Zobrazeno 1 - 10
of 75
pro vyhledávání: '"35"'
Autor:
R. Adam Kinney, Bo Zhang, Rebecca L. McNaughton, Russ Hille, Muralidharan Shanmugam, Brian M. Hoffman
Publikováno v:
Journal of the American Chemical Society. 132:14015-14017
The formaldehyde-inhibited Mo(V) state of xanthine oxidase (I) has been studied for four decades, yet it has not proven possible to distinguish unequivocally among the several structures proposed for this form. The uniquely large isotropic hyperfine
Publikováno v:
Journal of the American Chemical Society. 123(11)
Xanthine oxidase is a molybdenum-containing enzyme that catalyzes the hydroxylation of xanthine and a wide variety of other aromatic heterocycles. In the course of the reaction with xanthine and substrates such as 2-hydroxy-6-methylpurine (HMP), the
Autor:
Rodgers ZL; Department of Chemistry, ‡Division of Chemical Biology and Medicinal Chemistry, and § Department of Pharmacology, University of North Carolina , Chapel Hill, North Carolina 27599, United States., Hughes RM, Doherty LM, Shell JR, Molesky BP, Brugh AM, Forbes MD, Moran AM, Lawrence DS
Publikováno v:
Journal of the American Chemical Society [J Am Chem Soc] 2015 Mar 11; Vol. 137 (9), pp. 3372-8. Date of Electronic Publication: 2015 Feb 27.
Autor:
W. W. Schloman, Harry Morrison
Publikováno v:
Journal of the American Chemical Society. 99:3342-3345
Autor:
Y. Maeda, K. U. Ingold
Publikováno v:
Journal of the American Chemical Society. 102:328-331
A search for a dialkylaminyl radical which rearranges at a rate suitable for study by kinetic EPR spectroscopy has shown that cyclobutyl-n-propylaminyl is such a species. This radical undergoes ring opening, and the rate constant for this process can
Publikováno v:
Journal of the American Chemical Society. 105:7337-7345
Studies have been conducted on the ground-state and excited-state solvolyses of the isomeric 7,8-dichloro derivatives of benzonaphthobicyclo(2.2.2)octadiene and benzoveratrobicyclo(2.2.2)octadiene. The silver ion assisted ground-state reactions proce
Publikováno v:
Journal of the American Chemical Society. 103:5949-5951
Publikováno v:
Journal of the American Chemical Society. 106:2483-2483
Autor:
Olshansky L; Department of Chemistry, Massachusetts Institute of Technology , 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.; Department of Chemistry and Chemical Biology, Harvard University , 12 Oxford St., Cambridge, Massachusetts 02138, United States., Stubbe J; Department of Chemistry, Massachusetts Institute of Technology , 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States., Nocera DG; Department of Chemistry and Chemical Biology, Harvard University , 12 Oxford St., Cambridge, Massachusetts 02138, United States.
Publikováno v:
Journal of the American Chemical Society [J Am Chem Soc] 2016 Feb 03; Vol. 138 (4), pp. 1196-205. Date of Electronic Publication: 2016 Jan 21.
Autor:
Bettinger, Holger F.1 holger.bettinger@rub.de, Bornemann, Holger1
Publikováno v:
Journal of the American Chemical Society. 8/30/2006, Vol. 128 Issue 34, p11128-11134. 7p. 9 Diagrams, 1 Chart, 4 Graphs.