beta-scission of the N-O bond in alkyl hydroxamate radicals: a fast radical trap.
暂无分享,去创建一个
[1] E. Suárez,et al. SYNTHESIS OF ALDITOLS BY REDUCTIVE RADICAL FRAGMENTATION OF N-PHTHALIMIDO GLYCOSIDES. PREPARATION OF CHIRAL SYNTHETIC INTERMEDIATES , 1999 .
[2] M. Newcomb,et al. PICOSECOND RADICAL KINETICS. RATE CONSTANTS FOR RING OPENINGS OF 2-ARYL-SUBSTITUTED CYCLOPROPYLCARBINYL RADICALS , 1999 .
[3] A. Huang,et al. Synthesis of Tetrahydrofurans by a Tandem Hydrogen Atom Abstraction/Radical Nucleophilic Displacement Sequence , 1999 .
[4] K. Kivirikko,et al. Mechanism-Based Inactivation of the Human Prolyl-4-hydroxylase by 5-Oxaproline-Containing Peptides: Evidence for a Prolyl Radical Intermediate , 1999 .
[5] M. J. Coon,et al. Two distinct electrophilic oxidants effects hydroxylation in cytochrome P-450-catalyzed reactions [20] , 1998 .
[6] A. Clark,et al. Stereoselectivity in amidyl radical cyclisations. Acyl mode cyclisations , 1998 .
[7] K. Kivirikko,et al. Substrate specificity of human prolyl-4-hydroxylase. , 1998, Bioorganic & medicinal chemistry letters.
[8] Hung‐wen Liu,et al. Spiropentylacetyl-CoA, A Mechanism-Based Inactivator of Acyl-CoA Dehydrogenases , 1998 .
[9] N. Castagnoli,et al. Chemical model studies on the monoamine oxidase-B catalyzed oxidation of 4-substituted 1-methyl-1,2,3,6-tetrahydropyridines. , 1997, Bioorganic & medicinal chemistry.
[10] R. Silverman. Radical Ideas about Monoamine Oxidase , 1995 .
[11] P. Mariano,et al. Flavin Chemical Models for Monoamine Oxidase Inactivation by Cyclopropylamines, .alpha.-Silylamines, and Hydrazines , 1995 .
[12] D. Putt,et al. Cytochrome P450-catalyzed hydroxylation of hydrocarbons: kinetic deuterium isotope effects for the hydroxylation of an ultrafast radical clock. , 1994, Biochemistry.
[13] R. Silverman,et al. Evidence against a Nucleophilic Mechanism for Monoamine Oxidase-Catalyzed Amine Oxidation , 1994 .
[14] S. Zard,et al. Iminyl radicals: Part III. Further synthetically useful sources of iminyl radicals. , 1994 .
[15] C. Townsend,et al. Synthesis and reaction of potential alternate substrates and mechanism-based inhibitors of clavaminate synthase. , 1993, Journal of natural products.
[16] M. Lai,et al. Inactivation of medium-chain acyl-CoA dehydrogenase by a metabolite of hypoglycin: characterization of the major turnover product and evidence suggesting an alternative flavin modification pathway , 1993 .
[17] Stephen J. Lippard,et al. Radical clock substrate probes and kinetic isotope effect studies of the hydroxylation of hydrocarbons by methane monooxygenase , 1993 .
[18] M. Lai,et al. New evidence supporting a radical mechanism of the inactivation of general acyl-CoA dehydrogenase by a metabolite of hypoglycin , 1992 .
[19] S. Zard,et al. A new and synthetically useful source of iminyl radicals. , 1992 .
[20] V. Bowry,et al. A radical clock investigation of microsomal cytochrome P-450 hydroxylation of hydrocarbons. Rate of oxygen rebound , 1991 .
[21] C. Schofield,et al. Studies on the mechanism of deacetoxy–deacetylcephalosporin C synthase using cyclopropyl substituted cephalosporin probes , 1991 .
[22] C. Suckling. The Cyclopropyl Group in Studies of Enzyme Mechanism and Inhibition , 1988 .
[23] J. Baldwin,et al. Use of the cyclopropylcarbinyl test to detect a radical-like intermediate in penicillin biosynthesis , 1987 .
[24] J. Walton,et al. The influence of α-trialkylsilyloxy groups on the rate of ring opening of cyclopropylmethyl radicals , 1983 .