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Synthesis of chiral epoxy alcohols by use of baker's yeast

✍ Scribed by Mitsuhiro Takeshita; Nami Akutsu

Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
238 KB
Volume
3
Category
Article
ISSN
0957-4166

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πŸ“œ SIMILAR VOLUMES

Baker's yeast mediated preparation of ca
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Baker's yeast mediated reduction of the cc-acetoxy ketones (l)-( 2) proceeds with high enantio-and stereoselectivity to give the anti carbinols ($)-( 6), ea:ily converted into the masked chiral deoxy sugars ( 12)-( 14), --from which E-and k-deoxyzugars have been obtained. Carbohydrates are now bein

Asymmetric synthesis of a nitroalkane by
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✍ Yasushi Kawai; Yoshikazu Inaba; Motoko Hayashi; Norihiro Tokitoh πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 50 KB

Two kinds of novel nitroalkene reductases were isolated from baker's yeast. Reduction of a trisubstituted nitroalkene by these reductases afforded the corresponding nitroalkane with excellent enantioselectivity, moderate diastereoselectivity, and in good yield.