2005
DOI: 10.1002/chin.200528147
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Synthesis of Substituted and Unsubstituted 2,4‐Diaryl‐5‐oxo‐5,6,7,8‐tetrahydro‐2‐chromens.

Abstract: Benzopyran derivatives R 0350 Synthesis of Substituted and Unsubstituted 2,4-Diaryl-5-oxo-5,6,7,8-tetrahydro-2-chromens. -[via Zn(II)-mediated condensation of arylideneacetophenones (II) with cyclohexanediones (I)]. -(AHMED*, M. G.; AHMED, S. A.; ROMMAN, U. K. R.; TOUCHY, A. S.; BADAL, M. R.; HOSSAIN, M. A.; UDDIN, M. K.; Indian J.

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“…Reaction of 1 with cyclohexane-1,3-diones produced 2,4-diaryl-5-oxo-5,6,7,8tetrahydro-2-chromenes 13a, b. [53] Similarly, acetoacetanilide and acetylacetone reacted with chalcones 1 to afford cyclohexenone derivatives 14 and 15, respectively [49] (Scheme 3). Epoxidation of chalcones 1 with urea-hydrogen peroxide (UHP) under ultrasound irradiation gave oxirane derivatives 16 [54] (Scheme 3).…”
Section: Reactivity Of Chalcone Derivativesmentioning
confidence: 99%
“…Reaction of 1 with cyclohexane-1,3-diones produced 2,4-diaryl-5-oxo-5,6,7,8tetrahydro-2-chromenes 13a, b. [53] Similarly, acetoacetanilide and acetylacetone reacted with chalcones 1 to afford cyclohexenone derivatives 14 and 15, respectively [49] (Scheme 3). Epoxidation of chalcones 1 with urea-hydrogen peroxide (UHP) under ultrasound irradiation gave oxirane derivatives 16 [54] (Scheme 3).…”
Section: Reactivity Of Chalcone Derivativesmentioning
confidence: 99%