Abstract
The complete carbon-13 nmr spectra of 16 alkylated 2,5-dihydrothiophenes and 10 sulfones derived from them are reported. No significant interactions between C-2 substituents and C-5 are noted and stereochemical determinations based on this γ effect are not possible. On oxidation to the sulfones, C-2 and C-5 are dramatically deshielded but C-3 and C-4 are shielded. A possible explanation for this effect is presented.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
11 articles.
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