正交Suzuki-Miyaura交叉偶联反应选择性合成[7]-[12]环对苯

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Evan R. Darzi, Thomas J. Sisto, Ramesh Jasti*
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引用次数: 138

摘要

利用两个后期中间体的顺序正交Suzuki-Miyaura交叉偶联反应,完成了[7]-[12]环对苯的发散性选择性合成。量子产率随着环对苯乙烯尺寸的减小而急剧下降,突出了较小的环对苯乙烯独特的光物理行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions

Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions

The divergent, selective syntheses of [7]–[12]cycloparaphenylenes have been accomplished utilizing sequential, orthogonal Suzuki–Miyaura cross-coupling reactions from two late-stage intermediates. Quantum yields decrease dramatically as cycloparaphenylene size decreases, highlighting the unique photophysical behavior of the smaller cycloparaphenylenes.

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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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