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钯催化的1-炔基-2-碘-D-葡糖醛的羰基化环化反应

Palladium-Catalyzed Carbonylative Cyclization of 1-Alkynyl-2-iodo-d-glucal.

作者信息

Hornink Milene M, Figlino Giuseppe E, Toledo Mônica F Z J, Pimenta Daniel C, Stefani Hélio A

机构信息

Faculdade de Ciências Farmacêuticas, Departamento de Farmácia, Universidade de São Paulo, São Paulo, SP 05508-220, Brazil.

Centro Universitário São Camilo, São Paulo, SP 05585-000, Brazil.

出版信息

Org Lett. 2024 Oct 11;26(40):8621-8625. doi: 10.1021/acs.orglett.4c03337. Epub 2024 Sep 30.

Abstract

Cascade reactions are important synthetic tools for the synthesis of heterocyclic molecules, particularly those catalyzed by palladium. Herein, we report a palladium-catalyzed aminocarbonylative cyclization of new 1-alkynyl-2-iodo-d-glucals, which undergo a tandem carbonylative cyclization in the presence of various amine nucleophiles. A broad range of aromatic and aliphatic amines were applied as coupling partners, resulting in the selective and high-yield synthesis of glycosides fused to pyridinones. A plausible mechanism is proposed, proceeding via a tandem palladium aminocarbonylation followed by a palladium-catalyzed cyclization.

摘要

级联反应是合成杂环分子的重要合成工具,尤其是那些由钯催化的反应。在此,我们报道了一种新型1-炔基-2-碘-d-葡糖醛的钯催化氨羰基化环化反应,该反应在各种胺亲核试剂存在下进行串联羰基化环化。多种芳香族和脂肪族胺被用作偶联伙伴,从而选择性地高产率合成了与吡啶酮稠合的糖苷。提出了一种合理的机理,该机理通过串联钯氨羰基化反应,然后是钯催化的环化反应进行。

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