Abstract
Preparation of 2,3‐Dimethyl‐5,6‐dihydro‐4H‐1,2‐oxaziniumiodide was achieved by N‐alkylation of 3‐methyl‐5,6‐dihydro‐4H‐1,2‐oxazine. Reactions with C‐nucleophiles led to the corresponding N‐methyl‐perhydro‐1,2‐oxazine derivatives. Reaction with sodium hydride in triglyme led to 3‐methyl‐4‐aza‐1,3‐pentadiene.
| Original language | English |
|---|---|
| Pages (from-to) | 2765-2767 |
| Number of pages | 3 |
| Journal | Helvetica Chimica Acta |
| Volume | 59 |
| Issue number | 8 |
| DOIs | |
| State | Published - 15 Dec 1976 |
| Externally published | Yes |
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