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首页> 外文期刊>The Journal of Organic Chemistry >One-Pot Synthesis of Substituted Benzo[b]furans and Indoles from Dichlorophenols/Dichloroanilines Using a Palladium - Dihydroxyterphenylphosphine Catalyst
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One-Pot Synthesis of Substituted Benzo[b]furans and Indoles from Dichlorophenols/Dichloroanilines Using a Palladium - Dihydroxyterphenylphosphine Catalyst

机译:钯-二羟基叔苯基膦催化一锅法合成二氯苯酚/二氯苯胺一并取代苯并[b]呋喃和吲哚

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摘要

Disubstituted benzo[b]furans were synthesized by ortho-selective Sonogashira coupling of dichlorophenols and terminal alkynes, followed by cyclization and Suzuki-Miyaura coupling in one pot, using a palladium-dihydroxyterphenylphosphine (Cy-DHTP) catalyst. The use of substoichiometric amounts of tetrabutylammonium chloride was effective in accelerating the Suzuki-Miyaura coupling. This protocol was also successfully applied to the one-pot synthesis of disubstituted indoles from dichloroaniline derivatives.
机译:二取代的苯并[b]呋喃是通过二氯苯酚和末端炔烃的邻位选择性Sonogashira偶联反应,然后使用钯-二羟基叔苯基膦(Cy-DHTP)催化剂在一个罐中进行环化和Suzuki-Miyaura偶联而合成的。亚化学计量的氯化四丁基铵的使用可有效加速Suzuki-Miyaura偶联。该方案还成功地用于从二氯苯胺衍生物的一锅法合成二取代的吲哚。

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