Activation of ketene silyl acetals by 10-methylacridinium perchlorate: a novel catalysis in mukaiyama reaction

THE MICHAEL TYPE REACTION OF O-SILYLATED KETENE ACETALS WITH α,β-UNSATURATED CARBONYL COMPOUNDS PROMOTED BY TITANIUM TETRACHLORIDE

Kazuhiko Saigo, Masaaki Osaki, Teruaki Mukaiyama · Chemistry Letters · 1976 · 88 citations

Natural Sciences, Chemistry, Organic Chemistry +3

Organotin triflate promoted carbonyl activation. Does acetalization deactivate or activate carbonyl groups?

Tsuneo Sato, Junzo Otera, Hitosi Nozaki · Journal of the American Chemical Society · 1990 · 84 citations

Natural Sciences, Biochemistry, Chemistry +8

Selective one-electron reduction of a cationic substrate, 10-methylacridinium ion, by Group IVA dimetals, Me3SnMMe3 (M = tin, germanium, silicon), via radical chain reactions

Shunichi Fukuzumi, Toshiaki Kitano, Kunio Mochida · Journal of the American Chemical Society · 1990 · 63 citations

Natural Sciences, Chemistry, Catalysis +8

Organotin triflates as functional lewis acids. A new entry to simple and efficient robinson annulation

Tsuneo Sato, Yoshiyuki Wakahara, Junzo Otera et al. · Tetrahedron Letters · 1990 · 50 citations

Natural Sciences, Chemistry, Organic Chemistry +3

Electrogenerated Acid-Catalyzed Reactions of Acetals, Aldehydes, and Ketones with Organosilicon Compounds, Leading to Aldol Reactions, Allylations, Cyanations, and Hydride Additions

Sigeru Torii, Tsutomu Inokuchi, Sadahito Takagishi et al. · Bulletin of the Chemical Society of Japan · 1987 · 38 citations · Full text

Natural Sciences, Chemistry, Catalysis +13