𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Dipolar addition reactions of nitrile oxides. VII. A new general method of synthesis of 3,5-disubstituted 1,2,4-oxadiazoles.

✍ Scribed by P. Rajagopalan


Publisher
Elsevier Science
Year
1969
Tongue
French
Weight
127 KB
Volume
10
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


We would like to report that aliphatic and aromatic nitrile oxides (I), as exemplified by pivalonitrile oxide and I-chlorobenzonitrile oxide respectively, react with methyl imidates (II) at room temperature (in absolute ether) to yield 1.2,4-oxadiazoles of the type III (See Table ).


πŸ“œ SIMILAR VOLUMES


A new synthesis of symmetrical 2,5-disub
✍ Fouad Bentiss; Michel LagrenΓ©e πŸ“‚ Article πŸ“… 1999 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 182 KB πŸ‘ 1 views

## Abstract Several new 2,5‐disubstituted 1,3,4‐oxadiazoles have been synthesized in good yields by reaction of aromatic acids with hydrazine dihydrochloride in a mixture of orthophosphoric acid, phosphorus pentoxide and, in general, with addition of phosphorus oxychloride to the reaction mixture.

New one step synthesis of 3,5-disubstitu
✍ Moha Outirite; Mounim Lebrini; Michel LagrenΓ©e; Fouad Bentiss πŸ“‚ Article πŸ“… 2007 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 199 KB πŸ‘ 1 views

## Abstract magnified image Disubstituted 1,2,4‐oxadiazoles have been synthesized in good yields and good purity in one pot procedure by reaction of aromatic nitriles, hydroxylamine hydrochloride and sodium carbonate in ethylene glycol under heating at 195Β°C. The structures of different 1,2,4‐oxad