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Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines

DOI: 10.1002/asia.201301245

Source and publish data:

Chemistry - An Asian Journal p. 577 - 583 (2014)

Update date:2022-08-15

Topics:

Authors:

Ran, LongfeiRan, Longfei

Ren, Zhi-HuiRen, Zhi-Hui

Wang, Yao-YuWang, Yao-Yu

Guan, Zheng-HuiGuan, Zheng-Hui

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Article abstract of DOI:10.1002/asia.201301245

A novel and efficient palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines has been developed. The reaction tolerates a wide range of functional groups and is a reliable method for the rapid synthesis of a variety of valuable imides and tertiary benzanilides under an atmospheric pressure of CO. Copyright

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Full text of DOI:10.1002/asia.201301245

Supporting Information  
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Copyright Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2014  
Palladium-Catalyzed Aminocarbonylation of Aryl Iodides with Amides and  
N-alkyl Anilines  
[
a]  
Longfei Ran, Zhi-Hui Ren, Yao-Yu Wang, and Zheng-Hui Guan*  
asia_201301245_sm_miscellaneous_information.pdf  
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Products guided by the article

Product name:4-acetyl-N-benzoylbenzamide

Cas No:1590380-03-2

1590380-03-2

R&D Labs maybe for 1590380-03-2

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