4.8 Article

Highly Efficient Cyanoimidation of Aldehydes

Journal

ORGANIC LETTERS
Volume 11, Issue 23, Pages 5482-5485

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol902207h

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Cyanoimidation of aldehydes using cyanamide as a nitrogen source and using NBS as an oxidant was achieved in high yields without the addition of a catalyst. The method has several advantages, Including mild conditions, simple workflow, and inexpensive reagents. The reaction proceeds in a one-pot manner, giving rise to the formation of intermolecular C-N and C-O bonds. Subsequently, the substituted N-cyanobenimidate products may also undergo a cyclization reaction to give 1,2,4-triazole derivatives in high yields.

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