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铜和钯催化的分子内C-S键形成:2-氨基苯并噻唑的简便合成方法

Copper- and palladium-catalyzed intramolecular C-S bond formation: a convenient synthesis of 2-aminobenzothiazoles.

作者信息

Joyce Laurie L, Evindar Ghotas, Batey Robert A

机构信息

Davenport Research Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, Canada M5S 3H6.

出版信息

Chem Commun (Camb). 2004 Feb 21(4):446-7. doi: 10.1039/b311591g. Epub 2004 Jan 28.

Abstract

Copper- and palladium-catalyzed intramolecular C-S bond formation by cross-coupling between an aryl halide and thiourea functionality is demonstrated for the synthesis of 2-aminobenzothiazoles, wherein the Cu-catalyzed protocol is generally superior and more cost effective than the Pd-catalyzed protocol; the Cu-catalyzed reaction also further expands recent studies exploring the utility of Cu salts as replacements for Pd in carbon-heteroatom bond-forming reactions. A one-pot variant combining the synthesis of the thiourea and the cyclization was also demonstrated.

摘要

通过芳基卤化物与硫脲官能团之间的交叉偶联实现的铜和钯催化的分子内C-S键形成反应被用于2-氨基苯并噻唑的合成,其中铜催化的方法通常比钯催化的方法更优越且更具成本效益;铜催化的反应还进一步扩展了最近关于探索铜盐在碳-杂原子键形成反应中替代钯的实用性的研究。还展示了一种将硫脲合成与环化相结合的一锅法变体。

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