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Crabtree's catalyst (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Crabtree's catalyst" in English language version.

refsWebsite
Global rank English rank
17doi.org
2nd place
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1illinois.edu
1,349th place
866th place
1nih.gov
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1web.archive.org
1st place
1st place
1massey.ac.nz
low place
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doi.org

  • Crabtree, R. H. (2001). "(1,5-Cyclooctadiene)(tricyclohexylphosphine)(pyridine)iridium(I) Hexafluorophosphate". e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rc290m.pub4 (inactive 31 January 2024).{{cite encyclopedia}}: CS1 maint: DOI inactive as of January 2024 (link)
  • Robert H. Crabtree (1979). "Iridium compounds in catalysis". Acc. Chem. Res. 12 (9): 331–337. doi:10.1021/ar50141a005.
  • Brown, J. M. (1987). "Directed Homogeneous Hydrogenation". Angew. Chem. Int. Ed. 26 (3): 190–203. doi:10.1002/anie.198701901.
  • Crabtree, R. H.; Morris, G. E. (1977). "Some diolefin complexes of Iridium(I) and a trans-Influence Series for the Complexes [IrCl(cod)L]". J. Organomet. Chem. 135 (3): 395–403. doi:10.1016/S0022-328X(00)88091-2.
  • Xu, Yingjian; Mingos, D. Michael P.; Brown, John M. (2008). "Crabtree's catalyst revisited; Ligand effects on stability and durability". Chem. Comm. 2008 (2): 199–201. doi:10.1039/b711979h. PMID 18092086.
  • Crabtree, R.; Felkin, H.; Morris, G. (1977). "Cationic iridium diolefin complexes as alkene hydrogenation catalysts and the isolation of some related hydrido complexes". Journal of Organometallic Chemistry. 141 (2): 205–215. doi:10.1016/S0022-328X(00)92273-3.
  • Schou, S. (2009). "The effect of adding Crabtree's catalyst to rhodium black in direct hydrogen isotope exchange reactions". Journal of Labelled Compounds and Radiopharmaceuticals. 52 (9): 376–381. doi:10.1002/jlcr.1612.
  • Valsborg, J.; Sorensen, L.; Foged, C. (2001). "Organoiridium catalysed hydrogen isotope exchange of benzamide derivatives". Journal of Labelled Compounds and Radiopharmaceuticals. 44 (3): 209–214. doi:10.1002/jlcr.446.
  • Hesk, D.; Das, P.; Evans, B. (1995). "Deuteration of acetanilides and other substituted aromatics using [Ir(COD)(Cy3P)(Py)]PF6 as catalyst". Journal of Labelled Compounds and Radiopharmaceuticals. 36 (5): 497–502. doi:10.1002/jlcr.2580360514.
  • Thompson, H.; Naipawer, R. (1973). "Stereochemical control of reductions. III. Approach to group haptophilicities". Journal of the American Chemical Society. 95 (19): 6379–6386. doi:10.1021/ja00800a036.
  • Brown, J. (1987). "Directed Homogeneous Hydrogenation [New Synthetic Methods (65)]". Angew. Chem. Int. Ed. Engl. 26 (3): 190–203. doi:10.1002/anie.198701901.
  • Schultz, A.; McCloskey, P. (1985). "Carboxamide and carbalkoxy group directed stereoselective iridium-catalyzed homogeneous olefin hydrogenations". Journal of Organic Chemistry. 50 (26): 5905–5907. doi:10.1021/jo00350a105.
  • Crabtree, R. H.; Davis, M. W. (1986). "Directing effects in homogeneous hydrogenation with [Ir(cod)(PCy3)(py)]PF6". J. Org. Chem. 51 (14): 2655–2661. doi:10.1021/jo00364a007.
  • Crabtree, R.; Davis, M. (1983). "Occurrence and origin of a pronounced directing effect of a hydroxyl group in hydrogenation with [Ir(cod)P(C6H11)3(py)]PF6". Organometallics. 2 (5): 681–682. doi:10.1021/om00077a019.
  • Schrock, R.; Osborn, J. A. (1976). "Catalytic hydrogenation using cationic rhodium complexes. I. Evolution of the catalytic system and the hydrogenation of olefins". Journal of the American Chemical Society. 98 (8): 2134–2143. doi:10.1021/ja00424a020.
  • Osborn, J.; Shapley, J. (1970). "Rapid intramolecular rearrangements in pentacoordinate transition metal compounds. Rearrangement mechanism of some fluxional iridium(I) complexes". Journal of the American Chemical Society. 92 (23): 6976–6978. doi:10.1021/ja00726a047.
  • Young, J.; Wilkinson, G. (1966). "The preparation and properties of tris(triphenylphosphine)halogenorhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivatives". J. Chem. Soc. A. 1966: 1711. doi:10.1039/J19660001711.

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