## Abstract From a 300 MHz spectral study of monoβto trisubstituted cyclohexanes, allowing a reβexamination of some of their ^1^H NMR spectral parameters, it is shown that it is possible to predict with reasonable accuracy the shifts (in CCl~4~) of the ring protons. A substantial feature in this is
β¦ LIBER β¦
1H-NMR study on acylamino acids. Relationship between the chemical shift of amide protons and electronegativity of acyl groups
β Scribed by Yasuyuki Shimohigashi; Tetsuo Kato; Shinwon Kang; Yoshihiro Minematsu; Michinori Waki; Nobuo Izumiya
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 121 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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