An unusual one step synthesis of acetylenes
β Scribed by Pradeep G. Karmarkar; Alka A. Thakar; Murzban S. Wadia
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 118 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Substituted nitrostyrenes on reaction with H202/NEt3 give 1,2 diary1 acetylenes in w 30 $ yield. Nitro olefins have been converted' to epoxy nitro compounds by rsaction with H202/-OH. However it has been reported' that this reaction Fails in the case of g -nitrostyrene es the epoxide derived From it contains an acidic hydrogen. In order to circumvent this problem we attempted epoxidation with H202/NEt3. Under these conditions we observed ^_ ..I..^.._, ^_^ ^L_^ _..-LL__:_ _P _..__^._I^_, _--L..l---c) _*__l.1__ ..**I_ QI, "IIv3ual "I,tl JLmp ayll~rlesrs: "I symmarr*u;ar auarylena 6, starring w&&n compound A.
π SIMILAR VOLUMES
**Eine ergiebige, einstufige Synthese von 2βImidazolinβ4(5)βon** Die Titelverbindung **4**, das lange bekannte biologische Zwischenprodukt beim Abbau von Xanthin zu __N__β(Iminomethyl)glycin, wird in einer einstufigen Umsetzung von Aminoacetonitrilhydrochlorid mit ΓΌberschΓΌssigem Trimethylβorthoform
## Abstract For Abstract see ChemInform Abstract in Full Text.
Five naturally occurring bases with an oxasole ring have been known to date, all bearing substituent at 2 and 5 position l-4) and because of their relatively
The use of 8-polycarbonyl compounds in biogenetic-type syntheses' was developed especially by Collie', Robinson', and Birch'. Robinson6 suggested