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Note | Regular issue | Vol 63, No. 7, 2004, pp.1659-1665
Published online, 11th May, 2004
DOI: 10.3987/COM-04-10085
Chemical Behavior of 3,5-Dicyanoisoxazoles

Mina Tamura, Tae Nishimura, Nagatoshi Nishiwaki,* and Masahiro Ariga*

*Department of Chemistry, Osaka Kyoiku University, 4-698-1 Asahigaoka, Kashiwara, Osaka 582-8582, Japan

Abstract

Cyano groups on 3,5-dicyanoisoxazole readily caused nucleophilic addition of alcohols (or amines) to give corresponding imidates (or amidines). Dicyanoisoxazoles was also converted to 3,5-bis(imidazolinyl)isoxazoles upon treatment with 1,2-diamines.