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首页> 外文期刊>Chemistry of Natural Compounds >Heterocyclization of 3-aminocamphor and 3-aminoisoborneol derivatives with cyclic βdiketones and formaldehyde. synthesis of optically active 1, 2, 3, 4-tetrahydroquinoline derivatives with terpene substituents
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Heterocyclization of 3-aminocamphor and 3-aminoisoborneol derivatives with cyclic βdiketones and formaldehyde. synthesis of optically active 1, 2, 3, 4-tetrahydroquinoline derivatives with terpene substituents

机译:3-氨基樟脑和3-氨基异冰片醇衍生物与环状β二酮和甲醛的杂环化。具有萜烯取代基的光学活性1、2、3、4-四氢喹啉衍生物的合成

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摘要

Spirocyclic 1, 2, 3, 4-tetrahydroquinoline derivatives were prepared in quantitative yield by three-component condensation of dimedone or Meldrum's acid with formaldehyde and (1S, 3R, 4S)-1, 7, 7-trimethyl-3- (arylamino)bicyclo[2.2. 1]heptan-2-one or (1S, 2S, 3R, 4S)-1, 7, 7-trimethyl-3-(arylamino)bicyclo[2.2.1] heptan- 2-ol.
机译:螺环1,2,3,4-四氢喹啉衍生物是通过二甲酮或Meldrum's酸与甲醛和(1S,3R,4S)-1,7,7-三甲基-3-(芳基氨基)的三组分缩合反应以定量产率制备的双环[2.2。 1]庚烷-2-酮或(1S,2S,3R,4S)-1,7,7-三甲基-3-(芳基氨基)双环[2.2.1]庚烷-2-醇。

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