Controlling the Symmetry of Perylene Derivatives via Selective ortho-Borylation.

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-03-07 Epub Date: 2025-02-27 DOI:10.1021/acs.joc.4c02669
David Sánchez-Fernández, Tomás Torres, José García-Calvo
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Abstract

This work presents a systematic and rational approach to the synthesis of previously reported as well as novel tetra- and di-ortho-borylated perylene, perylenediimide, and perylenemonoimide scaffolds. Through optimization of the reaction conditions, employing [Ir(OMe)(COD)]2 as a catalyst and suitable ligands, efficient tetraborylation and regioselective diborylations were achieved. Additionally, the reaction times were reduced from days to hours under microwave irradiation, rendering this methodology a practical and scalable route for the ortho-functionalization of perylene derivatives.

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选择性邻位硼化反应控制苝衍生物的对称性。
这项工作提出了一个系统和合理的方法来合成以前报道的以及新的四和二邻硼化苝,苝二酰亚胺和苝酰氨基亚胺支架。通过优化反应条件,以[Ir(OMe)(COD)]2为催化剂和合适的配体,实现了高效的四硼化和区域选择性二硼化反应。此外,在微波照射下,反应时间从几天缩短到几小时,使该方法成为苝衍生物邻位官能化的实用和可扩展的途径。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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