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 · 228 citations

Natural Sciences, Chemistry, Bioorganic Chemistry +8

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

Natural Sciences, Chemistry, Analytical Chemistry +5

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

Natural Sciences, Chemistry, Organic Chemistry +13

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

Natural Sciences, Chemistry, Analytical Chemistry +6

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

Natural Sciences, Chemistry, Catalysis +8