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CuCl-Induced Formation and Migration of Isoindazolyl Carbenoids

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/CuCl_Induced_Formation_and_Migration_of_Isoindazolyl_Carbenoids/3015874
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Two azo-ene-butadiyne conjugated systems undergo CuCl-mediated cyclization to afford isoindazolyl carbenoids that could be trapped with 2,3-dimethyl-2-butene as [2 + 1] cycloaddition products. X-ray structure analysis of the resultant cyclopropanes showed that formal migration to the distal carbenoid isomer and subsequent trapping had occurred. The possible CuCl-induced cyclization/migration pathways were explored using density functional theory, which indicated that the reaction most likely occurred via coordination of CuCl to the distal alkyne bond.
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2007-03-30
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