1H and 13C NMR spectral and X-ray crystallographic study of 3-methyl-2,4-diphenylquinoline. Sterically hindered phenyl groups and the ‘pseudo peri-proximity’ effect-Reference-Cited by-同舟云学术

1H and 13C NMR spectral and X-ray crystallographic study of 3-methyl-2,4-diphenylquinoline. Sterically hindered phenyl groups and the ‘pseudo peri-proximity’ effect

Published:1995-02 Issue:2 Volume:51 Page:237-246
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Osborne Alan G.,Ahmet Mustafa T.,Miller John R.,Warmsley Joanne F.

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference18 articles.

1. 1H and 13C NMR spectral studies of some 2,4-diphenylquinoline derivatives

2. 13C NMR spectral studies of some methoxycoumarin derivatives. A re-assignment for citropten (limettin) and an examination ofPeri-proximity effects for the methyl-methoxy and methoxy-methyl couples

3. Lewis Acid-Catalyzed Cyclization of 3-Amino-2-alkenimines. Synthesis of Quinolines

4. Single-Frequency Proton Decoupling in 13C N.M.R. Spectra. 13C Chemical Shifts and Methyl Substituent Chemical Shifts in Methylquinolines

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