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N-Ammonium Ylide Mediators for Electrochemical C-H Oxidation.
Saito, Masato; Kawamata, Yu; Meanwell, Michael; Navratil, Rafael; Chiodi, Debora; Carlson, Ethan; Hu, Pengfei; Chen, Longrui; Udyavara, Sagar; Kingston, Cian; Tanwar, Mayank; Tyagi, Sameer; McKillican, Bruce P; Gichinga, Moses G; Schmidt, Michael A; Eastgate, Martin D; Lamberto, Massimiliano; He, Chi; Tang, Tianhua; Malapit, Christian A; Sigman, Matthew S; Minteer, Shelley D; Neurock, Matthew; Baran, Phil S.
Afiliación
  • Saito M; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Kawamata Y; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Meanwell M; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Navratil R; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Chiodi D; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Carlson E; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Hu P; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Chen L; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Udyavara S; Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Kingston C; Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
  • Tanwar M; Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Tyagi S; Product Metabolism and Analytical Science, Syngenta Crop Protection, 410 Swing Road, Greensboro, North Carolina 27409, United States.
  • McKillican BP; Product Metabolism and Analytical Science, Syngenta Crop Protection, 410 Swing Road, Greensboro, North Carolina 27409, United States.
  • Gichinga MG; Product Metabolism and Analytical Science, Syngenta Crop Protection, 410 Swing Road, Greensboro, North Carolina 27409, United States.
  • Schmidt MA; Chemical Process Development, Bristol Myers Squibb, New Brunswick, New Jersey 08903, United States.
  • Eastgate MD; Chemical Process Development, Bristol Myers Squibb, New Brunswick, New Jersey 08903, United States.
  • Lamberto M; Department of Chemistry & Physics, Monmouth University, West Long Branch, New Jersey 07740, United States.
  • He C; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Tang T; Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
  • Malapit CA; Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
  • Sigman MS; Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
  • Minteer SD; Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
  • Neurock M; Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Baran PS; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
J Am Chem Soc ; 143(20): 7859-7867, 2021 05 26.
Article en En | MEDLINE | ID: mdl-33983721
ABSTRACT
The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Técnicas Electroquímicas / Compuestos de Amonio Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Técnicas Electroquímicas / Compuestos de Amonio Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article