Journal of Organic Chemistry
Journal of Organic Chemistry
4 years ago

Pathways in the Degradation of Geminal Diazides

Pathways in the Degradation of Geminal Diazides
Andreas P. Häring, Thorsten Benter, Stefan F. Kirsch, Alexander Haack, Kristina Holzschneider, Daniel J. Corey
The degradation of geminal diazides is described. We show that diazido acetates are converted into tetrazoles through the treatment with bases. The reaction of dichloro ketones with azide anions provides acyl azides, through in situ formation of diazido ketones. We present experimental and theoretical evidence that both fragmentations may involve the generation of acyl cyanide intermediates. The controlled degradation of terminal alkynes into amides (by loss of one carbon) or ureas (by loss of two carbons) is also shown.

Publisher URL: http://dx.doi.org/10.1021/acs.joc.7b01019

DOI: 10.1021/acs.joc.7b01019

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