4.8 Article

Tunable Silver-Catalyzed Nitrene Transfer: From Chemoselectivity to Enantioselective C-H Amination

期刊

ACS CATALYSIS
卷 12, 期 9, 页码 5527-5539

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c01097

关键词

nitrene transfer; C-N bond formation; silver catalysis; enantioselectivity; amination; amines; aziridines; C-H functionalization

资金

  1. NSF [1664374, 1954325]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Chemistry [1954325] Funding Source: National Science Foundation
  4. Direct For Mathematical & Physical Scien
  5. Division Of Chemistry [1664374] Funding Source: National Science Foundation

向作者/读者索取更多资源

Transition-metal-catalyzed C-H aminations via nitrene transfer processes are powerful synthetic methods to construct valuable amines. Recent efforts in silver-catalyzed nitrene transfer reactions have achieved chemo-, site-, and enantioselective transformations using simple N-dentate ligands. These findings serve as a foundation for future investigations of other tunable C-H functionalizations.
Transition-metal-catalyzed C-H aminations via nitrene transfer processes are powerful synthetic methods to construct valuable amines. Over the past decade, significant efforts in the field have resulted in an expansion in the utility of nitrene transfer chemistry, enabling the use of these carbon-nitrogen bond-forming reactions in complex organic molecule syntheses. This Perspective highlights efforts in silver-catalyzed nitrene transfer reactions that achieve chemo-, site-, and enantioselective transformations using simple N-dentate ligands that can serve as stepping stones for future investigations of other tunable C-H functionalizations.

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