A new three-carbon synthon for efficient synthesis of benzannelated and 1-(2-arylethenyl) heterocycles

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Abstract

The novel three-carbon synthon 1-(1H-1,2,3-benzotriazol-1-yl)-3-chloroacetone for the synthesis of benzothiazoles, pyrido[1,2-a]indoles, and styryl-substituted indolizines and imidazo[1,2-a]pyridines is reported. The proposed routes are a general and efficient approach for heterocyclizations followed by benzannelations or attachment of arylethenyl pharmacophores.

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Katritzky, A. R., Tymoshenko, D. O., Monteux, D., Vvedensky, V., Nikonov, G., Cooper, C. B., & Deshpande, M. (2000). A new three-carbon synthon for efficient synthesis of benzannelated and 1-(2-arylethenyl) heterocycles. Journal of Organic Chemistry, 65(23), 8059–8062. https://doi.org/10.1021/jo000946r

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