D. Edwards

发表

Catalysis by a de novo zinc-mediated protein interface: implications for natural enzyme evolution and rational enzyme engineering.

Brian Kuhlman, Bryan S. Der, Bryan S Der, 2012, Biochemistry.

One‐Pot Carbon Monoxide‐Free Hydroformylation of Internal Olefins to Terminal Aldehydes

C. Crudden, D. Edwards, Katherine C. Yam, 2005 .

Control of NOx in alkaline media with tertiary butyl hydroperoxide

D. Edwards, 1998 .

Catalytic Asymmetric Hydroboration: Recent Advances and Applications in Carbon−Carbon Bond‐Forming Reactions

C. Crudden, D. Edwards, 2003 .

Catalysis by desolvation: the catalytic prowess of SAM-dependent halide-alkylating enzymes.

R. Wolfenden, D. Edwards, D. C. Lohman, 2013, Journal of the American Chemical Society.

On the question of stepwise vs. concerted cleavage of RNA models promoted by a synthetic dinuclear Zn(II) complex in methanol: implementation of a noncleavable phosphonate probe.

D. Edwards, R. S. Brown, W. Tsang, 2010, Organic & biomolecular chemistry.

Dinuclear Zn(II) catalysts as biomimics of RNA and DNA phosphoryl transfer enzymes: changing the medium from water to alcohol provides enzyme‐like rate enhancements

D. Edwards, R. S. Brown, W. Tsang, 2010 .

Dinuclear Zn(II) complex promotes cleavage and isomerization of 2-hydroxypropyl alkyl phosphates by a common cyclic phosphate intermediate.

D. Edwards, Nicholas H Williams, R. S. Brown, 2009, Journal of the American Chemical Society.

Regioselectivity of the rhodium-catalyzed hydroboration of vinyl arenes: electronic twists and mechanistic shifts.

C. Crudden, D. Edwards, Yonek B. Hleba, 2007, Angewandte Chemie.

Toward selective functionalisation of oligosilanes: borane-catalysed dehydrogenative coupling of silanes with thiols.

D. J. Harrison, D. Edwards, R. McDonald, 2008, Dalton transactions.

Experimental investigation into the mechanism of the epoxidation of aldehydes with sulfur ylides.

C. Crudden, D. Edwards, Pedro J Montoya-Peleaz, 2007, Organic letters.

Proton-in-flight mechanism for the spontaneous hydrolysis of N-methyl O-phenyl sulfamate: implications for the design of steroid sulfatase inhibitors.

R. Wolfenden, D. Edwards, 2012, The Journal of organic chemistry.

Study on the transesterification of methyl aryl phosphorothioates in methanol promoted by Cd(II), Mn(II), and a synthetic Pd(II) complex.

D. Edwards, R. S. Brown, A. A. Neverov, 2011, Inorganic chemistry.

Development of metal-ion containing catalysts for the decomposition of phosphorothioate esters.

D. Edwards, R. S. Brown, David R. Edwards, 2013, Biochimica et biophysica acta.

Hydrolysis of N-alkyl sulfamates and the catalytic efficiency of an S-N cleaving sulfamidase.

R. Wolfenden, D. Edwards, D. C. Lohman, 2012, The Journal of organic chemistry.

Dissociative solvolytic cleavage of methyl (ortho-carboxymethyl)aryl phosphate diesters mediated by Yb3+ in methanol gives a 10(12)-fold rate acceleration attributable to leaving group assistance.

D. Edwards, R. S. Brown, A. A. Neverov, 2009, Journal of the American Chemical Society.

Catalytic proficiency: the extreme case of S-O cleaving sulfatases.

Richard Wolfenden, R. Wolfenden, D. Edwards, 2012, Journal of the American Chemical Society.

Mechanistic and computational study of a palladacycle-catalyzed decomposition of a series of neutral phosphorothioate triesters in methanol.

N. Mosey, D. Edwards, R. S. Brown, 2010, Journal of the American Chemical Society.

Leaving group assistance in the La3+-catalyzed cleavage of dimethyl (o-methoxycarbonyl)aryl phosphate triesters in methanol.

D. Edwards, R. S. Brown, G. Garrett, 2009, Journal of the American Chemical Society.

Experimental and computational determination of Brønsted coefficients for equilibrium transfer of the O,O‐dimethyl phosphorothioyl group between oxyanion nucleophiles

N. Mosey, D. Edwards, R. S. Brown, 2012 .

Theoretical and Experimental Studies on the Baeyer−Villiger Oxidation of Ketones and the Effect of α-Halo Substituents

C. Crudden, D. Edwards, F. Grein, 2006 .

A study of the kinetics of La3+-promoted methanolysis of S-aryl methylphosphonothioates: possible methodology for decontamination of EA 2192, the toxic byproduct of VX hydrolysis.

D. Edwards, R. S. Brown, Basab B. Dhar, 2011, Inorganic chemistry.