Aziridinylketones and their cyclic anils. 12
β Scribed by V. D. Orlov; Z. Kaluski; N. P. Borob'eva; E. Figas; A. A. Tishchenko; F. G. Yaremko
- Publisher
- Springer US
- Year
- 1994
- Tongue
- English
- Weight
- 580 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0009-3122
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π SIMILAR VOLUMES
AZIRIDINYL KETONES AND THEIR CYCLIC ANILS. 9.\* SUBSTITUTED 1,3-DIAZABICYCLO[3.1.0]HEX-3-ENES Z. Kaluski, A. Gresyak-Figas, N, P. Vorob'eva, A. I. Bakumenko, F. G. Yaremenko, and V. D. Orlov UDC were obtained by the reaction of a,8-dibromodihydrochalcones with ammonia and formaldehyde (or acetone).
The reaction of 4-R-substituted (R = Br, CI, OC2H s, CmN, NO 2) 1,2-phenylenediamines with 1,3-diaryl-2,3-dibromo-l-propanones in the presence of triethylamine gave 1,2-diaryl-5-R-l,la-dihydroazirino[l,2-a]quinoxalines, which undergo isomerization in an acidic medium to give 2-aryl-3-arylmethylene-7
## Abstract **Summary:** The radical polymerization of different substituted methyl 2β(bicyclo[3.1.0]hexβ1βyl) acrylates, **1a**β**f**, was initiated by 2,2β²βazoisobutyronitrile (AIBN) at 65βΒ°C in chlorobenzene. The radical homopolymerization of **1a**β**f** occurred through the opening of the cycl