✦ LIBER ✦

ChemInform Abstract: Chemoenzymatic Deracemization of (.+-.)-2,2-Disubstituted Oxiranes.

✍ Scribed by R. V. A. ORRU; S. F. MAYER; W. KROUTIL; K. FABER

Publisher: John Wiley and Sons
Year: 2010
Weight: 40 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199821040

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Chemoenzymatic Dera

ChemInform Abstract: Chemoenzymatic Deracemization Methods

✍ Davide Tessaro; Gianluca Molla; Loredano Pollegioni; Stefano Servi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 11 KB

ChemInform Abstract: Synthesis of Enanti

ChemInform Abstract: Synthesis of Enantiomerically Pure 2,3-Disubstituted Oxirane-2-carboxamides.

✍ J. L. GARCIA RUANO; A. M. MARTIN CASTRO; J. H. RODRIGUEZ RAMOS; A. C. RUBIO FLAM 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

ChemInform Abstract: Deracemization of (

ChemInform Abstract: Deracemization of (.+-.)-2,2-Disubstituted Epoxides via Enantioconvergent Chemoenzymatic Hydrolysis Using Nocardia EH1 Epoxide Hydrolase and Sulfuric Acid.

✍ R. V. A. ORRU; W. KROUTIL; K. FABER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

ChemInform Abstract: Stereocontrolled Ch

ChemInform Abstract: Stereocontrolled Chemoenzymatic Synthesis of 2,3-Disubstituted Piperidines.

✍ Maria I. Monterde; Rosario Brieva; Vicente Gotor 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: Deracemization of (

ChemInform Abstract: Deracemization of (.+-.)-2,3-Disubstituted Oxiranes via Biocatalytic Hydrolysis Using Bacterial Epoxide Hydrolases: Kinetics of an Enantioconvergent Process.

✍ W. KROUTIL; M. MISCHITZ; K. FABER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Chemoenzymatic Synthesis of (2S)- and (2

Chemoenzymatic Synthesis of (2S)- and (2R)-2-(1,3-Dithian-2-ylmethyl)oxirane

✍ Eirik Sundby; Jarle Holt; Anders Vik; Thorleif Anthonsen 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 106 KB

## Abstract Lipase‐catalyzed transesterifications and biological reductions were used to obtain the (__S__)‐enantiomers of 3‐chloro‐1‐(1,3‐dithian‐2‐yl)‐2‐propanol and 1‐(1,3‐dithian‐2‐yl)‐3‐fluoro‐2‐propanol and their (__R__)‐acetates. (__S__)‐3‐Chloro‐1‐(1,3‐dithian‐2‐yl)‐2‐propanol and (__R__)‐3