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铱(III)催化的硫醚导向芳烃C-H烯基化反应。

Ir(iii)-catalyzed thioether directed arene C-H alkenylation.

作者信息

Li Chen, Chen Xian, Bao Rui-Peng, Li Dong-Li, Zhang Kun, Wang Dong-Hui

机构信息

School of Biotechnology & Health Sciences, Wuyi University 22 Dongcheng Vill. Jiangmen Guangdong 529020 China

CAS Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Center for Excellence in Molecular Synthesis, University of Chinese Academy of Sciences, Shanghai Institute of Organic Chemistry, CAS 345 Lingling Rd. Shanghai 200032

出版信息

RSC Adv. 2019 Sep 24;9(52):30134-30138. doi: 10.1039/c9ra06811b. eCollection 2019 Sep 23.

DOI:10.1039/c9ra06811b
PMID:35530243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9072104/
Abstract

In this study, we demonstrate an Ir(iii)-catalyzed thioether directed alkenylation of arene C-H bonds under mild reaction conditions. The selectivity for mono- or di-alkenylation is controlled by the concentration of alkene and oxidant loading. Various functional groups are tolerated, and moderate to good yields of alkenylated products are achieved.

摘要

在本研究中,我们展示了在温和反应条件下铱(III)催化硫醚导向的芳烃C-H键烯基化反应。单烯基化或二烯基化的选择性由烯烃浓度和氧化剂负载量控制。该反应能耐受各种官能团,并获得了中等至良好产率的烯基化产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b04/9072104/bda59d09043a/c9ra06811b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b04/9072104/da59bc5ae4cd/c9ra06811b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b04/9072104/bda59d09043a/c9ra06811b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b04/9072104/da59bc5ae4cd/c9ra06811b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b04/9072104/bda59d09043a/c9ra06811b-f2.jpg

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本文引用的文献

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Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis.用于钯(II)催化的多功能杂芳基硫醚导向基团的合成与机理研究
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An overview of organosulfur compounds from Allium spp.: From processing and preservation to evaluation of their bioavailability, antimicrobial, and anti-inflammatory properties.大蒜属植物中的有机硫化合物概述:从加工和保存到评估其生物利用度、抗菌和抗炎特性。
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