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Catalyst-Controlled and Tunable, Chemoselective Silver-Catalyzed Intermolecular Nitrene Transfer: Experimental and Computational Studies.
Dolan, Nicholas S; Scamp, Ryan J; Yang, Tzuhsiung; Berry, John F; Schomaker, Jennifer M.
Afiliação
  • Dolan NS; Department of Chemistry, University of Wisconsin , Madison, Wisconsin 53706, United States.
  • Scamp RJ; Department of Chemistry, University of Wisconsin , Madison, Wisconsin 53706, United States.
  • Yang T; Department of Chemistry, University of Wisconsin , Madison, Wisconsin 53706, United States.
  • Berry JF; Department of Chemistry, University of Wisconsin , Madison, Wisconsin 53706, United States.
  • Schomaker JM; Department of Chemistry, University of Wisconsin , Madison, Wisconsin 53706, United States.
J Am Chem Soc ; 138(44): 14658-14667, 2016 11 09.
Article em En | MEDLINE | ID: mdl-27726353
ABSTRACT
The development of new catalysts for selective nitrene transfer is a continuing area of interest. In particular, the ability to control the chemoselectivity of intermolecular reactions in the presence of multiple reactive sites has been a long-standing challenge in the field. In this paper, we demonstrate examples of silver-catalyzed, nondirected, intermolecular nitrene transfer reactions that are both chemoselective and flexible for aziridination or C-H insertion, depending on the choice of ligand. Experimental probes present a puzzling picture of the mechanistic details of the pathways mediated by [(tBu3tpy)AgOTf]2 and (tpa)AgOTf. Computational studies elucidate these subtleties and provide guidance for the future development of new catalysts exhibiting improved tunability in group transfer reactions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prata / Simulação por Computador / Iminas Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prata / Simulação por Computador / Iminas Idioma: En Ano de publicação: 2016 Tipo de documento: Article