David Gueyrard

1,3-Dipolar cycloaddition reactions on carbohydrate-based templates: synthesis of spiro-isoxazolines and 1,2,4-oxadiazoles as glycogen phosphorylase inhibitors

Mahmoud Benltifa, Sébastien Vidal, David Gueyrard et al. · Tetrahedron Letters · 2006 · 83 citations

Combinatorial Chemistry, Medicinal Chemistry, Diversity Oriented Synthesis +8

Formation of glucoraphanin by chemoselective oxidation of natural glucoerucin: A chemoenzymatic route to sulforaphane

Renato Iori, R. Bernardi, David Gueyrard et al. · Bioorganic & Medicinal Chemistry Letters · 1999 · 80 citations

Biosynthesis, Chemoenzymatic Route, Engineering +11

Glucose-based spiro-isoxazolines: A new family of potent glycogen phosphorylase inhibitors

Mahmoud Benltifa, Joseph M. Hayes, Sébastien Vidal et al. · Bioorganic & Medicinal Chemistry · 2009 · 61 citations · Full text

Medicinal Chemistry, New Family, Aldo-keto Reductase +10

Synthesis of Methylene Exoglycals Using a Modified Julia Olefination

David Gueyrard, Rose Haddoub, A. Y. Salem et al. · Synlett · 2005 · 55 citations

Sugar-derived Lactones, Engineering, Alkene Metathesis +12

Synthesis of enol ethers from lactones using modified Julia olefination reagents: application to the preparation of tri- and tetrasubstituted exoglycals

Benjamin Bourdon, Matthieu Corbet, Patrice Fontaine et al. · Tetrahedron Letters · 2007 · 48 citations

Tetrasubstituted Exoglycals, Enol Ethers, Organic Chemistry +6