v-Triazolines—VI: Rearrangement of triazolines from 2-substituted-1-aryl-and 1-heteroaryl-1-amino-ethylenes and tosylazide
✍ Scribed by Piero Dalla Croce; Riccardo Stradi
- Book ID
- 103401842
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 216 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract Pyrolysis of 4‐aryl‐5‐amino‐v‐triazolines affords, generally, amidines and/or benzanilides. Pyrolysis of 4‐aryl‐5‐morpholino‐v‐triazolines 6, together with the expected amidines 7 and/or aryanilides 8, produced the morpholinopyrroles 9. The reaction mechanism of this unusual transformat