Molecules 2013, 18(2), 1755-1761; doi:10.3390/molecules18021755
Article

Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides

Departments of Chemistry and Radiology, University of Tennessee, Knoxville, TN 37996, USA
* Author to whom correspondence should be addressed.
Received: 21 December 2012; in revised form: 1 January 2013 / Accepted: 12 January 2013 / Published: 29 January 2013
(This article belongs to the Special Issue Organoboron Chemistry)
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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 catalyst has been developed using microwave irradiation. The microwave reactions are rapid and efficient.
Keywords: organotrifluoroborates; alkynes; microwave; coupling reactions

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MDPI and ACS Style

Coltuclu, V.; Dadush, E.; Naravane, A.; Kabalka, G.W. Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides. Molecules 2013, 18, 1755-1761.

AMA Style

Coltuclu V, Dadush E, Naravane A, Kabalka GW. Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides. Molecules. 2013; 18(2):1755-1761.

Chicago/Turabian Style

Coltuclu, Vitali; Dadush, Eric; Naravane, Abhijit; Kabalka, George W. 2013. "Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides." Molecules 18, no. 2: 1755-1761.

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