Reaction of methanesulfonyl cyanide or p-toluenesulfonyl cyanide with carbon radicals generated from the acyl derivatives of N-hydroxy-2-thiopyridone gives the corresponding nitriles in high yield. A mechanistic scheme is suggested. There are many synthetic applications of carbon radicals generated
โฆ LIBER โฆ
Homologation of acids via carbon radicals generated from the acyl derivatives of N-hydroxy-2-thiopyridone. (The two-carbon problem).
โ Scribed by H.R. Derek; Chern Barton Ching-Yuh; Jaszberenyi Cs. Joseph
- Book ID
- 108382005
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 237 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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Oxygen centered radicals, formed by the photolysis of derivatives of N-hydroxy-2-thiopyridone, have been trapped by vinyl ethers. In the case of the benzoyloxy radical, smooth deoxygenation is effected by "'P compounds. Evidence for the formation of the dimethyltbutylsilyloxy and of the hydroxy rad