Novel and Facile Syntheses of Alkenyl, Alkynyl, and Aryl 1,2-Diketones

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Abstract

Novel and facile routes to alkenyl, alkynyl, and aryl 1,2-diketones utilize treatment of benzotriazole derivatives 1, 7a,b, and 15a-d with butyllithium and subsequent reaction with esters or acid chlorides to yield the substituted intermediates 2a-d, 8a,b, and 16a-g, Reactions of the deprotonated 1 and 7 with α,β-unsaturated aldehydes followed by oxidation also produces similar intermediates 5 and 11a,b. Subsequent hydrolyses of the intermediates of type 2, 5, 8,11, and 16 afford diverse 1,2-diketones in good yields.

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Katritzky, A. R., Wang, Z., Lang, H., & Feng, D. (1997). Novel and Facile Syntheses of Alkenyl, Alkynyl, and Aryl 1,2-Diketones. Journal of Organic Chemistry, 62(12), 4125–4130. https://doi.org/10.1021/jo970092j

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