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Conversion of Aldehydes to Branched or Linear Ketones via Regiodivergent Rhodium-Catalyzed Vinyl Bromide Reductive Coupling-Redox Isomerization Mediated by Formate.
Swyka, Robert A; Shuler, William G; Spinello, Brian J; Zhang, Wandi; Lan, Chunling; Krische, Michael J.
Afiliação
  • Swyka RA; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
  • Shuler WG; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
  • Spinello BJ; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
  • Zhang W; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
  • Lan C; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
  • Krische MJ; Department of Chemistry , University of Texas at Austin , Austin , Texas 78712 , United States.
J Am Chem Soc ; 141(17): 6864-6868, 2019 05 01.
Article em En | MEDLINE | ID: mdl-30998328
ABSTRACT
A regiodivergent catalytic method for direct conversion of aldehydes to branched or linear alkyl ketones is described. Rhodium complexes modified by P tBu2Me catalyze formate-mediated aldehyde-vinyl bromide reductive coupling-redox isomerization to form branched ketones. Use of the less strongly coordinating ligand, PPh3, promotes vinyl- to allylrhodium isomerization en route to linear ketones. This method bypasses the 3-step sequence often used to convert aldehydes to ketones involving the addition of pre-metalated reagents to Weinreb or morpholine amides.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ródio / Compostos de Vinila / Aldeídos / Complexos de Coordenação / Formiatos / Cetonas Idioma: En Revista: J Am Chem Soc Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ródio / Compostos de Vinila / Aldeídos / Complexos de Coordenação / Formiatos / Cetonas Idioma: En Revista: J Am Chem Soc Ano de publicação: 2019 Tipo de documento: Article