Dearomatization of aromatic asmic isocyanides to complex cyclohexadienes.

Dearomatization of aromatic asmic isocyanides to complex cyclohexadienes.
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DOI:
10.1038/s41467-022-33807-7
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发表时间:
2022-10-28
影响因子:
16.6
通讯作者:
Fleming, Fraser F.
Fleming, Fraser F.
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Altundas, Bilal;Alwedi, Embarek;Song, Zhihui;Gogoi, Achyut Ranjan;Dykstra, Ryan;Gutierrez, Osvaldo;Fleming, Fraser F.

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A dearomatization-dislocation-coupling cascade rapidly transforms aromatic isocyanides into highly functionalized cyclohexadienes. The facile cascade installs an exceptional degree of molecular complexity: three carbon-carbon bonds, two quaternary stereocenters, and three orthogonal functionalities, a cyclohexadiene, a nitrile, and an isocyanide. The tolerance of arylisocyanides makes the method among the mildest dearomatizations ever reported, typically occurring within minutes at −78 °C. Experimental and computational analyses implicate an electron transfer-initiated mechanism involving an unprecedented isocyanide rearrangement followed by radical-radical anion coupling. The dearomatization is fast, proceeds via a complex cascade mechanism supported by experimental and computational insight, and provides complex, synthetically valuable cyclohexadienes. As aromatic compounds can be obtained easily, their functionalization is a cornerstone of organic synthesis. Here, the authors report a dearomatization of aromatic isocyanides, installing three carbon-carbon bonds, two quaternary stereocenters, and three orthogonal functionalities in one operation.
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