Facile 5-Endo Amidyl Radical Cyclization Promoted by Vinylic Iodine Substitution
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https://figshare.com/articles/dataset/Facile_5_Endo_Amidyl_Radical_Cyclization_Promoted_by_Vinylic_Iodine_Substitution/3374890
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资源简介:
BF3·OEt2-catalyzed atom-transfer radical addition of iodoacetamides to alkynes yielded the corresponding vinyl iodides, which upon treatment
with tBuOCl and I2 afforded γ-lactam derivatives in moderate to good yield. The mechanism was proposed to be 5-endo amidyl radical cyclization,
and vinylic iodine substitution provided the driving force for the cyclization.
创建时间:
2016-05-12



