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Volumn 46, Issue 19, 2007, Pages 3567-3570

Metalloenzyme-inspired catalysis: Selective oxidation of primary alcohols with an iridium-aminyl-radical complex

Author keywords

Alcohols; Homogeneous catalysis; Iridium; Oxidation; Radicals

Indexed keywords

ALCOHOLS; ALDEHYDES; CATALYSIS; ENZYMES; IRIDIUM COMPOUNDS; OXIDATION;

EID: 34250804856     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200605170     Document Type: Article
Times cited : (99)

References (36)
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    • 2+ (Cp* = pentamethylcyclopentadienyl; NHC = N-heterocyclic carbine), which reaches turnover numbers (TON) of approximately 7000: F. Hanasaka, K. Fujita, R. Yamaguchi, Organometallics 2005, 24, 3422.
    • 2+ (Cp* = pentamethylcyclopentadienyl; NHC = N-heterocyclic carbine), which reaches turnover numbers (TON) of approximately 7000: F. Hanasaka, K. Fujita, R. Yamaguchi, Organometallics 2005, 24, 3422.
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    • Crystal data for 4: C52H64IrKN 2O7·C4H8O; crystal size: 0.31 x 0.23 × 0.21 mm3, monoclinic, space group P2 1, a, 11.7856(7, b, 24.750(1, c, 17.254(1) Å, β, 95.342(1)°, V, 5010.89 Å3, Z, 4, μ, 2.80 mm-1, T, 200 K, 69595 reflections, 24616 independent, Rint, 0.0304, 1225 parameters, 14 restraints, R1 =0.0302 (for 22911 reflections with I > 2σ (I, wR2, 0.0685 (for all data, GooF, 1.032 (on F 2, max./min. residual electron density: 1.611/-0.502 e Å-3. CCDC-622200 (4) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • -3. CCDC-622200 (4) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data_request/cif.
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    • For the use of quinones as electron-transfer mediators in the ruthenium-catalyzed aerobic oxidation of secondary alcohols, see: G. Csjernyik, A. H. Éll, L. Fadini, B. Pugin, J.-E. Bäckvall, J. Org. Chem. 2002, 67, 1657
    • For the use of quinones as electron-transfer mediators in the ruthenium-catalyzed aerobic oxidation of secondary alcohols, see: G. Csjernyik, A. H. Éll, L. Fadini, B. Pugin, J.-E. Bäckvall, J. Org. Chem. 2002, 67, 1657.
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    • 2-: -1.4 V (vs. the saturated calomel electrode (SCE), aprotic solvents): a) V. P. Vanýsek in CRC Handbook of Chemistry and Physics, 87th ed., CRC, Boca Raton, 2006, pp. 8-32; http://www.hbcpnetbase.com;
    • 2-: -1.4 V (vs. the saturated calomel electrode (SCE), aprotic solvents): a) V. P. Vanýsek in CRC Handbook of Chemistry and Physics, 87th ed., CRC, Boca Raton, 2006, pp. 8-32; http://www.hbcpnetbase.com;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.