A PRACTICAL AND STEREOSELECTIVE REDUCTION OF 3-KETO-2-METHYL ESTERS OR 3-KETO-2-METHYL AMIDES INTO ERYTHRO-3-HYDROXY-2-METHYL ESTERS OR ERYTHRO-3-HYDROXY-2-METHYL AMIDES WITH NABH4 CATALYZED BY MNCL2
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FUJII, H
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KYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPANKYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPAN
FUJII, H
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OSHIMA, K
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KYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPANKYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPAN
OSHIMA, K
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UTIMOTO, K
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KYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPANKYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPAN
UTIMOTO, K
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[1] KYOTO UNIV,FAC ENGN,DEPT IND CHEM,SAKYO KU,KYOTO 606,JAPAN
Erythro-3-hydroxy-2-methylpropionates or erythro-3-hydroxy-2-methylpropionamides were prepared with high stereoselectivity by NaBH4 reduction of the corresponding 3-keto esters or 3-keto amides in the presence of a catalytic amount of MnCl2.