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通过配体控制的选择性去芳构化 C2-芳基化和直接 C3-芳基化合成 2,2,5-三取代 2-吡咯和 2,3,5-三取代 1-吡咯。

Synthesis of 2,2,5-Trisubstituted 2-Pyrroles and 2,3,5-Trisubstituted 1-Pyrroles by Ligand-Controlled Site-Selective Dearomative C2-Arylation and Direct C3-Arylation.

机构信息

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.

出版信息

Org Lett. 2019 Sep 6;21(17):6972-6977. doi: 10.1021/acs.orglett.9b02559. Epub 2019 Aug 9.

Abstract

Palladium-catalyzed site-selective dearomative C2-arylation of 2,5-diaryl-1-pyrroles with aryl chlorides was accomplished, and a series of 2,2,5-triaryl-2-pyrroles were synthesized. In addition, the site selectivity of the reaction was switched by simply changing the ligand, and the direct C3-arylated 2,3,5-triaryl-1-pyrroles were prepared. The obtained 2,2,5-triaryl-2-pyrroles could be further transformed into 2,2,5,5-tetraarylpyrrolidines.

摘要

钯催化的 2,5-二芳基-1-吡咯与芳基氯的位点选择性去芳构 C2-芳基化反应已经完成,一系列 2,2,5-三芳基-2-吡咯被合成。此外,通过简单改变配体即可切换反应的位点选择性,直接制备 C3-芳基化的 2,3,5-三芳基-1-吡咯。得到的 2,2,5-三芳基-2-吡咯可以进一步转化为 2,2,5,5-四芳基吡咯烷。

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