Etudes par la RMN du carbone-13 de quelques dérivés cyclopropaniques: Déplacements chimiques et paramètres structuraux
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry,General Materials Science,General Chemistry
Reference35 articles.
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2. Theoretical and empirical calculations of the carbon chemical shift in terms of the electronic distribution in molecules
3. Substituent Effects. VI. Theoretical Interpretation of Additivity Rules of NMR Using McWeeny Group Functions
4. Carbon-13 magnetic resonance. XXI. Steric interactions in the methylcyclohexanes
5. Substituent Effects. V.1 Correlation of C13 Chemical Shifts by Pairwise Interactions
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1. Carbon-13 NMR of fluorocyclopropanes;Magnetic Resonance in Chemistry;2008
2. Substituent Effects on13C Chemical Shifts in Aliphatic Molecular Systems. Dependence on Constitution and Stereochemistry;Topics in Stereochemistry;2007-02-26
3. Electrophilic Intermediates and Their Reactions in Superacids;The Journal of Organic Chemistry;2006-05-01
4. Diastereoselective synthesis of trans-1,2-disubstituted cyclopropanols from homoallyl or bis-homoallyl esters via tandem intramolecular nucleophilic acyl substitution and intramolecular carbonyl addition reactions mediated by Ti(OPr-i)4 / 2 i-PrMgBr reagent;Tetrahedron Letters;1995-08
5. Stable carbocations. 285. 1-Ferrocenyl-1-cyclopropyl cation: the first long-lived cyclopropyl cation;Journal of the American Chemical Society;1992-01
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