An intramolecular [2 + 2] cycloaddition of ketenimines via palladium-catalyzed rearrangements of N-allyl-ynamides.
An intramolecular [2 + 2] cycloaddition of ketenimines via palladium-catalyzed rearrangements of N-allyl-ynamides.
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DOI:
10.1021/ol3013233
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发表时间:
2012-06-15
期刊:
影响因子:
5.2
通讯作者:
Walton, Mary C.
中科院分区:
文献类型:
--
作者:
DeKorver, Kyle A.;Hsung, Richard P.;Song, Wang-Ze;Wang, Xiao-Na;Walton, Mary C.
A cascade of Pd-catalyzed N-to-C allyl transfer–intramolecular ketenimine–[2 + 2] cycloadditions of N-allyl ynamides is described. This tandem sequence is highly stereoselective and the [2 + 2] cycloaddition could be rendered in a crossed or fused manner depending on alkene substitutions, leading to bridged and fused bicycloimines.
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