Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218012 | Tetrahedron | 2013 | 14 Pages |
Abstract
In the course of our studies on Cerpegin analogues synthesis, a serendipitous reactivity of enaminolactone nitrile has been observed. Instead of expecting iminocerpegins, we have gained new class of substituted 2-aminopyridines. The methodology has been applied on a wide range of primary amines, as aliphatic, aromatic, heteroaromatic and also, diamines, hydrazines and chiral amines.
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