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Authors = George W. Kabalka

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7 pages, 195 KiB  
Article
Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
by Vitali Coltuclu, Eric Dadush, Abhijit Naravane and George W. Kabalka
Molecules 2013, 18(2), 1755-1761; https://doi.org/10.3390/molecules18021755 - 29 Jan 2013
Cited by 2 | Viewed by 4392
Abstract
Palladium-catalyzed alkynylation has emerged as one of the most reliable methods for the synthesis of alkynes which are often used in natural product syntheses and material science. An efficient method for coupling alkynyltrifluoroborates with various aryl bromides in the presence of a palladium [...] Read more.
Palladium-catalyzed alkynylation has emerged as one of the most reliable methods for the synthesis of alkynes which are often used in natural product syntheses and material science. An efficient method for coupling alkynyltrifluoroborates with various aryl bromides in the presence of a palladium catalyst has been developed using microwave irradiation. The microwave reactions are rapid and efficient. Full article
(This article belongs to the Special Issue Organoboron Chemistry)
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