RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재 SCOPUS SCIE

      Visible‐light‐mediated synthesis of 3‐arylsulfonylated thioflavones using an in situ activation strategy

      한글로보기

      https://www.riss.kr/link?id=A108845223

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      We have developed a visible‐light‐mediated synthesis of 3‐arylsulfonylated thioflavones using an in situ‐activation strategy. The reaction proceeds through a one‐pot, three‐component pathway, without the need for sensitive or harsh reaction conditions. Organic photocatalysts were employed to generate aryl radicals more efficiently from aryl diazonium salts generated in situ. This method enables the synthesis of 3‐arylsulfonylated thioflavones from aryl amines and methylthiolated alkynones, utilizing potassium metabisulfite as an inexpensive source of sulfur dioxide. The resulting products were obtained under mild reaction conditions. This approach provides an efficient alternative pathway for synthesizing thioflavone derivatives, which are prevalent among various bioactive compounds.
      번역하기

      We have developed a visible‐light‐mediated synthesis of 3‐arylsulfonylated thioflavones using an in situ‐activation strategy. The reaction proceeds through a one‐pot, three‐component pathway, without the need for sensitive or harsh reactio...

      We have developed a visible‐light‐mediated synthesis of 3‐arylsulfonylated thioflavones using an in situ‐activation strategy. The reaction proceeds through a one‐pot, three‐component pathway, without the need for sensitive or harsh reaction conditions. Organic photocatalysts were employed to generate aryl radicals more efficiently from aryl diazonium salts generated in situ. This method enables the synthesis of 3‐arylsulfonylated thioflavones from aryl amines and methylthiolated alkynones, utilizing potassium metabisulfite as an inexpensive source of sulfur dioxide. The resulting products were obtained under mild reaction conditions. This approach provides an efficient alternative pathway for synthesizing thioflavone derivatives, which are prevalent among various bioactive compounds.

      더보기

      참고문헌 (Reference)

      1 R. L. Lopez de Compadre, 30 : 900-, 1987

      2 K. Tanaka, 22 : 5207-, 2020

      3 M. Artico, 43 : 1886-, 2000

      4 C. C. Chen, 17 : 736-, 2015

      5 D. Joseph, 11 : 4169-, 2021

      6 P. Prasit, 9 : 1773-, 1999

      7 M. H. Holshouser, 24 : 853-, 1981

      8 H. -K. Wang, 39 : 1975-, 1996

      9 P. Nussbaumer, 45 : 4310-, 2002

      10 J. Dong, 18 : 1714-, 2018

      1 R. L. Lopez de Compadre, 30 : 900-, 1987

      2 K. Tanaka, 22 : 5207-, 2020

      3 M. Artico, 43 : 1886-, 2000

      4 C. C. Chen, 17 : 736-, 2015

      5 D. Joseph, 11 : 4169-, 2021

      6 P. Prasit, 9 : 1773-, 1999

      7 M. H. Holshouser, 24 : 853-, 1981

      8 H. -K. Wang, 39 : 1975-, 1996

      9 P. Nussbaumer, 45 : 4310-, 2002

      10 J. Dong, 18 : 1714-, 2018

      11 S. Sangeetha, 21 : 75-, 2019

      12 X. Zheng, 2020 : 4534-, 2020

      13 A. Nohara, 18 : 34-, 1975

      14 T. Horie, 34 : 2169-, 1991

      15 F. A. A. van Acker, 43 : 3752-, 2000

      16 M. Pal, 70 : 7179-, 2005

      17 Z. -W. Feng, 44 : 14786-, 2020

      18 Y. -Q. Jiang, 362 : 2609-, 2020

      19 D. M. D’Souza, 36 : 1095-, 2007

      20 B. H. Rotstein, 114 : 8323-, 2014

      21 R. O. Rocha, 5 : 972-, 2020

      22 S. E. John, 8 : 4237-, 2021

      23 V. S. Bhat, 364 : 3088-, 2022

      24 E. J. Emmett, 4 : 602-, 2015

      25 G. Qiu, 5 : 691-, 2018

      26 B. Nguyen, 132 : 16372-, 2010

      27 H. Woolven, 13 : 4876-, 2011

      28 K. Hofman, 24 : 11852-, 2018

      29 F. -S. He, 57 : 12603-, 2021

      30 F. -S. He, 8 : 6119-, 2021

      31 X. Wang, 8 : 3308-, 2021

      32 J. A. Andrews, 54 : 1695-, 2022

      33 Q. Li, 9 : 3781-, 2022

      34 B. Qin, 9 : 3521-, 2022

      35 M. Seyed Hashtroudi, 20 : 2149-, 2022

      36 J. Zhang, 9 : 917-, 2022

      37 S. Ye, 56 : 4145-, 2020

      38 O. Fischer, 27 : 5417-, 2021

      39 J. M. R. Narayanam, 40 : 102-, 2011

      40 L. Shi, 41 : 7687-, 2012

      41 J. W. Tucker, 77 : 1617-, 2012

      42 C. K. Prier, 113 : 5322-, 2013

      43 D. M. Schultz, 343 : 1239176-, 2014

      44 S. Afewerki, 116 : 13512-, 2016

      45 N. A. Romero, 116 : 10075-, 2016

      46 K. L. Skubi, 116 : 10035-, 2016

      47 B. König, 2017 : 1979-, 2017

      48 C. -S. Wang, 118 : 7532-, 2018

      49 P. Das, 17 : e202200085-, 2022

      50 G. C. Upreti, 7 : 29728-, 2022

      51 K. Fidaly, 14 : 1293-, 2012

      52 A. Srivastava, 10 : 39495-, 2020

      53 한순규, "“K-synthesis”: Recent advancements in natural product synthesis enabled by unique methods and strategies development in Korea" 대한화학회 44 (44): 172-201, 2023

      더보기

      동일학술지(권/호) 다른 논문

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼