Cascade and one-pot processes providing substituted quinolines from aldimines and allylsilanes: auto-tandem catalysis of triflic imide

Cascade and one-pot processes providing substituted quinolines from aldimines and allylsilanes: auto-tandem catalysis of triflic imide
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DOI:
10.1016/j.tetlet.2007.05.032
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发表时间:
2007-07-02
影响因子:
1.8
通讯作者:
Takasu, Kiyosel
Takasu, Kiyosel
中科院分区:
化学4区
文献类型:
--
作者:
Shindoh, Naoya;Tokuyama, Hidetoshi;Takasu, Kiyosel

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我们已经证明了级联反应和一锅反应,它们构成了反电子需求的杂Diels-Alder反应和氧化芳构化,以提供取代的喹啉来生成芳香醛二胺和烯丙基硅烷。级联过程包括自动串联催化;Tf2NH激活这些机械上不同的反应。我们发现,从苯胺、醛和烯丙基硅烷开始的多组分工艺也是可行的。(C)2007爱思唯尔有限公司。保留所有权利。
We have demonstrated cascade and one-pot reactions, which constitute inverse electron demand hetero-Diels-Alder reaction and oxidative aromatization, to provide substituted quinolines to form aryl aldimines and allylsilanes. The cascade process involves an auto-tandem catalysis; Tf2NH activates these mechanistically distinct reactions. We have found that a multicomponent process starting from aniline, aldehyde, and allylsilane is also available. (c) 2007 Elsevier Ltd. All rights reserved.