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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

249 related items for PubMed ID: 16270992

  • 1. Autoxidation-product-initiated dioxygenases: vanadium-based, record catalytic lifetime catechol dioxygenase catalysis.
    Yin CX, Sasaki Y, Finke RG.
    Inorg Chem; 2005 Nov 14; 44(23):8521-30. PubMed ID: 16270992
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  • 4. Synthesis and characterization of V(V)(3,6-DBSQ)(3,6-DBCat)2, a d(0) metal complex with dioxygenase catalytic activity.
    Morris AM, Pierpont CG, Finke RG.
    Inorg Chem; 2009 Apr 20; 48(8):3496-8. PubMed ID: 19317407
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  • 6. Dioxygenases without requirement for cofactors and their chemical model reaction: compulsory order ternary complex mechanism of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase involving general base catalysis by histidine 251 and single-electron oxidation of the substrate dianion.
    Frerichs-Deeken U, Ranguelova K, Kappl R, Hüttermann J, Fetzner S.
    Biochemistry; 2004 Nov 16; 43(45):14485-99. PubMed ID: 15533053
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  • 8. Iron(III) complexes of tripodal monophenolate ligands as models for non-heme catechol dioxygenase enzymes: correlation of dioxygenase activity with ligand stereoelectronic properties.
    Mayilmurugan R, Visvaganesan K, Suresh E, Palaniandavar M.
    Inorg Chem; 2009 Sep 21; 48(18):8771-83. PubMed ID: 19694480
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  • 9. Vanadium aminophenolates in catechol oxidation: conformity with Finke's common catalyst hypothesis.
    Salonen P, Savela R, Peuronen A, Lehtonen A.
    Dalton Trans; 2021 May 11; 50(18):6088-6099. PubMed ID: 33973597
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  • 10. Mechanism-guided development of VO(salen)X complexes as catalysts for the asymmetric synthesis of cyanohydrin trimethylsilyl ethers.
    Belokon YN, Clegg W, Harrington RW, Maleev VI, North M, Pujol MO, Usanov DL, Young C.
    Chemistry; 2009 May 11; 15(9):2148-65. PubMed ID: 19145602
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  • 11. Monitoring supported-nanocluster heterogeneous catalyst formation: product and kinetic evidence for a 2-step, nucleation and autocatalytic growth mechanism of Pt(0)n formation from H2PtCl6 on Al2O3 or TiO2.
    Mondloch JE, Yan X, Finke RG.
    J Am Chem Soc; 2009 May 13; 131(18):6389-96. PubMed ID: 19379011
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  • 12. Fine-tuning of catalytic properties of catechol 1,2-dioxygenase by active site tailoring.
    Caglio R, Valetti F, Caposio P, Gribaudo G, Pessione E, Giunta C.
    Chembiochem; 2009 Apr 17; 10(6):1015-24. PubMed ID: 19301316
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  • 14. Iron(III)-catecholato complexes as structural and functional models of the intradiol-cleaving catechol dioxygenases.
    Bruijnincx PC, Lutz M, Spek AL, Hagen WR, van Koten G, Gebbink RJ.
    Inorg Chem; 2007 Oct 01; 46(20):8391-402. PubMed ID: 17722878
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  • 16. Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation.
    Widegren JA, Bennett MA, Finke RG.
    J Am Chem Soc; 2003 Aug 27; 125(34):10301-10. PubMed ID: 12926954
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  • 17. Novel iron(III) complexes of sterically hindered 4N ligands: regioselectivity in biomimetic extradiol cleavage of catechols.
    Mayilmurugan R, Stoeckli-Evans H, Palaniandavar M.
    Inorg Chem; 2008 Aug 04; 47(15):6645-58. PubMed ID: 18597419
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  • 18. Catalysis of oxo transfer to prochiral sulfides by oxovanadium(v) compounds that model the active center of haloperoxidases.
    Santoni G, Licini G, Rehder D.
    Chemistry; 2003 Oct 06; 9(19):4700-8. PubMed ID: 14566876
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  • 19. Novel iron(III) porphyrazine complex. Complex speciation and reactions with NO and H2O2.
    Theodoridis A, Maigut J, Puchta R, Kudrik EV, van Eldik R.
    Inorg Chem; 2008 Apr 21; 47(8):2994-3013. PubMed ID: 18351731
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