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    DMSO 용매를 활용한 퀴놀론의 친환경적인 합성법 개발

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    https://www.riss.kr/link?id=T16950946

    • 저자
    • 발행사항

      청주 : 충북대학교, 2024

    • 학위논문사항

      학위논문(석사) -- 충북대학교 , 신약개발전공 , 2024. 2

    • 발행연도

      2024

    • 작성언어

      한국어

    • KDC

      518.44 판사항(5)

    • 발행국(도시)

      충청북도

    • 기타서명

      Using DMSO Solvent

    • 형태사항

      v, 63p. ; 26 cm

    • 일반주기명

      충북대학교 논문은 저작권에 의해 보호됩니다
      지도교수:정재경
      참고문헌: p.35-37

    • UCI식별코드

      I804:43009-000000059560

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      • 충북대학교 도서관 소장기관정보
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    부가정보

    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    Quinolone motifs are widespread in various biologically active natural and pharmaceutical compounds. Previously, a reagent-free synthesis of flavones from o-alkynoylphenols has been developed with DMSO promotion. In this regard, o-alkynoyl aniline was tested, and both 5-exo and 6-endo cyclized rings were observed. The conditions were slightly modified, and quinolones were successfully achieved via 6-endo cyclization. The developed method tolerates various functional groups and yields the corresponding quinolones. A reagent- free, operationally simple, highly atom-economic, environmentally benign, and mild- conditioned method has been developed for synthesizing quinolones. This method will be useful for the synthesis of biologically active compounds, including 4-quimolone motif structure. * A thesis for the degree of Master of science in Pharmacy in February 2024
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    Quinolone motifs are widespread in various biologically active natural and pharmaceutical compounds. Previously, a reagent-free synthesis of flavones from o-alkynoylphenols has been developed with DMSO promotion. In this regard, o-alkynoyl aniline was...

    Quinolone motifs are widespread in various biologically active natural and pharmaceutical compounds. Previously, a reagent-free synthesis of flavones from o-alkynoylphenols has been developed with DMSO promotion. In this regard, o-alkynoyl aniline was tested, and both 5-exo and 6-endo cyclized rings were observed. The conditions were slightly modified, and quinolones were successfully achieved via 6-endo cyclization. The developed method tolerates various functional groups and yields the corresponding quinolones. A reagent- free, operationally simple, highly atom-economic, environmentally benign, and mild- conditioned method has been developed for synthesizing quinolones. This method will be useful for the synthesis of biologically active compounds, including 4-quimolone motif structure. * A thesis for the degree of Master of science in Pharmacy in February 2024

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    목차 (Table of Contents)

    • List of Figures ii
    • List of Tables . ii
    • List of Schemes ii
    • List of Abbreviations iii
    • Abstract v
    • List of Figures ii
    • List of Tables . ii
    • List of Schemes ii
    • List of Abbreviations iii
    • Abstract v
    • Ⅰ. 서 론 1
    • Ⅱ. 본 론 5
    • 1. 합성 설계 . 5
    • 2. 합성. 8
    • Ⅲ. 결 론 17
    • Ⅳ. 실 험 18
    • 1. 측정기기 및 시약 .18
    • 2. 합성 방법 19
    • Ⅴ. 참고 문헌 35
    • Ⅵ. 부 록 38
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