Palladium-catalysed cross-coupling reactions of aryl-, alkenyl- and alkynyl-iodonium salts and iodanes with terminal alkynes in aqueous medium

1996 ◽  
pp. 835 ◽  
Author(s):  
Suk-Ku Kang ◽  
Hong-Woo Lee ◽  
Su-Bum Jang ◽  
Pil-Su Ho
Author(s):  
Varshini Jayantha Kumar ◽  
Jian-Zhong Wu ◽  
Martyna Judd ◽  
Elodie ROUSSET ◽  
Marcus Korb ◽  
...  

A series of 6-oxo verdazyl radicals functionalised at the 1- and 5-positions by methyl, thiomethyl and iodo groups were synthesised using conventional strategies. Facile Sonogashira cross-coupling reactions of terminal alkynes...


2014 ◽  
Vol 12 (32) ◽  
pp. 6215-6222 ◽  
Author(s):  
Tiebo Xiao ◽  
Ping Zhang ◽  
Yang Xie ◽  
Jun Wang ◽  
Lei Zhou

A general source of dialkoxycarbenes, 2,2-dialkoxy-5,5-dimethyl-Δ3-1,3,4-oxadiazolines, have been successfully employed as coupling partners in CuI-catalyzed cross-coupling reactions with terminal alkynes, which afforded various unsymmetrical propargylic acetals in good yields.


RSC Advances ◽  
2016 ◽  
Vol 6 (111) ◽  
pp. 109296-109300 ◽  
Author(s):  
Xian Wang ◽  
Zhenhua Wang ◽  
Zunyuan Xie ◽  
Guofang Zhang ◽  
Weiqiang Zhang ◽  
...  

1,3-Yones as σ-, π-electron donating ligands significantly accelerated the cross-coupling reactions of aryl iodides with terminal alkynes, in which as low as 0.1 to 1 mol% of CuI were efficiently activated.


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