Vicky A. Burgess

NADH mimics for the stereoselective reduction of benzoylformates to the corresponding mandelates.

Vicky A. Burgess, Stephen G. Davies, Renato T. Skerlj · Tetrahedron Asymmetry · 1991 · 129 citations

Life Sciences, Biochemistry, Chemistry +7

Selective reaction of glycine residues in hydrogen atom transfer from amino acid derivatives

Vicky A. Burgess, Christopher J. Easton, Michael P. Hay · Journal of the American Chemical Society · 1989 · 77 citations

Natural Sciences, Biochemistry, Chemistry +10

Chiral organometallic NADH mimics: Highly stereoselective reductions of ethyl benzoylformate with a 1,4-dihydronicotinoyl fragment attached to the homochiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)] and possessing a homochiral β-hydroxy-carboxamide at C-5.

Vicky A. Burgess, Stephen G. Davies, Renato T. Skerlj et al. · Tetrahedron Asymmetry · 1992 · 25 citations

Natural Sciences, Biochemistry, Chemistry +9

Chiral organometallic NADH mimics: stereoselective reduction of ethyl benzoylformate utilising the homochiral auxiliary [(η⁵-C₅H₅)Fe(CO)(PPh₃)] at C-3 and a chiral β-hydroxy-carboxamide derived from valinol at C-5

Vicky A. Burgess, Stephen G. Davies, Renato T. Skerlj · Journal of the Chemical Society Chemical Communications · 1990 · 17 citations

Natural Sciences, Biochemistry, Chemistry +6

Stereoselective formation of 4-substituted-1,4-dihydronicotinoyl complexes utilizing the chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)]

R. Paul Beckett, Vicky A. Burgess, Stephen G. Davies et al. · Tetrahedron Letters · 1993 · 14 citations

Natural Sciences, Chemistry, Medicinal Chemistry +7