Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: A facile access to polysubstitution imidazoles

Cheng Kou Liu, Zhao Yang, Yu Zeng, Kai Guo, Zheng Fang, Bo Li

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

A practical, economic and efficient sodium nitrite-promoted aerobic oxidative synthesis of polysubstitution imidazoles from aryl methyl ketones has been developed. (4 or 5)-Aryl-2-aroyl-imidazoles are generated in good yields under metal-free conditions and in a one step process, which show highly potent antiproliferative activity. Based on some control experiments, a possible mechanism was proposed. Moreover, other multisubstituted heterocyclic derivatives, such as 1,2,4-trisubstituted imidazoles, were prepared under the sodium nitrite-promoted aerobic oxidative conditions.

Original languageEnglish
Pages (from-to)1508-1512
Number of pages5
JournalOrganic Chemistry Frontiers
Volume4
Issue number8
DOIs
StatePublished - Aug 2017

Fingerprint

Dive into the research topics of 'Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: A facile access to polysubstitution imidazoles'. Together they form a unique fingerprint.

Cite this