## Abstract The ^13^C NMR chemical shifts for 1,3‐dithiolane and 13 methyl substituted derivatives are reported. Substituent effects are derived and compared with those for cyclopentanes and 1,3‐dioxolanes. The magnitude and variety of the substituent effects are best explained with the aid of a ha
13C NMR studies of heterocyclic naphtho- and anthraquinones. Deshielding effect on the carbonyl carbon with methyl substitution
✍ Scribed by Cristian Salas; Veronica Armstrong; Claudio López; Ricardo A. Tapia
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 123 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2156
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✦ Synopsis
Abstract
^13^C chemical shift assignment of several methyl substituted heterocyclic naphtho‐ and anthraquinones, including dihydronaphthofuranquinones, azaanthraquinones, benzopyrroloquinolinediones and benzothiophenoquinolinediones, are described. A deshielding effect due to a methyl group was observed over the neighbouring carbonyl carbon, in every case studied. ^13^C assignments were based on 2D experiments. Copyright © 2007 John Wiley & Sons, Ltd.
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