Abstract
The oxidative decyanation of secondary nitriles to ketones was effected by trapping nitrile anions with molecular oxygen, reducing the resulting α-hydroperoxynitriles to cyanohydrins with stannous chloride, and converting the cyanohydrins to ketones with sodium hydroxide.
| Original language | English |
|---|---|
| Pages (from-to) | 267-268 |
| Number of pages | 2 |
| Journal | Journal of Organic Chemistry |
| Volume | 40 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 1 1975 |
ASJC Scopus subject areas
- Organic Chemistry
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