Shintani Ryo, Tokunaga Norihito, Doi Hidenori, Hayashi Tamio
Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
J Am Chem Soc. 2004 May 26;126(20):6240-1. doi: 10.1021/ja048825m.
A rhodium-catalyzed asymmetric 1,4-addition reaction has been applied to the synthesis of 2-aryl-4-piperidones. While other conventional nucleophiles fail, organozinc reagents have been successfully utilized for the construction of these useful compounds in very good yield and enantiomeric excess.
铑催化的不对称1,4-加成反应已应用于2-芳基-4-哌啶酮的合成。当其他传统亲核试剂失效时,有机锌试剂已成功用于构建这些有用的化合物,产率和对映体过量均非常好。