This review deals with the metal promoted asymmetric ring opening of achiral epoxides using achiral carbon-, nitrogen-, oxygen-, sulphur- and halogen-containing nucleophiles. The use of chiral bases in the asymmetric deprotonation of achiral epoxides yields chiral allylic alcohols. Finally, kinetic resolution of racemic epoxides can be achieved using chiral metal complexes.
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Univ Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, JapanUniv Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, Japan
Azoulay, S
Manabe, K
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Univ Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, JapanUniv Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, Japan
Manabe, K
Kobayashi, S
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Univ Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, JapanUniv Tokyo, HFRE Div, ERATO, Grad Sch Pharmaceut Sci,JST,Bunkyo Ku, Tokyo 1130033, Japan