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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >The vilsmeier-Haack reaction on methyl homologues of N-benzyltetrahydrocarbazole (synthetic studies on indoles 52)
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The vilsmeier-Haack reaction on methyl homologues of N-benzyltetrahydrocarbazole (synthetic studies on indoles 52)

机译:N-苄基四氢咔唑的甲基同位物的vilsmeier-Haack反应(吲哚52的合成研究)

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摘要

To examine the steric effect in the Vilsmeier-Haack reaction of N-benzyl-1,2,3,4-tetrahydrocarbazole (1),the reactions were carried out on three methyl homologues of 1.It was found that 1-methyl- or 4,4,-dimethyl group has a large effect on reactivity due to their steric bulkiness.This result shows the importance of an initial attack at the 4a-position for the formation of these products.
机译:为了检查N-苄基-1,2,3,4-四氢咔唑(1)在Vilsmeier-Haack反应中的空间效应,对1个3个甲基同系物进行了反应,发现1-甲基或4,4,二甲基基团由于其空间体积大而对反应性有很大影响。此结果表明,在4a位上初始进攻对于形成这些产物的重要性。

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