Ludovico Ronzini

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

One-step synthesis of ketones from car☐ylic acids and grignard reagents in the presence of a nickel(II)-phosphine catalyst.

Vito Fiandanese, Giuseppe Marchese, Ludovico Ronzini · Tetrahedron Letters · 1983 · 46 citations

Chemical Engineering, Engineering, Grignard Reagents +6

A stereospecific route to olefins through sequential coupling reaction of Grignard reagents with 1-bromo-2-phenylthioethene in the presence of nickel or palladium catalysts

Vito Fiandanese, Giuseppe Marchese, Francesco Naso et al. · Journal of the Chemical Society Chemical Communications · 1982 · 43 citations

Chemical Engineering, Cross-coupling Reaction, Engineering +14