4.7 Article

PMes3-Promoted Ruthenium-Catalyzed Meta C-H Nitration of 6-Arylpurines

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 83, Issue 6, Pages 3245-3251

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.8b00149

Keywords

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Funding

  1. Chinese NSF [81773565, 81430080]
  2. National Program on Key Basic Research Project of China [2015CB910603]
  3. International Cooperative Program [GJHZ1622]
  4. Key Program of the Frontier Science of the Chinese Academy of Sciences [QYZDJ-SSW-SMC002]
  5. Shanghai Commission of Science and Technology [16XD1404600]
  6. Chinese NSF [81773565, 81430080]
  7. National Program on Key Basic Research Project of China [2015CB910603]
  8. International Cooperative Program [GJHZ1622]
  9. Key Program of the Frontier Science of the Chinese Academy of Sciences [QYZDJ-SSW-SMC002]
  10. Shanghai Commission of Science and Technology [16XD1404600]

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[Graphics] To address the challenge of meta nitration of 6-arylpurine substrates, a versatile ruthenium catalyzed meta C-H nitration is developed. The use of a sterically hindered phosphine ligand is crucial for the catalytic efficiency, and a broad class of 6-arylpurines and nucleosides were found suitable for this process providing corresponding exclusively meta nitrated products in good yields.

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