Numerous areneselenenamides derived from ammonia, primary and secondary amines and two N,N-bis(ary1-se1eno)alkylamines have been studied. The selenenamides bearing an electron-withdrawing substituent on the aromatic moiety are stable. The 'H, 13C and 77Se chemical shifts and some coupling constants
77Se, 13C and 1H NMR spectra of phenylselenenyl azide and chloride addition products of methylenecyclohexane and cyclohexene
✍ Scribed by Walter J. Boyko; Franco J. Duarte; Robert M. Giuliano
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 298 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^77^Se, ^13^C and ^1^H NMR spectra of the products of phenylselenenyl azide and chloride addition to methylenecyclohexane and cyclohexene are presented. Scalar couplings between ^77^Se and ^1^H/^13^C allowed the absolute assignment of the regioisomers in the ^1^H and ^13^C spectra. Low‐temperature ^77^Se NMR was used to determine the conformer ratios for 1‐azidomethyl‐ and 1‐chloromethyl‐1‐phenylselenenylcyclohexane anti‐Markovnikov addition products.
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