Enzymatic resolution of (±)-cis- and (±)-trans-1-aminoindan-2-ol and (±)-cis- and (±)-trans-2-aminoindan-1-ol

Quantitative analyses of biochemical kinetic resolutions of enantiomers

Ching Shih Chen, Yoshitaka Fujimoto, Gary Girdaukas et al. · Journal of the American Chemical Society · 1982 · 2.6K citations

Charles J. Sihcite, Engineering, Chemical Analysis +19

A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa

Romas J. Kazlauskas, Alexandra N. E. Weissfloch, Aviva T. Rappaport et al. · The Journal of Organic Chemistry · 1991 · 944 citations

Lipid Analysis, Candida Rugosa, Alcohol Dehydrogenases +13

L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor.

Joseph P. Vacca, Bruce D. Dorsey, William A. Schleif et al. · Proceedings of the National Academy of Sciences · 1994 · 526 citations · Full text

Immunology, Cell Culture, Pharmacotherapy +19

cis-1-Aminoindan-2-ol in Asymmetric Syntheses

Arun K. Ghosh · Synthesis · 1998 · 75 citations · Full text

Asymmetric Syntheses, Engineering, Biochemistry +5

Chemo-enzymatic synthesis of 1,2- and 1,3- amino-alcohols and their use in the enantioselective reduction of acetophenone and anti-acetophenone oxime methyl ether with borane.

Eric Didier, Bernard Loubinoux, Gerardo H. Ramos Tombo et al. · Tetrahedron · 1991 · 70 citations

Asymmetric Catalysis, Enantioselective Reduction, Enantioselective Synthesis +10