✦ LIBER ✦

Enantioselective CC bond reduction of unsaturated α-chloro esters by old yellow enzymes

✍ Scribed by Elisabetta Brenna; Giovanni Fronza; Claudio Fuganti; Daniela Monti; Fabio Parmeggiani

Book ID: 113804895
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 415 KB
Volume: 73
Category: Article
ISSN: 1381-1177
DOI: 10.1016/j.molcatb.2011.07.008

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Unusual CC Bond Isomerization of an α,β

Unusual CC Bond Isomerization of an α,β-Unsaturated γ-Butyrolactone Catalysed by Flavoproteins from the Old Yellow Enzyme Family

✍ Durchschein, Katharina; Wallner, Silvia; Macheroux, Peter; Zangger, Klaus; Fabia 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 403 KB

Enantioselective Reductive Coupling of 1

Enantioselective Reductive Coupling of 1,3-Enynes to Glyoxalates Mediated by Hydrogen: Asymmetric Synthesis of β,γ-Unsaturated α-Hydroxy Esters

✍ Hong, Young-Taek; Cho, Chang-Woo; Skucas, Eduardas; Krische, Michael J. 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 140 KB

Steric Effects on the Stereochemistry of

Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural Modifications

✍ Brenna, Elisabetta; Gatti, Francesco G.; Manfredi, Alessia; Monti, Daniela; Parm 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 353 KB

ChemInform Abstract: Enantioselective Re

ChemInform Abstract: Enantioselective Reductive Coupling of 1,3-Enynes to Glyoxalates Mediated by Hydrogen: Asymmetric Synthesis of β,γ-Unsaturated α-Hydroxy Esters.

✍ Young-Taek Hong; Chang-Woo Cho; Eduardas Skucas; Michael J. Krische 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Biotransformation o

ChemInform Abstract: Biotransformation of α,β-Unsaturated Carbonyl Compounds: Sulfides, Sulfoxides, Sulfones, Nitriles, and Esters by Yeast Species: Carbonyl Group and Carbon-Carbon Double Bond Reduction.

✍ S. KOUL; D. H. G. CROUT; W. ERRINGTON; J. TAX 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB