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通过钯催化的羰基化反应构建稠合多杂环结构的位点选择性双环化和四环化路线

Site-Selective Double and Tetracyclization Routes to Fused Polyheterocyclic Structures by Pd-Catalyzed Carbonylation Reactions.

作者信息

Pancrazzi Francesco, Sarti Nicolò, Mazzeo Paolo P, Bacchi Alessia, Carfagna Carla, Mancuso Raffaella, Gabriele Bartolo, Costa Mirco, Stirling András, Della Ca' Nicola

机构信息

Department of Chemistry, Life Sciences and Environmental Sustainability (SCVSA) , University of Parma , Parco Area delleScienze, 17/A , 43124 Parma , Italy.

CIRCC , Via Celso Ulpiani, 27 , 70126 Bari , Italy.

出版信息

Org Lett. 2020 Feb 21;22(4):1569-1574. doi: 10.1021/acs.orglett.0c00171. Epub 2020 Feb 3.

Abstract

In this contribution, we report novel palladium-catalyzed carbonylative cascade approaches to highly functionalized polyheterocyclic structures. The Pd-catalyzed carbonylative process involves the regioselective insertion of one to three CO molecules and the sequential ordered formation of up to eight new bonds (one C-O, two C-C, five C-N). The exclusive formation of six-membered heterocycles is elucidated by detailed modeling studies.

摘要

在本论文中,我们报道了新颖的钯催化羰基化级联反应方法,用于构建高度官能化的多杂环结构。钯催化的羰基化过程涉及一至三个CO分子的区域选择性插入以及多达八个新键(一个C-O键、两个C-C键、五个C-N键)的顺序有序形成。详细的模型研究阐明了六元杂环的专一性形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52e7/7307965/1d526e25d2ca/ol0c00171_0001.jpg

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