Aureobasidium pullulans as a key for the preparation of optical purity (R)-2-(anthracen-9-yl)-2-methoxyacetic acid – The chiral auxiliary reagent in determination of absolute configuration
- 1 November 2015
- journal article
- Published by Elsevier in Journal of Molecular Catalysis B: Enzymatic
- Vol. 121, 28-31
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Asymmetric reduction of (4R)-(−)-carvone catalyzed by Baker's yeast in aqueous mono- and biphasic systemsJournal of Molecular Catalysis B: Enzymatic, 2012
- Chiral resolutions of (9‐anthryl)methoxyacetic acid and (9‐anthryl)hydroxyacetic acid by capillary electrophoresisChirality, 2007
- Determining the Absolute Stereochemistry of Secondary/Secondary Diols by 1H NMR: Basis and ApplicationsThe Journal of Organic Chemistry, 2005
- The Assignment of Absolute Configuration by NMRChemical Reviews, 2004
- Simultaneous enantioresolution and assignment of absolute configuration of secondary alcohols by directly coupled HPLC–NMR of 9-AMA estersTetrahedron: Asymmetry, 2002
- Baker's yeast mediated reduction of β-keto esters and β-keto amides in an organic solvent systemJournal of Molecular Catalysis B: Enzymatic, 2001
- 9-Anthrylmethoxyacetic acid esterification shifts—Correlation with the absolute stereochemistry of secondary alcoholsTetrahedron, 1999
- Biotransformation of monoterpenoid ketones by yeasts and yeast-like fungiJournal of Molecular Catalysis B: Enzymatic, 1998
- Determination of the absolute configuration of alcohols by low temperature 1H NMR of aryl(methoxy)acetatesTetrahedron: Asymmetry, 1995
- Effect of Allyl Alcohol on Reduction of β-Keto Esters by Bakers’ YeastChemistry Letters, 1987