Vito Fiandanese

Iron catalyzed cross-coupling reactions of acyl chlorides with Grignard reagents. A mild, general, and convenient synthesis of aliphatic and aromatic ketones.

Vito Fiandanese, Giuseppe Marchese, Virginia Martina et al. · Tetrahedron Letters · 1984 · 123 citations

Chemical Engineering, Cross-coupling Reaction, Engineering +8

A highly efficient synthetic route to ketones through sequential coupling reactions of grignard reagents with -phenyl carbonochloridothioate in the presence of nickel or iron catalysts

Cosimo Cardellicchio, Vito Fiandanese, Giuseppe Marchese et al. · Tetrahedron Letters · 1985 · 86 citations

Efficient Synthetic Route, Chemical Engineering, Cross-coupling Reaction +9

Functionalized ketones by iron mediated reaction of grignard reagents with acyl chlorides

Cosimo Cardellicchio, Vito Fiandanese, Giuseppe Marchese et al. · Tetrahedron Letters · 1987 · 76 citations

Chemical Engineering, Enantioselective Synthesis, Engineering +5

A direct access to α-diones from oxalyl chloride

Francesco Babudri, Vito Fiandanese, Giuseppe Marchese et al. · Tetrahedron Letters · 1995 · 70 citations

Engineering, Oxalyl Chloride, Organic Chemistry +3

One-step synthesis of dialkynyl-1,2-diones and their conversion to fused pyrazines bearing enediyne units

Rüdiger Faust, Christian Weber, Vito Fiandanese et al. · Tetrahedron · 1997 · 61 citations

Engineering, Organic Chemistry, One-step Synthesis +6