dc.contributor.author |
Yılmaz, Ülkü |
|
dc.contributor.author |
Şireci, Nihat |
|
dc.contributor.author |
Deniz, Selma |
|
dc.contributor.author |
Küçükbay, Hasan |
|
dc.date.accessioned |
2022-04-04T11:12:18Z |
|
dc.date.available |
2022-04-04T11:12:18Z |
|
dc.date.issued |
2010 |
|
dc.identifier.issn |
0268-2605 |
|
dc.identifier.uri |
http://dspace.adiyaman.edu.tr:8080/xmlui/handle/20.500.12414/2716 |
|
dc.description.abstract |
A mixture of bis-benzimidazole salts (1-7), Pd(OAc)(2) and K(2)CO(3) in DMF-H(2)O catalyzes, in high yield, the Suzuki and Heck cross-coupling reactions assisted by microwave irradiation in a short time. In particular, the yields of the Heck and Suzuki reactions with aryl bromides were found to be nearly quantative. The synthesized bis-benzimidazole salts (1-7) were identified by (1)H-(13)C NMR, IR spectroscopic methods and micro analysis. Copyright (C) 2010 John Wiley & Sons, Ltd. |
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dc.language.iso |
en |
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dc.publisher |
Wiley |
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dc.subject |
Bis-benzimidazole salt |
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dc.subject |
Carbene |
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dc.subject |
Palladium catalysis |
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dc.subject |
Coupling reaction |
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dc.subject |
Heck coupling |
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dc.subject |
Suzuki coupling |
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dc.subject |
Microwave |
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dc.title |
Synthesis and microwave-assisted catalytic activity of novel bis-benzimidazole salts bearing furfuryl and thenyl moieties in Heck and Suzuki cross-coupling reactions |
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dc.type |
Article |
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dc.contributor.authorID |
0000-0002-2806-4781 |
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dc.contributor.authorID |
0000-0003-2608-5893 |
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dc.contributor.authorID |
0000-0002-7180-9486 |
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dc.contributor.department |
Inonu Univ, Fac Sci & Arts, Dept Chem |
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dc.contributor.department |
Adiyaman Univ, Fac Sci & Arts, Dept Chem |
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dc.identifier.endpage |
420 |
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dc.identifier.issue |
5 |
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dc.identifier.startpage |
414 |
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dc.identifier.volume |
24 |
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dc.source.title |
Applied Organometallic Chemistry |
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