Jacqueline Sandri

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

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

Direct Preparation of (Z,Z)-1,4-Dienic Units with a New C6 Homologating Agent: Synthesis of α-Linolenic Acid

Jacqueline Sandri, Jacques Viala · Synthesis · 1995 · 26 citations

Natural Sciences, Chemistry, Medicinal Chemistry +8

Total stereospecific synthesis of all cis-5,8,11,14,17-eicosapentaenoic acid (EPA)

Jacques Viala, Jacqueline Sandri · Tetrahedron Letters · 1992 · 18 citations

Natural Sciences, Biochemistry, Chemistry +14

A convergent strategy toward linear cis-skipped polyenes

Jacqueline Sandri, Thierry Soto, Jean‐Louis Gras et al. · Tetrahedron Letters · 1997 · 10 citations

Natural Sciences, Chemistry, Combinatorial Chemistry +5