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Enantio-, Regio-, and Chemoselective Reduction of Aromatic α-Diketones by Baker’s Yeast

✍ Scribed by Nosrat O. Mahmoodi; Hussin G. Mohammadi


Publisher
Springer Vienna
Year
2003
Tongue
English
Weight
75 KB
Volume
134
Category
Article
ISSN
0026-9247

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📜 SIMILAR VOLUMES


Bakers′ Yeast Reduction of α-Diketones:
✍ P. Besse; J. Bolte; A. Fauve; H. Veschambre 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 537 KB

Optically pure \(\alpha\)-hydroxyketones and \(\alpha\)-diols are obtained through a regio- and stereocontrol of the reduction of acyclic \(\alpha\)-diketones by bakers' yeast. An investigation of the enzymatic system clearly demonstrates the role of two enzymes operating in sequence. An alcohol deh

Highly enantio- and diastereoselective r
✍ Tamotsu Fujisawa; Kengo Yamanaka; Bingidimi I. Mobele; Makoto Shimizu 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 175 KB

Bakers' yeast reduction of 2-phenylthiocyclopentanone, 2-phenylthiocyclohexanone, and 2phenylthio-2-cyclopentenone affords the corresponding (lS,2R)-2-phenylthiocycloalkanols in optically pure form and excellent diastereomeric excess. Cyclic P-phenylthiocycloalkanols possess potentially versatile pr