✦ LIBER ✦

Bacterial epoxide hydrolases of opposite enantiopreference

✍ Scribed by Wolfram Krenn; Ingrid Osprian; Wolfgang Kroutil; Gerhart Braunegg; Kurt Faber

Book ID: 110225910
Publisher: Springer Netherlands
Year: 1999
Tongue: English
Weight: 42 KB
Volume: 21
Category: Article
ISSN: 0141-5492
DOI: 10.1023/a:1005565108510

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Modification of Substrate Specificity Re

Modification of Substrate Specificity Resulting in an Epoxide Hydrolase with Shifted Enantiopreference for (2,3-Epoxypropyl)benzene

✍ Ann Gurell; Mikael Widersten 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 410 KB

ChemInform Abstract: Chemoenzymatic Synt

ChemInform Abstract: Chemoenzymatic Synthesis of (S)-(-)-Frontalin Using Bacterial Epoxide Hydrolases.

✍ W. KROUTIL; I. OSPRIAN; M. MISCHITZ; K. FABER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Chemoenzymatic Synthesis of (S)-(-)-Frontalin Using Bacterial Epoxide Hydrolases. -The title compound (III) is an aggregation pheromone of pine beetles.

Enantioselective Hydrolysis of Functiona

Enantioselective Hydrolysis of Functionalized 2,2-Disubstituted Oxiranes with Bacterial Epoxide Hydrolases

✍ Andreas Steinreiber; Ingrid Osprian; Sandra F. Mayer; Romano V. A. Orru; Kurt Fa 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 295 KB

Synthetic applications of epoxide hydrol

Synthetic applications of epoxide hydrolases

✍ Alain Archelas; Roland Furstoss 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 93 KB

Stereoselectivities of microbial epoxide

Stereoselectivities of microbial epoxide hydrolases

✍ Romano VA Orru; Kurt Faber 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 102 KB

Epoxide hydrolases from bacterial and fungal sources are highly versatile biocatalysts for the asymmetric hydrolysis of epoxides on a preparative scale. Besides kinetic resolution, which yields the corresponding enantiomerically enriched vicinal diol and the remaining nonconverted epoxide, enantioco

Biocatalytic resolution of 2-methyl-2-(a

Biocatalytic resolution of 2-methyl-2-(aryl)alkyloxiranes using novel bacterial epoxide hydrolases

✍ I. Osprian; W. Kroutil; M. Mischitz; K. Faber 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 420 KB

Biocatalytic resolution of alkyl-and (arylalkyl)-oxiranes was accomplished by employing the epoxide hydrolase activity of lyophilized whole cells of seven bacterial strains belonging to the genera Rhodococcus, Mycobacterium and Nocardia. Whereas no suitable biocatalyst was found for 1-octene oxide,