123261-65-4Relevant articles and documents
A highly chemo- and stereoselective synthesis of β-keto esters via a polymer-supported lipase catalyzed transesterfication
Cordova,Janda
, p. 1906 - 1909 (2001)
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Highly selective resolution of secondary alcohols and acetoacetates with lipases and diketene in organic media
Suginaka, Kaoru,Hayashi, Yoshiyuki,Yamamoto, Yukio
, p. 1153 - 1158 (2007/10/03)
By the catalysis of lipases, racemic 1-phenylethanol 1a is reacted with diketene in isopropyl ether at room temperature to give (S)-1a (R1 = Me, R2 = Ph, 36%, 99% ee) and (R)-1-phenylethyl acetoacetate 2a (51%, 77% ee). The strategy was also successfully applied to racemic 1-(1-naphthyl)ethanol 1b, 1-(2-naphthyl)ethanol 1c, 1-phenyl-2-propanol 1d, 1,2,3,4-tetrahydro-1-naphthol 1e, and 2-octanol 1f with high E-values up to > 100.