Hidetaka Yatagai

Lewis acid mediated reactions of organocopper reagents. Entrainment in the conjugate addition to .alpha.,.beta.-unsaturated ketones, esters, and acids via the RCu.cntdot.BF3 system

Yoshinori Yamamoto, Sinichi Yamamoto, Hidetaka Yatagai et al. · The Journal of Organic Chemistry · 1982 · 227 citations

Novel Organocatalysts, Engineering, Biochemistry +14

Erythro-selective addition of crotyltrialkyltins to aldehydes regardless of the geometry of the crotyl unit. Stereoselection independent of the stereochemistry of precursors

Yoshinori Yamamoto, Hidetaka Yatagai, Yoshinori Naruta et al. · Journal of the American Chemical Society · 1980 · 215 citations

Crotyl Unit, Enantioselective Synthesis, Bioorganic Chemistry +10

Stereo- and regiocontrol of acyclic systems via the lewis acid mediated reaction of allylic stannanes with aldehydes

Yoshinori Yamamoto, Hidetaka Yatagai, Yuji Ishihara et al. · Tetrahedron · 1984 · 171 citations

Cross-coupling Reaction, Engineering, Acyclic Systems +9

A new procedure for the stereoselective synthesis of (Z)-2-alkenylsilanes and -tins and their application to erythro-selective synthesis of .beta.-alkyl alcohol derivatives

Hidetaka Yatagai, Yoshinori Yamamoto, Kazuhiro Maruyama · Journal of the American Chemical Society · 1980 · 105 citations

Derivative (Chemistry), Donut Icon, Natural Sciences +12

Lewis acid mediated reactions of organocopper reagents. A remarkably enhanced regioselective .gamma.-attack of allylic halides and direct alkylation of allylic alcohols via RCu.cntdot.BF3 system

Yoshinori Yamamoto, Shin‐ichi Yamamoto, Hidetaka Yatagai et al. · Journal of the American Chemical Society · 1980 · 100 citations

Halogenation, Cross-coupling Reaction, Engineering +12