Determination of the absolute configuration of chiral secondary alcohols; new advances using 13C- and 2D-NMR spectroscopy
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference18 articles.
1. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
2. Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives
3. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
4. On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols
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2. REFERENCES;Differentiation of Chiral Compounds Using NMR Spectroscopy;2018-06-15
3. Lipase-catalyzed stereoresolution of long-chain 1,2-alkanediols: A screening of preferable reaction conditions;Journal of Molecular Catalysis B: Enzymatic;2015-06
4. A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides;Advances in Chemistry;2014-08-10
5. An Assessment of Alternative Low Level Calculation Methods for the Initial Selection of Conformers of Diastereomeric Esters;Journal of Theoretical Chemistry;2014-06-23
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