Thermal Rearrangement of Pyridylnitramines. -In contrast to their N-methyl analogues, which rearrange to form the corresponding methylamino-nitroamines in 74-90% yield, 2-substituted pyridine (I) rearranges into two regioisomers (II) and (III), 4-substituted pyridine (IV) is much less prone to rear
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ChemInform Abstract: Thermal Rearrangement of Aromatic Acetal and Thioacetal Derivatives.
β Scribed by A. M. GABER; M. M. ALY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 27 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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