## Abstract Sodiumthiophenoxide and sodiumphenylselenide react with __N__‐benzyl‐ and __N__‐hexyl‐di‐__p__‐toluenesulfonamides (**1** and **2**) __via__ displacement at the C‐atom to afford the corresponding organosulfides and selenides in yields of 68–96%. In contrast, sodium cyanide converts disu
✦ LIBER ✦
Displacement of activated amino groups. The reaction of organocuprates with N,N-ditrifluromethanesulfonimides.
✍ Scribed by Paul Müller; Nguyen Thi Minh Phuong
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 197 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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