Palladium-catalyzed unstrained C(sp3)―N bond activation: the synthesis ofN,N-dimethylacetamide by carbonylation of trimethylamine-Reference-Cited by-同舟云学术

Palladium-catalyzed unstrained C(sp3)―N bond activation: the synthesis ofN,N-dimethylacetamide by carbonylation of trimethylamine

Published:2013-02-26 Issue:3 Volume:27 Page:177-183
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Appl. Organometal. Chem.

Author:

Mei Hui¹,Han Wenjia¹,Hu Jianglin¹,Xiao Se¹,Lei Yizhu¹,Zhang Rui¹,Mo Wanlin¹,Li Guangxing¹

Affiliation:

1. Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering; Huazhong University of Science and Technology; Wuhan; 430074; People's Republic of China

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Reference58 articles.

1. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions

2. Recent advances in the Heck–Matsuda reaction in heterocyclic chemistry

3. Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence

4. Nickel-induced conversion of carbon–nitrogen into carbon–carbon bonds. One-step transformations of aryl, quaternary ammonium salts into alkylarenes and biaryls

5. The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts

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