期刊
CHINESE JOURNAL OF CHEMISTRY
卷 39, 期 6, 页码 1611-1615出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cjoc.202000700
关键词
C— C activation; Palladium; C— C coupling; Ring‐ opening; Methylenecyclobutanes
资金
- National Natural Science Foundation of China [21703051, 22072035]
- Zhejiang Provincial Natural Science Foundation of China [LY18B020013, LZ186020001]
- Hangzhou Science and Technology Bureau of China [20180432605]
In this study, a novel palladium-catalyzed C-C bond activation of methylenecyclobutanes followed by Suzuki cross-coupling reaction was reported, leading to the formation of multisubstituted indanes. The tandem reaction process involves intramolecular carbopalladation of double bond, beta-carbon elimination, and intermolecular trapping of the transient sigma-alkylpalladium complex with boronic acids. A new TADDOL-derived phosphoramidite ligand containing fluorine and silicon-based bulky groups was found to be efficient for C-C bond activation of methylenecyclobutanes.
Main observation and conclusion Transition-metal catalyzed C-C bond activation is a formidable challenge owing to the high bond energy. We report here a novel palladium-catalyzed C-C bond activation manner of methylenecyclobutanes followed by subsequent Suzuki cross-coupling reaction affording multisubstituted indanes. The tandem reaction process involves intramolecular carbopalladation of double bond, beta-carbon elimination and intermolecular trapping of the transient sigma-alkylpalladium complex with boronic acids. A new TADDOL-derived phosphoramidite ligand bearing fluorine and silicon-based bulky groups is found to be efficient for C-C bond activation of methylenecyclobutanes.
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