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 |
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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