Approach for the synthesis of N-phenylamides from β-ketobutylanilides using dimethylformamide and dimethylacetamide as the acyl donors

Joint Authors

Tan, Liquan
Zhou, Peng
Chen, Cui

Source

Journal of Saudi Chemical Society

Issue

Vol. 19, Issue 3 (30 Jun. 2015), pp.327-333, 7 p.

Publisher

Saudi Chemical Society

Publication Date

2015-06-30

Country of Publication

Saudi Arabia

No. of Pages

7

Main Subjects

Chemistry

Topics

Abstract EN

A new method including the sequence of a CAN bond formation of b-keto amides with N,N-dimethylamides and subsequently another two CAN bonds cleavage has been developed in the presence of hydrochloric acid.

The method allows us to synthesize a wide range of R-benzyl formamides and acetamides and provides a potential strategy to construct various different acyl and aryl R-phenyl amide compounds.

American Psychological Association (APA)

Chen, Cui& Tan, Liquan& Zhou, Peng. 2015. Approach for the synthesis of N-phenylamides from β-ketobutylanilides using dimethylformamide and dimethylacetamide as the acyl donors. Journal of Saudi Chemical Society،Vol. 19, no. 3, pp.327-333.
https://search.emarefa.net/detail/BIM-566505

Modern Language Association (MLA)

Chen, Cui…[et al.]. Approach for the synthesis of N-phenylamides from β-ketobutylanilides using dimethylformamide and dimethylacetamide as the acyl donors. Journal of Saudi Chemical Society Vol. 19, no. 3 (2015), pp.327-333.
https://search.emarefa.net/detail/BIM-566505

American Medical Association (AMA)

Chen, Cui& Tan, Liquan& Zhou, Peng. Approach for the synthesis of N-phenylamides from β-ketobutylanilides using dimethylformamide and dimethylacetamide as the acyl donors. Journal of Saudi Chemical Society. 2015. Vol. 19, no. 3, pp.327-333.
https://search.emarefa.net/detail/BIM-566505

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references : p. 332-333

Record ID

BIM-566505