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Stereodivergent Synthesis of Alkaloid (±)-223A and (±)-6-epi-223A via Rh-Catalyzed Hydroformylation Double Cyclization.
Huang, Wen-Wei; Cheng, Jui-Teng; Hsiao, Wei-Ting; Chiou, Wen-Hua.
Afiliação
  • Huang WW; Department of Chemistry, National Chung-Hsing University, Taichung 402202, Taiwan, R.O.C.
  • Cheng JT; Department of Chemistry, National Chung-Hsing University, Taichung 402202, Taiwan, R.O.C.
  • Hsiao WT; Department of Chemistry, National Chung-Hsing University, Taichung 402202, Taiwan, R.O.C.
  • Chiou WH; Department of Chemistry, National Chung-Hsing University, Taichung 402202, Taiwan, R.O.C.
J Org Chem ; 89(7): 5091-5097, 2024 Apr 05.
Article em En | MEDLINE | ID: mdl-38456271
ABSTRACT
A stereodivergent approach toward total syntheses of Dendrobatid alkaloids 223A and 6-epi-223A is described. The approach features a concise construction of an indolizidine skeleton by Rh-catalyzed domino hydroformylation double cyclization and sequential stereocontrolled transformations such as reductive alkylation or anti-selective α-alkylation of the 5-oxoindolizidine. These stereoselective reactions afford the desired stereochemistry in the targets.

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