William Smadja

Acyclic Diastereofacial Selection in Intermolecular Radical Reactions Steric<i>vs</i>Electronic Controls

William Smadja · Synlett · 1994 · 127 citations

Acyclic Diastereofacial Selection, Substrate Control, Derivatives +12

Palladium chloride-sodium bicarbonate-catalyzed phenylation of acyclic allylic alcohols. 3. 1,2-Chirality transfer in a Heck reaction via a Wacker-type intermediate

William Smadja, Stanislas Czernecki, Guy Ville et al. · Organometallics · 1987 · 38 citations

Cross-coupling Reaction, Engineering, Heck Reaction +11

Quantitative Description of the Facial Discrimination of Molecules Containing a Prochiral Group by NMR in a Chiral Liquid Crystal

Denis Merlet, A. Loewenstein, William Smadja et al. · Journal of the American Chemical Society · 1998 · 38 citations

Facial Discrimination, Magnetic Resonance, Organic Chemistry +17

RuCl₃–NaOH as a reaǵent for chirality transfer. Synthesis of chiral β-deuteriated ketones by asymmetric induction

William Smadja, Guy Ville, C. Georgoulis · Journal of the Chemical Society Chemical Communications · 1980 · 33 citations

Chemical Engineering, Engineering, Chiral β-Deuteriated Ketones +14

Stereoselective additions of silicon centered radical to α-chiral olefins: A Felkin-Anh stereoelectronic control.

William Smadja, Mohamed Zahouily, Max Malacrìa · Tetrahedron Letters · 1992 · 31 citations

Organic Chemistry, α-Chiral Olefins, Stereoselective Synthesis +5