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1998 biochemical syntheses, microbiological syntheses biochemical syntheses, microbiological syntheses O 0035 15 - 027 Highly Enantioselective Reduction of Symmetrical Diacetylaromatics with Baker’s Yeast. An enantioselective method for the mono- reduction of symmetrical diacetylaromates is developed. — (UCHIYAMA, M.; KATOH, N.; MIMURA, R.; YOKOTA, N.; SHIMOGAICHI, Y.; SHI- MAZAKI, M.; OHTA, A.; Tetrahedron: Asymmetry 8 (1997) 20, 3467-3474; Sch. Pharm., Tokyo Univ. Pharm. Life Sci., Hachioji, Tokyo 192-03, Japan; EN) 1

ChemInform Abstract: Highly Enantioselective Reduction of Symmetrical Diacetylaromatics with Baker′s Yeast

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Page 1: ChemInform Abstract: Highly Enantioselective Reduction of Symmetrical Diacetylaromatics with Baker′s Yeast

1998 biochemical syntheses, microbiological syntheses

biochemical syntheses, microbiological synthesesO 0035

15 - 027Highly Enantioselective Reduction of Symmetrical Diacetylaromaticswith Baker’s Yeast. — An enantioselective method for the mono-reduction of symmetrical diacetylaromates is developed. — (UCHIYAMA,M.; KATOH, N.; MIMURA, R.; YOKOTA, N.; SHIMOGAICHI, Y.; SHI-MAZAKI, M.; OHTA, A.; Tetrahedron: Asymmetry 8 (1997) 20, 3467-3474;Sch. Pharm., Tokyo Univ. Pharm. Life Sci., Hachioji, Tokyo 192-03, Japan; EN)

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