## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Formation of Diazo Compounds on Decomposition of 2,3-Diazabicyclo[3.1.0]hex-2-enes:[3+2]-Cycloreversions
β Scribed by Dr. Manfred Schneider; Bernd Csacsko
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 316 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0044-8249
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β¦ Synopsis
Table 1. Selected physical properties of ( 5 a ) and (56) "C-NMR (in CDCl3, T M S internal) c-1 109.2 C-CN 97.4, 98.9, 102.0 c-4 108.9 c -5 c-1 ' 124.5 c -2 , c-3' 131.1 IR ( K B r ) [cm-'1 C=N 2210 Cyclopropene [5] 1898, 1550 UV(CH3CN) [ n m l (log&) 240 (4.61), 278 (4.23) 'H-NMR (100 MHz, CDClj, T M S internal) 4-H 6.78 (1 H, s) 5-H 109.9 97.7, 101.7, 102.5 105.1 124.8
π SIMILAR VOLUMES
Polymerization behavior of meta-naphthoquinone methide, 3,4-benzo-6methylenebicyclo[3.1.0]hex-3-ene-2-one ( 1), was studied. Radical initiator 2,2-azobis(isobutyronitrile) (AIBN) induced polymerization of 1, but ionic initiators potassium tert-butoxide, butyllithium, and boron trifluoride etherate d
on the occasion of his 75th birthday