A novel nickel-catalyzed synthesis of thioesters, esters and amides from aryl iodides in the presence of chromium hexacarbonyl

2015 ◽  
Vol 39 (8) ◽  
pp. 6445-6452 ◽  
Author(s):  
Nasser Iranpoor ◽  
Habib Firouzabadi ◽  
Elham Etemadi-Davan ◽  
Arash Nematollahi ◽  
Hamid Reza Firouzi

Aryl iodides undergo NiCl2-catalyzed carbon–heteroatom bond formation and carbonyl group insertion using thiol, alcohol, and amine nucleophiles with Cr(CO)6.

2020 ◽  
Vol 5 (32) ◽  
pp. 9908-9910
Author(s):  
Pu Mao ◽  
Hong‐Da Sui ◽  
Jin‐Wei Yuan ◽  
Yong‐Mei Xiao ◽  
Liang‐Ru Yang ◽  
...  

RSC Advances ◽  
2020 ◽  
Vol 10 (48) ◽  
pp. 28902-28905
Author(s):  
Xue-Yan Yang ◽  
Ruizhe Wang ◽  
Lu Wang ◽  
Jianjun Li ◽  
Shuai Mao ◽  
...  

K2S2O8-promoted C–Se bond formation from the cross-coupling of C(sp3)–H bond adjacent to carbonyl group with diphenyl diselenide under metal-free conditions.


ChemInform ◽  
2007 ◽  
Vol 38 (25) ◽  
Author(s):  
Hui Zhang ◽  
Weiguo Cao ◽  
Dawei Ma
Keyword(s):  

2007 ◽  
Vol 37 (1) ◽  
pp. 25-35 ◽  
Author(s):  
Hui Zhang ◽  
Weiguo Cao ◽  
Dawei Ma
Keyword(s):  

Synthesis ◽  
2020 ◽  
Author(s):  
Zhi-Bing Dong ◽  
Yue-Xiao Wu ◽  
Kang Peng ◽  
Jing-Hang Li

A new, efficient copper-catalyzed C(sp2)–S formation of phenyl dithiocarbamates starting from aryl iodides and tetramethylthiuram monosulfide (TMTM) was developed. The target compounds, phenyl dithiocarbamates with active sites, were synthesized smoothly in good to excellent yields. The easy performance, high yields, decent functional group compatibility, and cost-effective substrates make the protocol practical and attractive in C–S bond formation.


ChemInform ◽  
2009 ◽  
Vol 40 (10) ◽  
Author(s):  
Masakazu Sono ◽  
Takayuki Mizutani ◽  
Masayo Nozaki ◽  
Shigeru Takaoka ◽  
Motoo Tori

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