Suzuki Cross-Coupling Reaction of Aryl Halides With Arylboronic Acids Catalysed by Pd(ii)-Nay Zeolite
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Open Access Color
BRONZE
Green Open Access
Yes
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No
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Top 10%
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Average
Abstract
Pd(II)-exchanged NaY zeolite showed high activity in the Suzuki cross-coupling reactions of aryl bromides and iodides without added ligands. The DMF:water ratio, and the type and amount of base were found to be critical for the efficiency of the reaction. The catalyst is reusable after regeneration.
Description
Fields of Science
01 natural sciences, 0104 chemical sciences
Citation
Bulut, H., Artok, L., and Yılmaz, S. (2003). Suzuki cross-coupling reaction of aryl halides with arylboronic acids catalysed by Pd(II)-NaY zeolite. Tetrahedron Letters, 44(2), 289-291. doi:10.1016/S0040-4039(02)02523-6
WoS Q
Q3
Scopus Q
Q3
OpenCitations Citation Count
49
Source
Tetrahedron Letters
Volume
44
Issue
2
Start Page
289
End Page
291
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Scopus : 59
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