Microwave-enhanced cross-coupling reactions involving alkynyltrifluoroborates with aryl bromides

Vitali Coltuclu, Eric Dadush, Abhijit Naravane, George Kabalka

Research output: Contribution to journalArticle

1 Citation (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)1755-1761
Number of pages7
JournalMolecules
Volume18
Issue number2
DOIs
StatePublished - Feb 1 2013

Fingerprint

cross coupling
Cross Reactions
Palladium
Microwaves
Bromides
palladium
bromides
microwaves
Alkynes
Microwave irradiation
alkynes
Materials science
synthesis
materials science
Biological Products
catalysts
Catalysts
irradiation
products

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Microwave-enhanced cross-coupling reactions involving alkynyltrifluoroborates with aryl bromides. / Coltuclu, Vitali; Dadush, Eric; Naravane, Abhijit; Kabalka, George.

In: Molecules, Vol. 18, No. 2, 01.02.2013, p. 1755-1761.

Research output: Contribution to journalArticle

Coltuclu, Vitali ; Dadush, Eric ; Naravane, Abhijit ; Kabalka, George. / Microwave-enhanced cross-coupling reactions involving alkynyltrifluoroborates with aryl bromides. In: Molecules. 2013 ; Vol. 18, No. 2. pp. 1755-1761.
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