A selective protocol for the synthesis of azole ureas and diheterocycle substituted methanimines from nitrogenous heterocycles and isocyanides was established under electrochemical reaction conditions. By adjustment of the reaction conditions such as electrode materials and solvents, two different types of heterocyclic derivatives of significant value could be selectively obtained with high yields. The reactions have several advantages such as simple reaction conditions and high chemoselectivity and are suitable for various nitrogenous heterocycles and isocyanides.
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Tan Zhang
Wei Wang
MingQi Chen
Organic Letters
Collaborative Innovation Center of Chemistry for Energy Materials
Nanjing Normal University
Institute of Molecular Functional Materials
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Zhang et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69a3d8b8ec16d51705d2fdff — DOI: https://doi.org/10.1021/acs.orglett.6c00189
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