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Enantioselective Palladium-Catalyzed Domino Carbonylative Heck Esterification of o-Iodoalkenylbenzenes with Arylboronic Acids.
Zhang, Yao-Du; Chen, Ming; Li, Yang; Liu, Bo-Wen; Ren, Zhi-Hui; Guan, Zheng-Hui.
Afiliação
  • Zhang YD; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
  • Chen M; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
  • Li Y; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
  • Liu BW; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
  • Ren ZH; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
  • Guan ZH; Key Laboratory of Synthetic and Nature Molecule of Ministry of Education, Department of Chemistry & Materials Science, Northwest University, Xi'an 710127, P.R. China.
Org Lett ; 25(45): 8110-8115, 2023 Nov 17.
Article em En | MEDLINE | ID: mdl-37921830
The current investigation presents an innovative palladium-catalyzed asymmetric carbonylative Heck esterification method. This approach facilitates the efficient synthesis of various chiral γ-ketoacid esters by utilizing o-alkenyliodobenzenes and arylboronic acids as primary substrates. This reaction achieves the creation of three carbon-carbon bonds, two carbon-oxygen bonds, and the establishment of a quaternary carbon center within a single step. The α-chiral γ-ketoacid esters were obtained in yields ranging from good to high yields, displaying enantiomeric excesses (ee's) levels up to 92% under mild reaction conditions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article