## Abstract ^77^Se and ^13^C chemical shift of 19 1,2,3‐selenadiazoles are discussed in terms of substituent effects and conforma‐tional behaviour of the molecules. It is shown that the ^77^Se chemical shifts of such compounds are suitable tools for chiral discrimination in diastereomeric compounds
77Se and 15N NMR investigation of some cycloalkeno-1,2,3-selenadiazole derivatives
✍ Scribed by Helmut Duddeck; Petra Wagner; Dieter Müller; Joseph Csaba Jászberényi
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 390 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C, ^15^N and ^77^Se NMR data (chemical shifts and coupling constants) of some cycloakeno‐1,2,3‐selenadiazoles are presented. Extremely large ^77^Se chemical shifts are found. ^15^N, ^77^Se coupling constants, obtained at natural abundance, are reported for the first time. Strong signal shifts due to different sizes of the cycloakeno rings can be qualitatively rationalized in terms of electron transfer between the nitrogen and selenium atoms. A positive γ‐syn effect of the methyl group on N‐3 is found in 4‐methyl‐4,5,6,7‐tetrahydrobenzo‐1,2,3‐selenadiazole.
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