I. Tomino

Asymmetric synthesis via axially dissymmetric molecules. 6. Rational designing of efficient chiral reducing agents. Highly enantioselective reduction of aromatic ketones by binaphthol-modified lithium aluminum hydride reagents

Ryōji Noyori, I. Tomino, Yoshifumi Tanimoto et al. · Journal of the American Chemical Society · 1984 · 343 citations

Chemical Engineering, Rational Designing, Engineering +9

Asymmetric synthesis via axially dissymmetric molecules. 7. Synthetic applications of the enantioselective reduction by binaphthol-modified lithium aluminum hydride reagents

Ryōji Noyori, I. Tomino, Mitsuhiko Yamada et al. · Journal of the American Chemical Society · 1984 · 303 citations

Chemical Engineering, Enantioselective Reduction, Engineering +13

Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent

Ryōji Noyori, I. Tomino, Yoshifumi Tanimoto · Journal of the American Chemical Society · 1979 · 256 citations

Altmetrics, Chemical Engineering, Environmental Chemistry +13

Asymmetric synthesis via axially dissymetric molecules. 2. A highly efficient synthesis of prostaglandin intermediates possessing the 15S configuration

Ryōji Noyori, I. Tomino, Matsuhiko Nishizawa · Journal of the American Chemical Society · 1979 · 96 citations

Bioorganic Chemistry, Engineering, Altmetric Attention Score +16