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Catalytic Epoxidation of Carbonyl Compounds via Carbonyl Ylides: from Racemic to Enantioselective.
Qi, Lin-Jun; Zhou, Bo; Ye, Long-Wu.
Afiliação
  • Qi LJ; School of Pharmaceutical and Chemical Engineering &, Institute for Advanced Studies, Taizhou University, Taizhou, Zhejiang, 318000, P. R. China.
  • Zhou B; Key Laboratory for Chemical Biology of Fujian Province and State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, Xiamen University, Xiamen, 361005, P. R. China.
  • Ye LW; Key Laboratory for Chemical Biology of Fujian Province and State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, Xiamen University, Xiamen, 361005, P. R. China.
Chemistry ; 30(41): e202401389, 2024 Jul 19.
Article em En | MEDLINE | ID: mdl-38779789
ABSTRACT
Transition metal-catalyzed epoxidation of carbonyl compounds through carbonyl ylides represents a highly effective method for synthesizing a diverse range of valuable epoxides. This review offers an in-depth overview of the latest developments in inter- and intramolecular epoxidation reactions involving metal carbenes and carbonyl compounds, encompassing both racemic to enantioselective transformations. These catalytic epoxidations are reviewed by highlighting their product selectivity, diversity and applicability, and the related mechanistic rationale is showcased where possible.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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