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Chemoselective Synthesis of Polycyclic Spiroindolines and Polysubstituted Pyrroles via the Domino Reaction of 2‑Isocyanoethylindoles

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Chemoselective_Synthesis_of_Polycyclic_Spiroindolines_and_Polysubstituted_Pyrroles_via_the_Domino_Reaction_of_2_Isocyanoethylindoles/2253373
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资源简介:
Chemoselective 2-isocyanoethylindole-based domino reactions for the construction of polycyclic spiroindoline derivatives and polysubstituted pyrroles have been developed. The reaction of 2-isocyanoethylindoles and gem-diactivated olefins lead to the polycyclic spiroindoline derivatives (up to 92% yields) in EtOH under reflux conditions. Furthermore, the three-component reaction of 2-isocyanoethylindoles with gem-diactivated olefins and secondary amines afford polysubstituted pyrroles (in moderate yields) in CH3CN under reflux conditions.
创建时间:
2016-02-16
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