Issue 18, 1994

Katsuki–Sharpless asymmetric epoxidation of alkenylethylene glycols: the origin of inverted stereoselection

Abstract

The Katsuki–Sharpless asymmetric epoxidation of linear and cyclic alkenylethylene glycols has led to a conclusion that the origin of the inverted stereoselection is due to the simultaneous coordination between both hydroxy groups of the glycol substrates and both titanium atoms in the Ti2(tartrate)2 complex.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 2197-2199

Katsuki–Sharpless asymmetric epoxidation of alkenylethylene glycols: the origin of inverted stereoselection

T. Yoshimitsu and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1994, 2197 DOI: 10.1039/C39940002197

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