## Carbon -13 chemical shifts of l-phenylsulphonyl-2-phenylaziridine and several of its mand psubstituted derivatives have been determined. The substituent chemical shift (SCS) effects on the benzylic carbon C-2, and on the methylene carbon C-3 have been satisfactorily correlated with Hammett subs
Substituent effects on 13C and 1H chemical shifts in 3-benzylidene-2,4-pentanediones
✍ Scribed by E. Solčániova; P. Hrnčiar; T. Liptaj
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 275 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Substituent effects on the ^13^C and ^1^H chemical shifts have been studied for derivatives of 3‐benzylidene‐2, 4‐pentanedione. A significant correlation has been found between chemical shifts of the Z carbonyl group (C‐2) and Hammett constants, while no correlation has been found for the E carbonyl group (C‐4). Attempts have been made to determine the structural factors which influence these effects. The conformation of 3‐benzylidene‐2, 4‐pentanediones has been determined by ^13^C and ^1^H NMR spectroscopy.
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## 13 C and 1 H spectral assignments were made for three 2-substituted-and six 2,6-disubstituted naphthalenes with isopropyl, 2-hydroxy-2-methylethyl and 2-hydroperoxy-2-methylethyl substituents by the use of proton-proton decoupling, 2D H,H-COSY and 2D-C,H-COSY techniques. The downhill simplex me
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