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v-triazolines. Part XIV . 1-aryl-5-dialkylaminomethyl-4-methylene-4,5-dihydro-v-triazoles

✍ Scribed by Donato Pocar; Luisa Maria Rossi; Pasqualina Trimarco


Book ID
112125936
Publisher
Journal of Heterocyclic Chemistry
Year
1980
Tongue
English
Weight
235 KB
Volume
17
Category
Article
ISSN
0022-152X

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πŸ“œ SIMILAR VOLUMES


v-Triazolines, XXIV. Pyrazolecarbaldehyd
✍ Destro, Riccardo ;Erba, Emanuela ;Forti, Luciana ;Pocar, Donato ;Scarcella, Dani πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 English βš– 624 KB

## Abstract The sydnones **1a**–**c** react with the 4,5‐dihydro‐__v__‐triazoles **2a**–**c** by long refluxing at 110– 140Β°C affording __via__ non‐isolable adducts with elimination of CO~2~ and N~2~ and rearrangement a mixture of 4,5‐dihydropyrazoles **3a**– **c**, 3‐pyrazolecarbaldehyde anils **4

Dihydro azoles and free radicals : Part
✍ Nicoletta Almirante; Stefano Cicardi; Caterina Napoletano; Marco Serravalle πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 French βš– 409 KB

I-Aryl-4-methylene-5-morpholino-v-triazolines 1 were reacted with halomethyl radicals generated by reaction of=halo methanes 2 with benzoyl peroxide or copper(I)chlori In theformer case the corresponding I-aryl-4-trihaloethyl-v-triazoles 1 and I-aryl-4-halomethyl-v-triazoles 4 were formed. In the