Differentiation of diastereomeric 2-substituted cyclohexanamines with three chirality centres by13C NMR spectroscopy
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry
Reference15 articles.
1. Carbon-13 NMR Spectroscopy, p. 71. Academic Press, New York (1972).
2. The differentiation of diastereomers by13C NMR spectroscopy
3. 13C RMN: Non-équivalences d'ammoniums quaternaires diastéréoisoméres
4. 13C NMR Spectroscopy of Substituted Cyclohexanes
5. Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy
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1. Determination of the conformations and relative configurations of exocyclic amines;Magnetic Resonance in Chemistry;2010-10-28
2. Reliable 13C NMR Method of Making Relative Stereochemical Assignments to Certain N-[α-Hetero-β-hydroxy(acetoxy)-β-(substituted phenyl)-1‘-oxopropyl]-2-oxazolidinones;The Journal of Organic Chemistry;1997-01-01
3. New investigations of the reaction of epichlorohydrin with hindered amines: X-ray and NMR analyses;Canadian Journal of Chemistry;1989-10-01
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