Synthesis of substituted cyclohex-2-enones

M. G. Ahmed, S. A. Ahmed, U. K R Romman, K. Akhter, M. A. Chowdhury, Fumiyuki Kiuchi

研究成果: Article

2 引用 (Scopus)

抄録

Ethyl acetoacetate reacts with benzylideneacetone, 2-methoxy benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide as catalyst to yield 4-ethoxycarbonyl-3-methyl-5-phenylcyclohex-2-enone 1a, 4-ethoxycarbonyl-3-methyl-5-(2-methoxyphenyl) cyclohex-2-enone 1b and 4-ethoxycarbonyl-5-(2-furanyl)-3-methylcyclohex-2-enone 1c, respectively. Ethyl benzoylacetate reacts with benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide to give 4-ethoxycarbonyl-3,5-bis-phcnylcyclohex-2-enone 1d and 4-ethoxycarbonyl-5-(2-furanyl)-3-phenylcyclohex-2-enone 1e, respectively as products.

元の言語English
ページ(範囲)710-712
ページ数3
ジャーナルIndian Journal of Chemistry - Section B Organic and Medicinal Chemistry
40
発行部数8
出版物ステータスPublished - 2001
外部発表Yes

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Catalysts
benzylideneacetone
sodium ethoxide
ethyl acetoacetate

ASJC Scopus subject areas

  • Organic Chemistry

これを引用

Ahmed, M. G., Ahmed, S. A., Romman, U. K. R., Akhter, K., Chowdhury, M. A., & Kiuchi, F. (2001). Synthesis of substituted cyclohex-2-enones. Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 40(8), 710-712.

Synthesis of substituted cyclohex-2-enones. / Ahmed, M. G.; Ahmed, S. A.; Romman, U. K R; Akhter, K.; Chowdhury, M. A.; Kiuchi, Fumiyuki.

:: Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 巻 40, 番号 8, 2001, p. 710-712.

研究成果: Article

Ahmed, MG, Ahmed, SA, Romman, UKR, Akhter, K, Chowdhury, MA & Kiuchi, F 2001, 'Synthesis of substituted cyclohex-2-enones', Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 巻. 40, 番号 8, pp. 710-712.
Ahmed, M. G. ; Ahmed, S. A. ; Romman, U. K R ; Akhter, K. ; Chowdhury, M. A. ; Kiuchi, Fumiyuki. / Synthesis of substituted cyclohex-2-enones. :: Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 2001 ; 巻 40, 番号 8. pp. 710-712.
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abstract = "Ethyl acetoacetate reacts with benzylideneacetone, 2-methoxy benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide as catalyst to yield 4-ethoxycarbonyl-3-methyl-5-phenylcyclohex-2-enone 1a, 4-ethoxycarbonyl-3-methyl-5-(2-methoxyphenyl) cyclohex-2-enone 1b and 4-ethoxycarbonyl-5-(2-furanyl)-3-methylcyclohex-2-enone 1c, respectively. Ethyl benzoylacetate reacts with benzylideneacetone and furfurylideneacetone in the presence of sodium ethoxide to give 4-ethoxycarbonyl-3,5-bis-phcnylcyclohex-2-enone 1d and 4-ethoxycarbonyl-5-(2-furanyl)-3-phenylcyclohex-2-enone 1e, respectively as products.",
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AU - Romman, U. K R

AU - Akhter, K.

AU - Chowdhury, M. A.

AU - Kiuchi, Fumiyuki

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