Efficient, versatile and practical palladium-catalyzed highly regioselective ortho-halogenation of azoxybenzenes

2016 ◽  
Vol 14 (1) ◽  
pp. 323-329 ◽  
Author(s):  
Meng Sun ◽  
Xiangxiang Chen ◽  
Liang Zhang ◽  
Wei Sun ◽  
Zhe Wang ◽  
...  

A highly efficient and practical strategy of regio-selective ortho-halogenation of azoxybenzenes with NXS in the presence of palladium catalysts has been developed in good to excellent yields.

RSC Advances ◽  
2016 ◽  
Vol 6 (105) ◽  
pp. 103149-103159 ◽  
Author(s):  
Elad Meller ◽  
Yoel Sasson ◽  
Zeev Aizenshtat

Highly efficient catalytic hydrogenation of halogenated furfurals to 5-methyl furfural over activated carbon supported palladium catalysts is demonstrated.


2013 ◽  
Vol 53 (5) ◽  
pp. 1420-1424 ◽  
Author(s):  
Lin He ◽  
Haoquan Li ◽  
Helfried Neumann ◽  
Matthias Beller ◽  
Xiao-Feng Wu

2014 ◽  
Vol 126 (5) ◽  
pp. 1444-1448 ◽  
Author(s):  
Lin He ◽  
Haoquan Li ◽  
Helfried Neumann ◽  
Matthias Beller ◽  
Xiao-Feng Wu

Catalysts ◽  
2016 ◽  
Vol 6 (2) ◽  
pp. 27 ◽  
Author(s):  
Enoch Mensah ◽  
Francisco Reyes ◽  
Eric Standiford

2009 ◽  
Vol 62 (1) ◽  
pp. 27 ◽  
Author(s):  
Vaibhav P. Mehta ◽  
Sachin G. Modha ◽  
Denis Ermolat'ev ◽  
Kristof Van Hecke ◽  
Luc Van Meervelt ◽  
...  

A highly efficient method for the synthesis of diversely substituted furo[2,3-b]pyrazines has been elaborated. The Ag+- or iodine-mediated electrophilic cyclization of readily generated 5-chloro-3-substituted ethynyl-1-(4-methoxybenzyl)-pyrazin-2(1H)-ones affords substituted furo[2,3-b]pyrazines, which undergo various palladium catalyzed reactions to generate a library of difficult to attain diversely substituted furo[2,3-b]pyrazines.


Synlett ◽  
2021 ◽  
Author(s):  
Hai-Hua Lu ◽  
Meng-Yue Cao

With the introduction of new Trost-type bisphosphine ligands bearing a chiral cycloalkane framework, the highly efficient and enantioselective Palladium-catalyzed decarboxylative dearomative asymmetric allylic alkylation (AAA) of benzofurans was achieved. This enabled a diversity-oriented synthesis (DOS) of previously unreachable flavaglines, which features two diversification stages. A new avenue for developing flavagline-based drugs was thus established.


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