| 000 | 01621nam a22002777a 4500 | ||
|---|---|---|---|
| 003 | ZW-GwMSU | ||
| 005 | 20250318075148.0 | ||
| 008 | 250318b |||||||| |||| 00| 0 eng d | ||
| 022 | _a09743626 | ||
| 040 |
_aMSU _bEnglish _cMSU _erda |
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| 050 | 0 | 0 | _aQD31 JOU |
| 100 | 1 |
_aSiddiqui, Mujahuddin M. _eauthor |
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| 245 | 1 | 0 |
_aApplication of quinoxaline based diimidazolium salt in palladium catalyzed cross-coupling reactions / _ccreated by Mujahuddin M. Siddiqui, Mohammed Waheed, Sajad A. Bhat and Maravanji S. Balakrishna |
| 264 | 1 |
_aBangalore : _bSpringer, _c2015. |
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| 336 |
_2rdacontent _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdacarrier _avolume _bnc |
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| 440 |
_aJournal of chemical sciences _vVolume 127, number 5, |
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| 520 | 3 | _aThe reaction of 2,3-bis(bromomethyl)quinoxaline with imidazole afforded the quinoxaline bridged diimidazolium salt (1) in good yield. Diimidazolium salt (1) in conjunction with Pd(OAc)2 was employed as a catalyst for C–C cross-coupling reactions. The diimidazolium salt was found to be efficient in catalyzing Suzuki-Miyaura cross-coupling reaction in ethanol under ambient conditions. Moderate to good selectivity of the trans product was observed in the Heck cross-coupling reaction. The molecular structure of 1 was confirmed by single crystal X-ray diffraction study. | |
| 650 |
_aCarbene _vImidazolium salt _xSuzuki-Miyaura coupling |
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| 700 | 1 |
_aWaheed, Mohammed _eco author |
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| 700 | 1 |
_aBhat, Sajad A. _eco author |
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| 700 | 1 |
_aBalakrishna, Maravanji S. _eco author |
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| 856 | _uhttps://doi.org/10.1007/s12039-015-0844-8 | ||
| 942 |
_2lcc _cJA |
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| 999 |
_c169326 _d169326 |
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