The influence of sulfur configuration in 1 H NMR chemical shifts of diasteromeric five-membered cyclic sulfites

The effect of the stereochemistry of the sulfur atom on H chemical shifts of the diasteromeric pair of cyclic sulfites of 4-[methoxy(4-nitrophenyl)methyl]-5-phenyl-1,3,2-dioxathiolan-2-oxide was investigated. The complete H and C NMR spectral assignment was achieved by the use of one-dimensional and...

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Bibliographic Details

Published in:	Magnetic resonance in chemistry Vol. 55; no. 3; pp. 233 - 238
Main Authors:	Obregón-Mendoza, Marco A, Sánchez-Castellanos, Mariano, Cuevas, Gabriel, Gnecco, Dino, Cassani, Julia, Poveda-Jaramillo, Juan C, Reynolds, William F, Enríquez, Raúl G
Format:	Journal Article
Language:	English
Published:	England 01-03-2017
Subjects:	electron delocalization index NMR characterization cyclic sulfites 1,3,2-dioxathiolan-2-oxides
Online Access:	Get full text
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