalyst for the synthesis of an unusual product in water.


2016 ◽  
Vol 18 (20) ◽  
pp. 5635-5642 ◽  
Author(s):  
Subhash L. Yedage ◽  
Bhalchandra M. Bhanage

In this report synthesis of isoquinolinones, isocoumarins, and N-methyl isoquinolinones and olefination of Weinreb amides by C–H bond activation using Ru(ii)/PEG-400 as green and recyclable media are documented.


Synthesis ◽  
2021 ◽  
Author(s):  
Jingwen You ◽  
Qiang Chen ◽  
Yasushi Nishihara

Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon-sulfur bonds via a highly efficient decarbonylative process.


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