4.7 Article

Palladium-Nanoparticle-Catalyzed 1,7-Palladium Migration Involving C-H Activation, Followed by Intramolecular Amination: Regioselective Synthesis of N1-Arylbenzotriazoles and an Evaluation of Their Inhibitory Activity toward Indoleamine 2,3-Dioxygenase

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 79, Issue 13, Pages 6366-6371

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo5009838

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan (MEXT)
  2. Grants-in-Aid for Scientific Research [26288051, 23246013, 25105702, 25670049] Funding Source: KAKEN

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A sulfur-modified gold-supported palladium material (SAPd) has been developed bearing palladium nanoparticles on its surface. Herein, we report for the first time the use of SAPd to affect a Pd-nanoparticle-catalyzed 1,7-Pd migration reaction for the synthesis of benzotriazoles via C-H bond activation. The resulting benzotriazoles were evaluated in terms of their inhibitory activity toward indoleamine 2,3-dioxygenase.

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