A New Ring Contraction Rearrangement of 2,5-and 3,6-Di-tertbutyl-3H-azepines to Pyridine Derivatives. -A novel ring contraction reaction of di-tert-butyl-substituted 3H-azepines furnishing pyridine derivatives under bromination conditions is described. A plausible mechanism for the rearrangement via
β¦ LIBER β¦
Difference in Photochemical Behavior in 3,6- and 2,5-Di-tert-butyl-3H-azepine: The First Photochemical Bond Formation Between 2- and 6-Position of 3H-Azepine Ring.
β Scribed by Kyosuke Satake; Shizuka Takami; Yuko Tawada; Masaru Kimura
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 118 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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