## Abstract The ^13^C NMR spectra of several monocyclic γ‐sultones(1,2‐oxathiolane 2,2‐dioxides) and δ‐sultones(1,2‐oxathiane 2,2‐dioxides) have been determined and are presented herein. The chemical shifts of the ring carbons of these compounds are compared in terms of conformational, electronic a
13C chemical shifts of Δ1-pyrrolines
✍ Scribed by Robert E. Gawley; Enrico J. Termine; Marta Goicoechea-Pappas
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 162 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C chemical shifts are reported for the ring carbons of several substituted Δ^1^‐pyrrolines. Average values for methine and methylene ring carbons facilitate structure elucidation of substituted δ^1^‐pyrrolines by ^13^C NMR spectroscopy.
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