ナトリウムアミドによるピコリルエーテルの転位反応(第2報)樟脳環の開裂(第5報)7-Hydroxy-π-apocamphane及び1-Hydroxy-10-apocamphor
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概要
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Allylpyridylcarbinols (α or γ) were obtained from allyl picolyl ethers (α or γ) by the application of sodium amide in benzene. When the same reactions was carried out in xylene at 130〜140° , the yield of rearrangement product increased in the γ-compound, while a non-viscous oil was obtained from the α-compound. This non-viscous oily product was found to be identical with propyl α-pyridyl ketone.
- 公益社団法人日本薬学会の論文
- 1956-12-20
著者
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