Tetrahedron: Asymmetry

Enantioselective synthesis of 2-hydroxy-1-indanone, a key precursor of enantiomerically pure 1-amino-2-indanol

H Kajiro, S Mitamura, A Mori, T Hiyama

Index: Kajiro, Hiroshi; Mitamura, Shu-Ichi; Mori, Atsunori; Hiyama, Tamejiro Tetrahedron Asymmetry, 1998 , vol. 9, # 6 p. 907 - 910

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Citation Number: 32

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Enantiomerically pure (R)- or (S)-2-hydroxy-1-indanone was synthesized by enzymatic kinetic resolution of racemic 2-acetoxy-1-indanone through hydrolysis or transesterification. ... Enantiomerically pure 1-amino-2-indanol 1 is a key precursor of the chiral ligand[1]2 and the chiral auxiliary[2]3 ...