Yukihiro Shigeta

A Novel Tandem Michael Addition/Meerwein−Ponndorf−Verley Reduction:  Asymmetric Reduction of Acyclic α,β-Unsaturated Ketones Using A Chiral Mercapto Alcohol

Manabu Node, Kiyoharu Nishide, Yukihiro Shigeta et al. · Journal of the American Chemical Society · 2000 · 106 citations

Chiral Alcohol Reagent, Thiol Group, Engineering +13

Reductive desulfurization using the raney nickel — Sodium hypophosphite combination system without racemization of a secondary alcohol

Kiyoharu Nishide, Yukihiro Shigeta, K. OBATA et al. · Tetrahedron Letters · 1996 · 52 citations

Chemical Engineering, Industrial Chemistry, Engineering +5

Asymmetric 1,7-Hydride Shift:  The Highly Asymmetric Reduction of α,β-Unsaturated Ketones to Secondary Alcohols <i>via</i> a Novel Tandem Michael Addition−Meerwein−Ponndorf−Verley Reduction

Kiyoharu Nishide, Yukihiro Shigeta, K. OBATA et al. · Journal of the American Chemical Society · 1996 · 51 citations

Highly Asymmetric Reduction, Medicinal Chemistry, Engineering +15

A Raney nickel — sodium hypophosphite combination system for reductive desulfurization without racemization of optically active secondary alcohol

Manabu Node, Kiyoharu Nishide, Yukihiro Shigeta et al. · Tetrahedron · 1997 · 48 citations

Chemical Engineering, Engineering, Reductive Desulfurization +5

One‐Step Stereocontrol of Three Contiguous Stereogenic Centers in Acyclic Systems: The Tuning Effect of an Additive in a Tandem Asymmetric Michael Addition and Meerwein–Ponndorf–Verley Reduction

Kiyoharu Nishide, Minoru Ozeki, Hideaki Kunishige et al. · Angewandte Chemie International Edition · 2003 · 32 citations

Suitable Precursors, Natural Product Synthesis, Acyclic Systems +12