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在聚苯乙烯树脂上合成多样吲哚文库 - 固载有机金属反应的范围和限制。

Synthesis of diverse indole libraries on polystyrene resin - Scope and limitations of an organometallic reaction on solid supports.

机构信息

Institute of Organic Chemistry, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, D-76131 Karlsruhe, Germany.

出版信息

Beilstein J Org Chem. 2012;8:1191-9. doi: 10.3762/bjoc.8.132. Epub 2012 Jul 26.

Abstract

The synthesis of diverse substituted indole structures on solid supports is described. The immobilization of nitrobenzoic acid onto Merrifield resin and the subsequent treatment with alkenyl Grignard reagents delivered indole carboxylates bound to solid supports. In contrast to results in the liquid phase, ortho,ortho-unsubstituted nitroarenes also delivered indole moieties in good yields. Subsequent palladium-catalyzed reactions (Suzuki, Heck, Sonogashira, Stille) delivered, after cleavage, the desired molecules in moderate to good yields over four steps. The scope and limitations are presented.

摘要

介绍了在固体载体上合成各种取代吲哚结构的方法。将硝基苯甲酸固载到 Merrifield 树脂上,然后用烯基格氏试剂处理,得到了连接在固体载体上的吲哚羧酸酯。与液相中的结果相反,邻、邻-未取代的硝基芳烃也以良好的收率得到了吲哚部分。随后的钯催化反应(Suzuki、Heck、Sonogashira、Stille)在裂解后,经过四步反应以中等至良好的收率得到了所需的分子。展示了该方法的适用范围和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc5a/3458737/c5f0fb68cf23/Beilstein_J_Org_Chem-08-1191-g006.jpg

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