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      "Studies on the Reactivity, Synthesis and Mechanism of Heterocyclic Compounds" = "헤테로고리 화합물의 반응성, 합성및 메카니즘에 관한 연구"

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      https://www.riss.kr/link?id=E688750

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      다국어 초록 (Multilingual Abstract)

      A stable sulfone derivative of 2,4,6-trinethylcyclohexa-2,4-diene-1-one (7) undergoes faring cleavage under visible highest to produce a ketene intermediate, which could be efficiency captured by amines to give amides even in the presence of competing nucleophiles such as water and ethanol.
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      A stable sulfone derivative of 2,4,6-trinethylcyclohexa-2,4-diene-1-one (7) undergoes faring cleavage under visible highest to produce a ketene intermediate, which could be efficiency captured by amines to give amides even in the presence of competing...

      A stable sulfone derivative of 2,4,6-trinethylcyclohexa-2,4-diene-1-one (7) undergoes faring cleavage under visible highest to produce a ketene intermediate, which could be efficiency captured by amines to give amides even in the presence of competing nucleophiles such as water and ethanol.

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      목차 (Table of Contents)

      • Rearrangements and Aromatization of Tetramethyl 3a,7a-Dihydroindole-2,3,3a,4-tetracarboxylates
      • Abstract
      • Results and Discussion
      • Experimental Section
      • Rearrangements and Aromatization of Tetramethyl 3a,7a-Dihydroindole-2,3,3a,4-tetracarboxylates
      • Abstract
      • Results and Discussion
      • Experimental Section
      • References
      • Synthesis of Facially Encumbered Porphyrins and Partially Deuterated Porphyrins
      • Summary
      • Ⅰ. 서 론
      • Ⅱ. 실 험
      • Ⅲ. 결과 및 고찰
      • Ⅳ. 결론
      • Ⅴ. 참고문헌
      • Reaction of 3-Trimethylsilyl-2-propargylzinc Bromide with Cyclic Imides:
      • Abstract
      • References and Notes
      • A Facile Synthesis of 7 ,7-Dimethyl-6,8-dioxabicyclo[3,2,1]octane, A Constituent of the Japanese Hop Oil, Humulus Lupulus
      • References
      • The Tightness Contribution to the BrΦnsted a for Hydride Transfer between NAD+ Analogyes
      • between NAD + Analogues
      • 1. Introduction
      • 2. Experimental
      • 3. Potential Surfaces
      • 4. Results and Discussion
      • 5. Conclusion
      • References and Footnotes
      • Synthesis of Five-membered 2-Heteroaryl 2-Heteroaromatic Carboxylates and Attempted Cyclization to Bisheteroary[2, 3-b, 3¹,2¹-d] pyran-2-one
      • Experimental
      • References and Footnotes
      • SmI2 -Induced Ring Expansion Reactions of Alkyl (n+1)-Oxyobicyclo[n.1.0]alkane-1-carboxylates
      • Abstract
      • References
      • Reactivities of Five-Membered Heterocycles in Hydride Transfer Reactions
      • Introduction
      • Marcus Theory
      • Experimental Section
      • Discussion
      • Preparation of ω-Tetrahydropyran-2-ylsulfanylalkylniaginesium Chlorides: Useful Reagents for the Synthesis of l-(ω-Mercaptoalkyl)-l
      • tlihydrobuckminsterfullerenes (C60 )
      • Abstract
      • References and Notes
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