NMR experiments on acetals. 51. On the origin of the conformational behaviour of the trimethylammonium substituent: -N+Me3 substituted 1,3-dioxanes and -CH2N+Me3 substituted 1,3-dioxolanes and 1,3-dioxanes-Reference-Cited by-同舟云学术

NMR experiments on acetals. 51. On the origin of the conformational behaviour of the trimethylammonium substituent: -N+Me3 substituted 1,3-dioxanes and -CH2N+Me3 substituted 1,3-dioxolanes and 1,3-dioxanes

Published:2010-09-02 Issue:7-8 Volume:83 Page:285-294
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

van Cauwenberghe R.,Anteunis M.,Valckx L.

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19740830711/fullpdf

Reference18 articles.

1. NMR Experiments on Acetals. 40. Long Range Phenomena. 15. Some F, H long-range phenomena, configurational and conformational aspects from the 300 MHZ NMR spectra of 2-cf3-4-(chloro) methyl-1, 3-dioxolanes

2. R. van Anteunis Cauwenberghe , M. Chr. Becu J. Fluorine Chem

3. NMR experiments on acetals—XXXIX: Conformational insights through NMR studies at 300 MHz of 2-methyl-4-halogenomethyl-1,3-dioxolanes

4. Proton nuclear magnetic resonance spectra of 1-substituted acenaphthenes and other systems of well-defined geometry

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4. Conformational analysis of 5-membered ring compounds having cholinergic activity;Tetrahedron;1983-01