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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >2-allyl-N-benzyl substituted alpha-naphthylamines as building blocks in heterocyclic synthesis. New and efficient syntheses of benz[e]naphtho[1,2-b]azepine and naphtho[1,2-b]azepine derivatives
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2-allyl-N-benzyl substituted alpha-naphthylamines as building blocks in heterocyclic synthesis. New and efficient syntheses of benz[e]naphtho[1,2-b]azepine and naphtho[1,2-b]azepine derivatives

机译:2-烯丙基-N-苄基取代的α-萘胺作为杂环合成的基础。苯并[e]萘并[1,2-b]氮杂和萘并[1,2-b]氮杂的新型高效合成方法

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摘要

A new series of 13-acetyl-7,12-dihydro-7-ethylbenz[e]naphtho[1,2-b]azepine (4a-d) and 2-aryl-4-hydroxy-2,3,4,5-tetrahydronaphtho[1,2-b]azepine derivatives (6a-d) have been synthesized from N-allyl-N-benzyl substituted alpha-naphthylamines (1a-d) by utilizing aromatic amino-Claisen rearrangement, intramolecular Friedel-Crafts alkylation and intramolecular dipolar 1,3-cyclo-addition nitrone-olefin reactions. (c) 2006 Elsevier Ltd. All rights reserved.
机译:一系列新的13-乙酰基-7,12-二氢-7-乙基苯并[e]萘[1,2-b]氮杂(4a-d)和2-芳基-4-羟基-2,3,4,5通过利用芳族氨基克莱森重排,分子内弗瑞德-克来福特烷基化和分子内偶极1,3-环加成的硝烯-烯烃反应。 (c)2006 Elsevier Ltd.保留所有权利。

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