References
- Phan, N. T. S.; Sluys, M. V. D.; Jones, C. W. Adv. Synth. Catal. 2006, 348, 609. https://doi.org/10.1002/adsc.200505473
- Yin, L.; Liebscher, J. Chem. Rev. 2007, 107,133. https://doi.org/10.1021/cr0505674
- Lemo, J.; Heuze, K.; Astruc, D. Org. Lett. 2005, 7, 2253. https://doi.org/10.1021/ol050645+
- Schweizer, S.; Becht, J.-M.; Drian, C. L. Org. Lett. 2007, 9, 3777. https://doi.org/10.1021/ol701460z
- Sayah, R.; Glegola, K.; Framery, E.; Dufaud, V. Adv. Synth. Catal. 2007, 349, 373. https://doi.org/10.1002/adsc.200600286
- Jung, J.-Y.; Kim, J.-B.; Taher, A.; Jin, M.-J. Bull. Korean Chem. Soc. 2009, 30, 3082. https://doi.org/10.5012/bkcs.2009.30.12.3082
- Lamblin, M.;Nassar-Hardy, L.; Hierso, J.-C.; Fouquet, E.; Felpin, F.-X. Adv. Synth. Catal. 2010, 352, 33. https://doi.org/10.1002/adsc.200900765
- Jin, M.-J.; Lee, D.-H. Angew. Chem. Int. Ed. 2010, 49, 1119. https://doi.org/10.1002/anie.200905626
- Schweizer, S.; Becht, J.-M.; Drian, C. L. Adv. Synth. Catal. 2007, 349, 1150. https://doi.org/10.1002/adsc.200600503
- Webb, J. D.; MacQuarrie, S.; McEleney, K.; Crudden, C. M. J. Catal. 2007, 252, 97. https://doi.org/10.1016/j.jcat.2007.09.007
- Kohler, K.; Heidenreich, R. G.; Soomro, S. S.; Prockl, S. S. Adv. Synth. Catal. 2008, 350, 2930. https://doi.org/10.1002/adsc.200800575
- Billingsley, K. L.; Buchwald, S. L. Angew. Chem. Int. Ed. 2008, 47, 4695. https://doi.org/10.1002/anie.200801465
- Diebolt, O.; Braunstein, P.; Nolan, S. P.; Cazin, C. S. J. Chem. Commun. 2008, 3190.
- Qiu, H.; Sarkar, S. M.; Lee, D.-H.; Jin, M.-J. Green Chem. 2008, 10, 37. https://doi.org/10.1039/b712624g
- Sawai, K.; Tatumi, R.; Nakahodo, T.; Fujihara, H. Angew. Chem. Int. Ed.2008, 47, 6917. https://doi.org/10.1002/anie.200802174
- Billingsley, K. L.; Buchwald, S. L. Angew. Chem. Int. Ed. 2008, 47, 4695. https://doi.org/10.1002/anie.200801465
- Scheuermann, G. M.; Rumi, L.; Steurer, P.; Bannwarth, W.; Mulhaupt, R. J. Am. Chem. Soc. 2009, 131, 8262. https://doi.org/10.1021/ja901105a
- Peng, Y.-Y.; Liu, J.; Lei, X.; Yin, Z. Green Chem. 2010, 12, 1072. https://doi.org/10.1039/c000739k
- Lysen, M.; Kohler, K. Synlett 2005, 1671.
- Sayah, R.; Glegola, K.; Framery, E.; Dufaud, V. Adv. Synth. Catal. 2007, 349, 373. https://doi.org/10.1002/adsc.200600286
- Schweizer, S.; Becht, J.-M.; Drian, C. L. Org. Lett. 2007,9, 3777. https://doi.org/10.1021/ol701460z
- Lee. D.-H.; Kim, J.-H.; Jun, B.-H.; Kang, H.; Park, J.; Lee, Y.-S. Org. Lett. 2008, 10, 1609. https://doi.org/10.1021/ol8003047
- Komaromi, A.; Novak, Z. Chem. Commun. 2008, 4968.
- Kondoff, I.; Doucet, H.; Santelli, M. J. Mol. Catal. A: Chem. 2007, 269, 110. https://doi.org/10.1016/j.molcata.2007.01.011
- Billingsley, K.; Buchwald, S. L. J. Am. Chem. Soc. 2007, 129, 3358. https://doi.org/10.1021/ja068577p
- Yin, L.; Liebscher, J. Chem. Rev. 2007, 107, 133 https://doi.org/10.1021/cr0505674
- Shi, S.; Zhang, Y. Green Chem. 2008, 10, 868. https://doi.org/10.1039/b803917h
Cited by
- ChemInform Abstract: Highly Active Heterogeneous Palladium Catalyst for the Suzuki Reaction of Heteroaryl Chlorides. vol.42, pp.10, 2011, https://doi.org/10.1002/chin.201110146
- Palladium-Catalyzed C-2 Selective Arylation of Quinolines vol.15, pp.20, 2013, https://doi.org/10.1021/ol402262c
- Recent Applications of Magnetically Recoverable Nanocatalysts in CC and CX Coupling Reactions vol.7, pp.12, 2015, https://doi.org/10.1002/cctc.201403057
- core–shell–shell magnetic nanoparticles: a novel catalyst for the synthesis of imidazole derivatives under solvent-free conditions vol.40, pp.5, 2016, https://doi.org/10.1039/C5NJ02680F
- Placing Ni(II) Ions in Various Positions In/On Layered Double Hydroxides: Synthesis, Characterization and Testing in C-C Coupling Reactions vol.149, pp.10, 2010, https://doi.org/10.1007/s10562-019-02742-6