Sodium bis(2-methoxyethoxy)(1,1,1,3,3,3-hexafluoro-2-propoxy)aluminum hydride, a new stereoselective reducing agent in a carbacyclin synthesis

A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses

E. J. Corey, Raman K. Bakshi, Saizo Shibata et al. · Journal of the American Chemical Society · 1987 · 864 citations

Natural Sciences, Chemistry, Catalysis +15

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

Natural Sciences, Chemistry, Catalysis +11

General method for determining absolute configuration of acyclic allylic alcohols

Nina C. Gonnella, Koji Nakanishi, Victor S. Martı́n et al. · Journal of the American Chemical Society · 1982 · 115 citations

Natural Sciences, Chemistry, Analytical Chemistry +6

Mechanism of lithium aluminum hydride reduction of ketones. Kinetics of reduction of mesityl phenyl ketone

E. C. Ashby, James Boone · Journal of the American Chemical Society · 1976 · 59 citations

Natural Sciences, Biochemistry, Chemistry +7

Facile synthesis of 6a-carbaprostaglandin i2

Yoshitaka Konishi, Masanori Kawamura, Yoichi Iguchi et al. · Tetrahedron · 1981 · 20 citations

Pharmacy, Medicinal Chemistry, Pharmacology +4