Jacques Viala

Syntheses of all-(Z)-5,8,11,14,17-Eicosapentaenoic Acid and all-(Z)-4,7,10,13,16,19-Docosahexaenoic Acid from (Z)-1,1,6,6-tetraisopropoxy-3-hexene

Jacqueline Sandri, Jacques Viala · The Journal of Organic Chemistry · 1995 · 42 citations

Natural Sciences, Biochemistry, Chemistry +8

Clean and Efficient Oxidation of Homoallylic and Homopropargylic Alcohols into β,γ-Unsaturated Aldehydes by The Dess-Martin Periodinane

Laurence Wavrin, Jacques Viala · Synthesis · 2002 · 36 citations

Natural Sciences, Chemistry, Catalysis +4

Total synthesis of the cytochrome P-450 epoxygenase metabolites 5(R),6(S)-, 5(S),6(R)-, and 14(R),15(S)-epoxyeicosatrienoic acid (EET) and hydration products 5(R),6(R)- and 14(R),15(R)-dihydroxyeicosatrienoic acid (DHET)

Christine A. Moustakis, Jacques Viala, Jorge H. Capdevila et al. · Journal of the American Chemical Society · 1985 · 35 citations

Life Sciences, Biochemistry, Chemistry +8

Three-Carbon Homologating Agent: New Preparation of (3,3-Diisopropoxypropyl)triphenylphosphonium Bromide

Jacques Viala, Maurice Santelli · Synthesis · 1988 · 34 citations

Natural Sciences, Chemistry, Organic Chemistry +5

Convenient Conversion of<i>cis</i>-Homoallylic Alcohols into Corresponding Bromides with Ph₃PBr₂

Jacqueline Sandri, Jacques Viala · Synthetic Communications · 1992 · 29 citations

Natural Sciences, Chemistry, Green Chemistry +4