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Metal-Free Synthesis of Functionalized Indolizines via a Cascade Michael/SN2/Aromatization Reaction of 2‑Alkylazaarene Derivatives with Bromonitroolefins

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Figshare2024-12-09 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Metal-Free_Synthesis_of_Functionalized_Indolizines_via_a_Cascade_Michael_S_sub_N_sub_2_Aromatization_Reaction_of_2_Alkylazaarene_Derivatives_with_Bromonitroolefins/27990452
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A transition metal-free domino Michael/SN2/aromatization annulation of 2-pyridylacetates with bromonitroolefins has been developed. A wide range of substrates containing various substituted groups was compatible with the present methodology and afforded functionalized indolizines with moderate to excellent yield (up to 99% yield). In addition, the potential practicality of the method stood out through scale-up reactions and further transformations to other valuable compounds. In our view, this study is an essential complement for the rapid construction of indolizine derivatives through a metal-free strategy.
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2024-12-09
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