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Synthesis of carbazoles and dibenzofurans via cross-coupling of o-iodoanilines and o-iodophenols with silylaryl triflates and subsequent Pd-catalyzed cyclization

机译:通过邻碘苯胺和邻碘苯酚与甲硅烷基芳基三氟甲磺酸酯的交叉偶联以及随后的Pd催化环化反应合成咔唑和二苯并呋喃

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摘要

An efficient route to a variety of carbazoles and dibenzofurans has been developed. It involves the reaction of o-iodoanilines or o-iodophenols with silylaryl triflates in the presence of CsF to afford the N- or O-arylated products, which are subsequently cyclized using a Pd catalyst to carbazoles and dibenzofurans in good to excellent yields. By using this methodology, the carbazole alkaloid, mukonine has been synthesized in 76% overall yield in three steps. (c) 2006 Elsevier Ltd. All rights reserved.
机译:已经开发出一种有效的途径来生产各种咔唑和二苯并呋喃。它涉及在CsF存在下,邻碘苯胺或邻碘苯酚与甲硅烷基芳基三氟甲磺酸酯反应,生成N-或O-芳基化产物,随后使用Pd催化剂将其环化成咔唑和二苯并呋喃,收率高至优异。通过使用这种方法,咔唑生物碱,鼠李碱已通过三个步骤以76%的总收率合成。 (c)2006 Elsevier Ltd.保留所有权利。

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