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Stereoselective reduction of 2-substituted cyclohexanones bySaccharo-mycescerevisiae

✍ Scribed by Marie Zarevúcka; Pavla Sochůrková; Zdeněk Wimmer; David Šaman


Book ID
111538865
Publisher
Springer Netherlands
Year
2003
Tongue
English
Weight
89 KB
Volume
25
Category
Article
ISSN
0141-5492

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✍ Michail N. Elinson; Sergey K. Feducovich; Dmitry E. Dmitriev; Alexander S. Dorof 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 62 KB

Electrolysis of 4-substituted cyclohexanones in methanol in the presence of sodium halides in an undivided cell results in the stereoselective formation of cis-5-substituted-2,2-dimethoxycyclohexanols in 70-80% yield.