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使用钯催化反应的吲哚羧酸盐的固相合成

Solid-phase synthesis of indolecarboxylates using palladium-catalyzed reactions.

作者信息

Yamazaki Kazuo, Nakamura Yosuke, Kondo Yoshinori

机构信息

Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Aoba-ku, Sendai 980-8578, Japan.

出版信息

J Org Chem. 2003 Jul 25;68(15):6011-9. doi: 10.1021/jo0340307.

Abstract

Polymer-supported, palladium-catalyzed cyclization reactions effectively synthesized indolecarboxylates. Palladium-catalyzed carbon-carbon bond-forming reactions of immobilized enaminoesters followed by transesterification yielded indole 2- or 3-carboxylates with various functional groups on the benzene ring. Indolecarboxylates were efficiently cyclized via an intramolecular palladium-catalyzed amination reaction of immobilized N-substituted dehydrohalophenylalanines, and immobilized N-acetyl-dehydroalanines were efficiently converted into indolecarboxylates via tandem Heck-amination reactions.

摘要

聚合物负载的钯催化环化反应有效地合成了吲哚羧酸酯。固定化烯胺酯的钯催化碳-碳键形成反应,随后进行酯交换反应,得到了苯环上带有各种官能团的吲哚-2-羧酸酯或吲哚-3-羧酸酯。吲哚羧酸酯通过固定化的N-取代脱氢卤代苯丙氨酸的分子内钯催化胺化反应有效地环化,并且固定化的N-乙酰基脱氢丙氨酸通过串联Heck-胺化反应有效地转化为吲哚羧酸酯。

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