789 related articles for article (PubMed ID: 20527755)
1. The valence bond way: reactivity patterns of cytochrome P450 enzymes and synthetic analogs.
Shaik S; Lai W; Chen H; Wang Y
Acc Chem Res; 2010 Aug; 43(8):1154-65. PubMed ID: 20527755
[TBL] [Abstract][Full Text] [Related]
2. A valence bond modeling of trends in hydrogen abstraction barriers and transition states of hydroxylation reactions catalyzed by cytochrome P450 enzymes.
Shaik S; Kumar D; de Visser SP
J Am Chem Soc; 2008 Aug; 130(31):10128-40. PubMed ID: 18616242
[TBL] [Abstract][Full Text] [Related]
3. What factors influence the rate constant of substrate epoxidation by compound I of cytochrome P450 and analogous iron(IV)-oxo oxidants?
Kumar D; Karamzadeh B; Sastry GN; de Visser SP
J Am Chem Soc; 2010 Jun; 132(22):7656-67. PubMed ID: 20481499
[TBL] [Abstract][Full Text] [Related]
4. A theory for bioinorganic chemical reactivity of oxometal complexes and analogous oxidants: the exchange and orbital-selection rules.
Usharani D; Janardanan D; Li C; Shaik S
Acc Chem Res; 2013 Feb; 46(2):471-82. PubMed ID: 23210564
[TBL] [Abstract][Full Text] [Related]
5. A proton-shuttle mechanism mediated by the porphyrin in benzene hydroxylation by cytochrome p450 enzymes.
de Visser SP; Shaik S
J Am Chem Soc; 2003 Jun; 125(24):7413-24. PubMed ID: 12797816
[TBL] [Abstract][Full Text] [Related]
6. Propene activation by the oxo-iron active species of taurine/alpha-ketoglutarate dioxygenase (TauD) enzyme. How does the catalysis compare to heme-enzymes?
de Visser SP
J Am Chem Soc; 2006 Aug; 128(30):9813-24. PubMed ID: 16866538
[TBL] [Abstract][Full Text] [Related]
7. Axial ligand effect on the rate constant of aromatic hydroxylation by iron(IV)-oxo complexes mimicking cytochrome P450 enzymes.
Kumar D; Sastry GN; de Visser SP
J Phys Chem B; 2012 Jan; 116(1):718-30. PubMed ID: 22132821
[TBL] [Abstract][Full Text] [Related]
8. Is the ruthenium analogue of compound I of cytochrome p450 an efficient oxidant? A theoretical investigation of the methane hydroxylation reaction.
Sharma PK; De Visser SP; Ogliaro F; Shaik S
J Am Chem Soc; 2003 Feb; 125(8):2291-300. PubMed ID: 12590559
[TBL] [Abstract][Full Text] [Related]
9. To rebound or dissociate? This is the mechanistic question in C-H hydroxylation by heme and nonheme metal-oxo complexes.
Cho KB; Hirao H; Shaik S; Nam W
Chem Soc Rev; 2016 Mar; 45(5):1197-210. PubMed ID: 26690848
[TBL] [Abstract][Full Text] [Related]
10. Valence bond all the way: from the degenerate H-exchange to cytochrome P450.
Shaik S
Phys Chem Chem Phys; 2010 Aug; 12(31):8706-20. PubMed ID: 20574583
[TBL] [Abstract][Full Text] [Related]
11. What factors affect the regioselectivity of oxidation by cytochrome p450? A DFT study of allylic hydroxylation and double bond epoxidation in a model reaction.
de Visser SP; Ogliaro F; Sharma PK; Shaik S
J Am Chem Soc; 2002 Oct; 124(39):11809-26. PubMed ID: 12296749
[TBL] [Abstract][Full Text] [Related]
12. How does the axial ligand of cytochrome P450 biomimetics influence the regioselectivity of aliphatic versus aromatic hydroxylation?
de Visser SP; Tahsini L; Nam W
Chemistry; 2009; 15(22):5577-87. PubMed ID: 19347895
[TBL] [Abstract][Full Text] [Related]
13. What factors influence the ratio of C-H hydroxylation versus C=C epoxidation by a nonheme cytochrome P450 biomimetic?
de Visser SP
J Am Chem Soc; 2006 Dec; 128(49):15809-18. PubMed ID: 17147391
[TBL] [Abstract][Full Text] [Related]
14. Effect of the axial ligand on substrate sulfoxidation mediated by iron(IV)-oxo porphyrin cation radical oxidants.
Kumar D; Sastry GN; de Visser SP
Chemistry; 2011 May; 17(22):6196-205. PubMed ID: 21469227
[TBL] [Abstract][Full Text] [Related]
15. Enhanced reactivities of iron(IV)-oxo porphyrin pi-cation radicals in oxygenation reactions by electron-donating axial ligands.
Kang Y; Chen H; Jeong YJ; Lai W; Bae EH; Shaik S; Nam W
Chemistry; 2009 Oct; 15(39):10039-46. PubMed ID: 19697378
[TBL] [Abstract][Full Text] [Related]
16. What is the active species of cytochrome P450 during camphor hydroxylation? QM/MM studies of different electronic states of compound I and of reduced and oxidized iron-oxo intermediates.
Altun A; Shaik S; Thiel W
J Am Chem Soc; 2007 Jul; 129(29):8978-87. PubMed ID: 17595079
[TBL] [Abstract][Full Text] [Related]
17. Is the bound substrate in nitric oxide synthase protonated or neutral and what is the active oxidant that performs substrate hydroxylation?
de Visser SP; Tan LS
J Am Chem Soc; 2008 Oct; 130(39):12961-74. PubMed ID: 18774806
[TBL] [Abstract][Full Text] [Related]
18. Highly reactive nonheme iron(III) iodosylarene complexes in alkane hydroxylation and sulfoxidation reactions.
Hong S; Wang B; Seo MS; Lee YM; Kim MJ; Kim HR; Ogura T; Garcia-Serres R; Clémancey M; Latour JM; Nam W
Angew Chem Int Ed Engl; 2014 Jun; 53(25):6388-92. PubMed ID: 24820976
[TBL] [Abstract][Full Text] [Related]
19. How do aldehyde side products occur during alkene epoxidation by cytochrome P450? Theory reveals a state-specific multi-state scenario where the high-spin component leads to all side products.
de Visser SP; Kumar D; Shaik S
J Inorg Biochem; 2004 Jul; 98(7):1183-93. PubMed ID: 15219984
[TBL] [Abstract][Full Text] [Related]
20. Two states and two more in the mechanisms of hydroxylation and epoxidation by cytochrome P450.
Hirao H; Kumar D; Thiel W; Shaik S
J Am Chem Soc; 2005 Sep; 127(37):13007-18. PubMed ID: 16159296
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
