期刊文献+

可见光诱导重氮化合物产生卡宾及其官能化反应 被引量:6

Visible Light-Promoted Transformation of Diazo Compounds via the Formation of Free Carbene as Key Intermediate
原文传递
导出
摘要 卡宾是有机合成中的重要中间体.在过去的几十年中,过渡金属催化的卡宾转移反应取得了显著发展.近年来,可见光促进的重氮化合物通过游离态卡宾的转化也开始兴起.该类反应仅需要使用可见光作为唯一能源,符合绿色化学理念.自2018年Davies课题组和周磊课题组分别独立报道了芳基重氮酯在可见光照射下光解生成游离态卡宾物种以来,光促重氮化合物的转化反应受到了越来越多科研工作者的关注,也催生了许多绿色高效的有机合成新反应.在前人工作基础上,进一步完善了该领域的最新进展,综述了近期可见光照射下重氮化合物的新转化反应和国内学者的贡献,展望了该领域的未来发展方向和所面临的挑战. Carbene is one of the most important synthetic intermediates in organic synthesis. In the past few decades,transition-metal catalyzed carbene transfer reactions have made remarkable development. Recently, visible light-promoted transformation of diazo compounds through the formation of free carbene as key intermediate begun to rise. The reaction only need visible light as the sole energy source which meets the concept of green chemistry. Since the pioneering works developed by the groups of Diaves and Zhou, photo-promoted transformation of diazo compounds has attracted more and more attentions.On the basis of previous work, the latest progress in this field is further improved, which mainly focuses on the recent new transformation reactions of diazo compounds under visible light irradiation and the contributions reported from Chinese research group. The future development direction, as well as challenges in this field is prospected.
作者 蔡宝贵 宣俊 Baogui Cai;Jun Xuan(Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials,College of Chemistry&Chemical Engineering,Anhui University,Hefei 230601)
出处 《有机化学》 SCIE CAS CSCD 北大核心 2021年第12期4565-4574,共10页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(Nos.21971001,21702001)资助项目。
关键词 可见光 重氮化合物 卡宾 绿色化学 visible light diazo compound carbene green chemistry
  • 相关文献

参考文献3

二级参考文献39

  • 1高金山,边庆花,郭洪超,王敏.手性金属配合物催化的不对称环丙烷化反应的新进展[J].有机化学,2007,27(4):438-448. 被引量:6
  • 2Doyle, M. P. Chem. Rev. 1986. 66. 919.
  • 3Yates, P. J. Am. Chem. Soc. 1952, 74, 5376.
  • 4Dai, X.; Warren, T. H. J. Am. Chem. Soc. 2004, 126, 10085.
  • 5Qu, Z.; Shi, W.; Wang, J. J. Org. Chem. 2001, 66, 8139.
  • 6Doyle, M. P.; McKervey, M. A.; Ye, T. Modern Catalytic methods for Organic Synthesis with Dizo Compounds, Wiley-Interscience, New York, 1998.
  • 7Denmark, S. E.; Stavenger, R. A.; Faucher, A. M.; Edwards, J. P. J. Org. Chem. 1997, 62, 3375.
  • 8Ortufio, R. M.; Ibarzo, J. Tetrahedron Lett. 1996, 37, 4059.
  • 9Rodriguez-Garcia, C.; lbarzo, J.; Alvarez-Larena, A.; Branchadell, V.; Branchadell, V.; Oliva,A; Ortuno, R. M. Tetrahedron 2001, 57, 1025.
  • 10Miller, K. J.; Baag, J. H.; Abu-Omar, M. M. Inorg. Chem. 1999, 38, 4510.

共引文献19

同被引文献47

引证文献6

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部