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N-取代(4R,7S)-4-甲基-7-异丙基己内酰胺的合成研究

Synthesis of N-substituted(4R,7S)-7-isopropyl-4-methylazepan-2-one
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摘要 从薄荷酮出发经肟化反应,贝克曼重排反应,以及酰基化反应,合成了一系列标题化合物,其中N-乙酰基取代的产物的产率高达94.8%。通过1HNMR和13CNMR对各步产物进行了表征。 A series of N-substituted ( 4R, 7S ) -7-isopropyl-4- methy]azepan-2-one was synthesized from menthone via oxi- mation,beckmann rearrangement and acyiation. The yield of the acetylation was up to 94.8%. The structures of the products were confirmed by ^1HNMR and ^13 CNMR.
作者 任芳 阳年发
出处 《化学试剂》 CAS CSCD 北大核心 2011年第11期975-977,共3页 Chemical Reagents
基金 国家自然科学基金资助项目(20772102) 湖南省自然科学基金资助项目(08jj3013)
关键词 薄荷酮 薄荷酮肟 贝克曼重排 酰基化 (4R 7S)-4-甲基-7-异丙基己内酰胺 menthone menthone oxime Beckmann rearrangement acylation ( 4R, 7S ) -7 -isopropyl-4-methylazepan-2-one
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参考文献6

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