Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Martin Newcomb

Showing results (31-40 of 64) with videos related to

Pageof 7
Sort By:
The Journal of Physical Chemistry. A|February 14, 2008
Rate constants for 1,5- and 1,6-hydrogen atom transfer reactions of mono-, di-, and tri-aryl-substituted donors, models for hydrogen atom transfers in polyunsaturated fatty acid radicalsChristopher B DeZutter, John H Horner, Martin Newcomb
Organic & Biomolecular Chemistry|November 10, 2010
Rate constants for cyclizations of α-hydroxy radical clocksChristopher B DeZutter, John H Horner, Martin Newcomb
Chemistry (Weinheim an Der Bergstrasse, Germany)|February 3, 2012
Rate-controlling isomerizations in fatty acid oxidations by a cytochrome P450 compound IZhi Su, Xiaohong Chen, John H Horner, et al.
Journal of the American Chemical Society|April 29, 2004
Solvent polarity effects and limited acid catalysis in rearrangements of model radicals for the methylmalonyl-CoA mutase- and isobutyryl-CoA mutase-catalyzed isomerization reactionsPierre Daublain, John H Horner, Andriy Kuznetsov, et al.
Organic & Biomolecular Chemistry|September 9, 2011
Oxidation of 10-undecenoic acid by cytochrome P450(BM-3) and its Compound I transientXiaohong Chen, Zhi Su, John H Horner, et al.
Biochemistry|February 3, 2009
Kinetic isotope effects in hydroxylation reactions effected by cytochrome P450 compounds I implicate multiple electrophilic oxidants for P450-catalyzed oxidationsXin Sheng, Haoming Zhang, Paul F Hollenberg, et al.
Organic Letters|March 14, 2003
Efficient production of enol ether radical cations by heterolytic cleavage of beta-mesylate radicalsElsa Taxil, Laurent Bagnol, John H Horner, et al.
Journal of the American Chemical Society|May 2, 2003
Carboxylate-substituted radicals from phenylselenide derivatives. Designs on models for coenzyme B12-dependent enzyme-catalyzed rearrangementsNeil Miranda, Pierre Daublain, John H Horner, et al.
Organic Letters|April 14, 2009
Production of a putative iron(V)-oxocorrole species by photo-disproportionation of a bis-corrole-diiron(IV)-mu-oxo dimer: implication for a green oxidation catalystDilusha N Harischandra, Gerald Lowery, Rui Zhang, et al.
Journal of the American Chemical Society|July 4, 2009
Quantitative production of compound I from a cytochrome P450 enzyme at low temperatures. Kinetics, activation parameters, and kinetic isotope effects for oxidation of benzyl alcoholQin Wang, Xin Sheng, John H Horner, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
The Journal of Physical Chemistry. A|February 14, 2008
Rate constants for 1,5- and 1,6-hydrogen atom transfer reactions of mono-, di-, and tri-aryl-substituted donors, models for hydrogen atom transfers in polyunsaturated fatty acid radicalsChristopher B DeZutter, John H Horner, Martin Newcomb
Organic & Biomolecular Chemistry|November 10, 2010
Rate constants for cyclizations of α-hydroxy radical clocksChristopher B DeZutter, John H Horner, Martin Newcomb
Chemistry (Weinheim an Der Bergstrasse, Germany)|February 3, 2012
Rate-controlling isomerizations in fatty acid oxidations by a cytochrome P450 compound IZhi Su, Xiaohong Chen, John H Horner, et al.
Journal of the American Chemical Society|April 29, 2004
Solvent polarity effects and limited acid catalysis in rearrangements of model radicals for the methylmalonyl-CoA mutase- and isobutyryl-CoA mutase-catalyzed isomerization reactionsPierre Daublain, John H Horner, Andriy Kuznetsov, et al.
Organic & Biomolecular Chemistry|September 9, 2011
Oxidation of 10-undecenoic acid by cytochrome P450(BM-3) and its Compound I transientXiaohong Chen, Zhi Su, John H Horner, et al.
Biochemistry|February 3, 2009
Kinetic isotope effects in hydroxylation reactions effected by cytochrome P450 compounds I implicate multiple electrophilic oxidants for P450-catalyzed oxidationsXin Sheng, Haoming Zhang, Paul F Hollenberg, et al.
Organic Letters|March 14, 2003
Efficient production of enol ether radical cations by heterolytic cleavage of beta-mesylate radicalsElsa Taxil, Laurent Bagnol, John H Horner, et al.
Journal of the American Chemical Society|May 2, 2003
Carboxylate-substituted radicals from phenylselenide derivatives. Designs on models for coenzyme B12-dependent enzyme-catalyzed rearrangementsNeil Miranda, Pierre Daublain, John H Horner, et al.
Organic Letters|April 14, 2009
Production of a putative iron(V)-oxocorrole species by photo-disproportionation of a bis-corrole-diiron(IV)-mu-oxo dimer: implication for a green oxidation catalystDilusha N Harischandra, Gerald Lowery, Rui Zhang, et al.
Journal of the American Chemical Society|July 4, 2009
Quantitative production of compound I from a cytochrome P450 enzyme at low temperatures. Kinetics, activation parameters, and kinetic isotope effects for oxidation of benzyl alcoholQin Wang, Xin Sheng, John H Horner, et al.
Pageof 7