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Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications.
Kawamata, Yu; Vantourout, Julien C; Hickey, David P; Bai, Peng; Chen, Longrui; Hou, Qinglong; Qiao, Wenhua; Barman, Koushik; Edwards, Martin A; Garrido-Castro, Alberto F; deGruyter, Justine N; Nakamura, Hugh; Knouse, Kyle; Qin, Chuanguang; Clay, Khalyd J; Bao, Denghui; Li, Chao; Starr, Jeremy T; Garcia-Irizarry, Carmen; Sach, Neal; White, Henry S; Neurock, Matthew; Minteer, Shelley D; Baran, Phil S.
Affiliation
  • Kawamata Y; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Vantourout JC; Center for Synthetic Organic Electrochemistry , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Hickey DP; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Bai P; Department of Chemistry , University of Utah , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Chen L; Center for Synthetic Organic Electrochemistry , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Hou Q; Department of Chemical Engineering and Materials Science , University of Minnesota , Minneapolis , Minnesota 55455 , United States.
  • Qiao W; Center for Synthetic Organic Electrochemistry , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Barman K; Asymchem Life Science (Tianjin) , Tianjin Economic-Technological Development Zone, Tianjin 300457 , China.
  • Edwards MA; Asymchem Life Science (Tianjin) , Tianjin Economic-Technological Development Zone, Tianjin 300457 , China.
  • Garrido-Castro AF; Asymchem Life Science (Tianjin) , Tianjin Economic-Technological Development Zone, Tianjin 300457 , China.
  • deGruyter JN; Department of Chemistry , University of Utah , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Nakamura H; Center for Synthetic Organic Electrochemistry , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Knouse K; Department of Chemistry , University of Utah , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Qin C; Center for Synthetic Organic Electrochemistry , 315 South 1400 East , Salt Lake City , Utah 84112 , United States.
  • Clay KJ; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Bao D; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Li C; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Starr JT; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Garcia-Irizarry C; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Sach N; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • White HS; Asymchem Life Science (Tianjin) , Tianjin Economic-Technological Development Zone, Tianjin 300457 , China.
  • Neurock M; Department of Chemistry , The Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.
  • Minteer SD; Discovery Sciences, Medicine Design , Pfizer Global Research and Development , 445 Eastern Point Road , Groton , Connecticut 06340 , United States.
  • Baran PS; Discovery Sciences, Medicine Design , Pfizer Global Research and Development , 445 Eastern Point Road , Groton , Connecticut 06340 , United States.
J Am Chem Soc ; 141(15): 6392-6402, 2019 04 17.
Article in En | MEDLINE | ID: mdl-30905151
ABSTRACT
C-N cross-coupling is one of the most valuable and widespread transformations in organic synthesis. Largely dominated by Pd- and Cu-based catalytic systems, it has proven to be a staple transformation for those in both academia and industry. The current study presents the development and mechanistic understanding of an electrochemically driven, Ni-catalyzed method for achieving this reaction of high strategic importance. Through a series of electrochemical, computational, kinetic, and empirical experiments, the key mechanistic features of this reaction have been unraveled, leading to a second generation set of conditions that is applicable to a broad range of aryl halides and amine nucleophiles including complex examples on oligopeptides, medicinally relevant heterocycles, natural products, and sugars. Full disclosure of the current limitations and procedures for both batch and flow scale-ups (100 g) are also described.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electrochemical Techniques / Amines Language: En Journal: J Am Chem Soc Year: 2019 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electrochemical Techniques / Amines Language: En Journal: J Am Chem Soc Year: 2019 Type: Article Affiliation country: United States