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Catalytic Olefin Transpositions Facilitated by Ruthenium N,N,N-Pincer Complexes.
Davies, Alex M; Greene, Kara H; Allen, Anthony R; Farris, Benjamin M; Szymczak, Nathaniel K; Stephenson, Corey R J.
Afiliação
  • Davies AM; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Greene KH; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Allen AR; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Farris BM; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Szymczak NK; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Stephenson CRJ; Willard Henry Dow Laboratory, Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
J Org Chem ; 89(13): 9647-9653, 2024 Jul 05.
Article em En | MEDLINE | ID: mdl-38901003
ABSTRACT
In this report, we demonstrate olefin transposition/isomerization reactions catalyzed by a series of N,N,N-pincer (1,3-bis(2-pyridylimino)isoindoline) Ru-hydride complexes. The protocol proceeds at room temperature for most substrates, achieving excellent yields, regioselectivity, and diastereoselectivity in short reaction times. The air-stable Ru-chloride derivatives of these complexes exhibit comparable reactivity enabling benchtop setup and synthetic versatility. Furthermore, we demonstrate the potential for one-pot cascade sequences of the products derived from the transposition reactions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article