α-Methoxyphenyl acetic acid (MPA) for the configurational assignment of aromatic–heteroaromatic carbinols by 1H NMR spectroscopy
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Highly Enantioselective Hydrogenation of Aromatic-Heteroaromatic Ketones
2. A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR
3. The Assignment of Absolute Configuration by NMR
4. A Very Reliable Method for Determination of Absolute Configuration of Chiral Secondary Alcohols by 1H NMR Spectroscopy
5. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
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1. Enantioselective Reduction of Diaryl Ketones Catalyzed by a Carbonyl Reductase fromSporobolomyces salmonicolorand its Mutant Enzymes;Advanced Synthesis & Catalysis;2009-03
2. Preparation of pyridinyl aryl methanol derivatives by enantioselective hydrogenation of ketones using chiral Ru(diphosphine)(diamine) complexes. Attribution of their absolute configuration by 1H NMR spectroscopy using Mosher's reagent;Tetrahedron;2008-09
3. Preparation of single-enantiomer 2-methyl-4-heptanol, a pheromone of Metamasius hemipterus, using (S)-2-methoxy-2-(1-naphthyl)propionic acid;Journal of Chromatography A;2006-06
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