Oxidative Annulations Involving DMSO and Formamide: K2S2O8 Mediated Syntheses of Quinolines and Pyrimidines
Santosh D. Jadhav and Anand Singh*
*Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur-208016, U.P. India, Email: anandsiitk.ac.in
S. D. Jadhav, A. Singh, Org. Lett., 2017, 19, 5673-5676.
DOI: 10.1021/acs.orglett.7b02838 (free Supporting Information)
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An oxidative annulation involving anilines, aryl ketones, and DMSO as a methine (=CH−) equivalent promoted by K2S2O8 provides 4-arylquinolines, whereas activation of acetophenone-formamide conjugates enables the synthesis of 4-arylpyrimidines.
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