Tabelle I. ' H-NMR-Daten des Nickelacyclobutabenzolteils der Verbindungen 5 (400 MHz [a], [D,]THF, -8 O T [b]. 6-Werte bezogen auf TMS).
Rearrangement of 4H-1,2,4-Triazolium Salts to 4-Acyl-5-aminoimidazoles
β Scribed by Dr. Costin N. Rentzea
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 231 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The fragmentation behaviour of 3,4-disubstituted 1,2,4-oxadiazole-5(4H)-thiones under electron impact (EI) can be explained by postulating a predominant rearrangement to the corresponding 3,4-disubstituted 1,2,4-thiadiazole-5(4H)-ones before further fragmentation. This postulate is confirmed by a co
highly-aggregated dilithiated organics akin to 1 include the nitrile dodecamer 2[6a1 and the sulfone hexamer 3.[6bl It is also noteworthy that the core of 1 can be considered as belonging to the fluorite (CaF,) structural type (N corresponding to Ca, Li to F ) and that even the "external" Et,O-compl