Geoffrey G. Cox

Diastereoselectivity in the O-H Insertion Reactions of Rhodium Carbenoids Derived from Phenyldiazoacetates of Chiral Alcohols. Preparation of .alpha.-Hydroxy and .alpha.-Alkoxy Esters

Enrique Aller, David S. Brown, Geoffrey G. Cox et al. · The Journal of Organic Chemistry · 1995 · 77 citations

Natural Sciences, Chemistry, Analytical Chemistry +7

Rhodium-carbenoid mediated O-H insertion reactions. O-H insertion vs. H-abstraction and effect of catalyst

Geoffrey G. Cox, David J. Miller, Christopher J. Moody et al. · Tetrahedron · 1994 · 71 citations

Natural Sciences, Chemistry, Catalysis +13

Chemoselectivity of rhodium carbenoids. A comparison of the selectivity for OH insertion reactions or carbonyl ylide formation versus aliphatic and aromatic CH insertion and cyclopropanation

Geoffrey G. Cox, Christopher J. Moody, David J. Austin et al. · Tetrahedron · 1993 · 56 citations

Natural Sciences, Chemistry, Organic Chemistry +11

Glycosylated dihydrochalcones as potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitors

Joseph Dudash, Xiaoyan Zhang, Roxanne E. Zeck et al. · Bioorganic & Medicinal Chemistry Letters · 2004 · 41 citations · Full text

Pharmacy, Medicinal Chemistry, Pharmacology +8

Synthesis of homochiral α-amino acids by reductive amination of α-ketoacids via 3-substituted- 5-phenyl-3,4-dehydromorpholin-2-ones: Synthesis of (S)- and (R)-2-aminobutanoic acid

Geoffrey G. Cox, Laurence M. Harwood · Tetrahedron Asymmetry · 1994 · 35 citations

Natural Sciences, Chemistry, Medicinal Chemistry +11