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Asymmetric α-allylic allenylation of ß-ketocarbonyls and aldehydes by synergistic Pd/chiral primary amine catalysis.
You, Chang; Shi, Mingying; Mi, Xueling; Luo, Sanzhong.
Afiliação
  • You C; Center of Basic Molecular Science, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
  • Shi M; College of Chemistry, Beijing Normal University, Beijing, 100875, China.
  • Mi X; College of Chemistry, Beijing Normal University, Beijing, 100875, China. xlmi@bnu.edu.cn.
  • Luo S; Center of Basic Molecular Science, Department of Chemistry, Tsinghua University, Beijing, 100084, China. luosz@tsinghua.edu.cn.
Nat Commun ; 14(1): 2911, 2023 May 22.
Article em En | MEDLINE | ID: mdl-37217465
ABSTRACT
We herein describe an asymmetric α-allylic allenylation of ß-ketocarbonyls and aldehydes with 1,3-enynes. A synergistic chiral primary amine/Pd catalyst was identified to facilitate the utilization of 1,3-enynes as atom-economic and achiral allene precursors. The synergistic catalysis enables the construction of all-carbon quaternary centers-tethered allenes bearing non-adjacent 1,3-axial central stereogenic centers in high level of diastereo- and enantio-selectivity. By switching the configurations of ligands and aminocatalysts, diastereodivergence can be achieved and any of the four diastereoisomers can be accessed in high diastereo- and enantio- selectivity.

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

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