期刊文献+

过渡金属催化的双齿导向基辅助的惰性C(sp^3)—H键芳基化 被引量:22

Transition-Metal-Catalyzed Arylation of Unactivated C(sp^3)—H Bonds Assisted by Bidentate Directing Groups
原文传递
导出
摘要 近年来,过渡金属催化的惰性碳氢键官能团化受到广泛关注,然而,C(sp3)—H键由于低极性、高解离能和低选择性,其选择性活化尤为困难.综述了过渡金属催化的双齿导向基辅助的C(sp3)—H键芳基化的最新研究进展,主要探讨了不同过渡金属催化下芳基化反应的底物范围、反应机理和合成应用. Recently, transition-metal-catalyzed C-H functionalization has attracted tremendous interest as a valuable tool for carbon-carbon and carbon-heteroatom bond formation. However, due to the inertness of C(sp3)-H bonds and the difficulty to achieving high selectivity among the many chemically similar entities in a given molecule, the selective activation of C(sp3)-H bonds remains a great challenge. The recent progress in transition-metal-catalyzed arylation of unactivated C(sp3)-H bonds assisted by bidentate directing groups is reviewed, including the scope of reactions, mechanism and synthetic applications.
机构地区 浙江大学化学系
出处 《有机化学》 SCIE CAS CSCD 北大核心 2014年第8期1487-1498,共12页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No.J1210042) 中央高效基本科研业务费(No.2014QNA3008)资助项目~~
关键词 过渡金属 双齿导向基 C(sp3)—H键活化 芳基化 transition-metal bidentate directing group C(sp3)—H activation arylation
  • 相关文献

参考文献2

二级参考文献168

  • 1Heck, R. F.; Nolley, J. P. J. Org. Chem. 1972, 37, 2320.
  • 2Mizoroki, T.; Mori, K.; Ozaki, A. Bull. Chem. Soc. Jpn. 1971, 44, 581.
  • 3Miyaura, N.; Suzuki, A. J. Chem. Soc., Chem. Commun. 1979, 866.
  • 4Miyaura, N.; Yamada, K.; Suzuki, A. Tetrahedron Lett. 1979, 36, 3437.
  • 5Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457.
  • 6Stanforth, S. P. Tetrahedron 1998, 54, 263.
  • 7Suzuki, A. Chem. Commun. 2005, 38, 4759.
  • 8Milstein, D.; Stille, J. K. J. Am. Chem. Soc. 1978, 100, 3636.
  • 9Milstein, D.; Stille, J. K. J. Am. Chem. Soc. 1979, l O1, 4981.
  • 10Milstein, D., Stille, J. K. J. Am. Chem. Soc. 1979, 101, 4992.

共引文献14

同被引文献135

引证文献22

二级引证文献112

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