• 제목/요약/키워드: $\alpha,\beta$-Unsaturated esters

검색결과 19건 처리시간 0.02초

Organocatalytic Enantioselective Michael Addition of α-Nitroacetate to α,β-Unsaturated Enones: A Route to Chiral γ-Nitro Ketones and δ-Keto Esters

  • Moon, Hyoung-Wook;Kim, Dae-Young
    • Bulletin of the Korean Chemical Society
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    • 제32권1호
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    • pp.291-295
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    • 2011
  • The catalytic enantioselective conjugate addition reaction of $\alpha$-nitroacetate to $\alpha,\beta$-unsaturated enones promoted by chiral bifunctional organocatalysts is described. The treatment of $\alpha$-nitroacetate to $\alpha,\beta$-unsaturated enones afforded the corresponding Michael adducts with high enantioselectivity. The conjugate addition adducts are easily converted to chiral $\gamma$-nitro ketones and $\delta$-keto esters.

Selective Reduction of $\alpha,\beta$-Unsaturated Ketones with Borohydride Exchange Resin-$CuSO_4$ in Methanol

  • Yoon, Nung-Min;Sim, Tae-Bo
    • Bulletin of the Korean Chemical Society
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    • 제14권6호
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    • pp.749-752
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    • 1993
  • Borohydride exchange resin $(BER)-CuSO_4$ system readily reduces {\alpha},{\beta}$-unsaturated ketones to the corresponding saturated alcohols quantitatively. This reduction tolerates many functional groups such as carbon-carbon multiple bonds, chlorides, epoxides, esters, amides and nitriles.

Clean Reduction of $\alpha,\beta$-Unsaturated Carboxylic Acid Derviatives to the Saturated Derivatives by Potassium Triphenylborohydride in the Presence of Phenol

  • Park, Soo-Bong;Kim, Kwan-Eung;Yoon, Nung-Min
    • Bulletin of the Korean Chemical Society
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    • 제9권6호
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    • pp.352-355
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    • 1988
  • ${\alpha},{\beta}$-unsaturated carboxylic acid derivatives such as esters, amides, and nitriles are readily reduced to the corresponding saturated derivatives by potassium triphenylborohydride, $KPh_3BH$, in the presence of phenol, a quenching agent, in excellent yields.