Baker’s Yeast Mediated Bioreduction of Prochiral Ketones Having 6-(4-Oxo-1,3-dioxinyl) Group
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/6/19_6_901/_pdf
Reference14 articles.
1. Specification of the stereospecificity of some oxido-reductases by diamond lattice sections
2. Microbial Asymmetric Catalysis?Enantioselective Reduction of Ketones [New Synthetic Methods (45)]
3. 1,3-dioxin-4-ones as versatile intermediates for organic synthesis
4. Synthesis of 1,3-dioxin-4-ones and their use in synthesis.
5. Synthesis of 1,3-dioxin-4-ones and their use in synthesis. Part XXII. A novel synthetic method for tetronic acids from 1,3-dioxin-4-ones via intra- or intermolecular ketene trapping.
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3. β-Keto-dioxinones and β,δ-Diketo-dioxinones in Biomimetic Resorcylate Total Synthesis;Accounts of Chemical Research;2015-02-17
4. Asymmetric reduction of 2,2-dimethyl-6-(2-oxoalkyl/oxoaryl)-1,3-dioxin-4-ones and application to the synthesis of (+)-yashabushitriol;Tetrahedron Letters;2013-12
5. ChemInform Abstract: Synthesis of 1,3-Dioxin-4-ones and Their Use in Synthesis. Part 24. Bakers′ Yeast-Mediated Bioreduction of Prochiral Ketones Having 6-(4- Oxo-1,3-dioxinyl) Group.;ChemInform;2010-08-22
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