Synthesis of a C-7 Pd-glycosyl-donor via the base promoted alkylative CO2 trapping with 2-acetylfuran

Journal of CO2 Utilization(2021)

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摘要
A practical one pot alkylative carboxylation of 2-acetylfuran was developed. The reaction was optimized for the synthesis of methyl β-ketoesters. The β-keto-ester product was used in the asymmetric synthesis of a C-7 pyranone precursor for a Pd-glycosylation reaction, with the goal of its use in the synthesis of pyran containing natural products, such as Aspergillide C.
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关键词
Alkylative carboxylation,Asymmetric synthesis,Noyori reduction,Achmatowicz rearrangements,2-Acetylfuran synthesis
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