Metal-free synthesis of highly substituted 2-aminopyridines by formal [3+3] annulation of α,α-dicyanoalkenes with imines
Abstract
A metal-free formal [3+3] annulation of α,α-dicyanoalkenes with Ncyanoimines is reported. This strategy provides a straightforward and efficient route for the construction of highly substituted 2-aminopyridines with good yields and high chemoselectivity. The practical synthetic utility of this methodology is demonstrated by structural diversification of the products and further derivatization into bioactive molecules.
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