期刊
CHEMISTRY LETTERS
卷 40, 期 9, 页码 894-901出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2011.894
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资金
- Grants-in-Aid for Scientific Research [22550092] Funding Source: KAKEN
The palladium-catalyzed cross-coupling reaction between different types of organoboron compounds and various organic halides or triflates in the presence of base provides a powerful and general methodology for the formation of carbon-carbon bonds. The Csp(2)-B compounds (such as aryl- and 1-alkenylboron derivatives) and Csp(3)-B compounds (alkylboron compounds) readily cross-couple with organic electrophiles to give coupled products selectively in high yields. Recently, the Csp-B compounds (1-alkynylboron derivatives) have been also observed to react with organic electrophiles to produce expected cross-coupled products. The overview of some of such coupling reactions is discussed here in this article.
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