## Abstract Vicinal ^13^C, ^1^H coupling constants were used to establish the configuration of a 3,5βdisubstituted notricyclene. The assignment procedure is supported by independent measurements of ^13^C, ^2^H coupling constants in 3β deuterionortricyclene and confirmed by ^1^H, ^1^H NOE data for _
Vicinal 13CH coupling through olefinic double bonds
β Scribed by Alan W. Douglas
- Book ID
- 102525367
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 204 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
Values of long range ^13^CH coupling through the double bond in a number of isopropenyl compounds are reported. There is evidence that substituent dependence of ^3^J(CH) is not related linearly to that of Hο£ΏH couplings in vinyl compounds. The ratio of ^3^J(CH) to ^3^J(HH) in analogous pairs of compounds appears to increase with decreasing substituent polarity and increasing steric bulk.
π SIMILAR VOLUMES
Scheme 1
## Abstract The design and development of highly efficient and selective methods for the synthesis of Οβconjugated arylvinyl derivatives, based on sequential catalytic reactions of organometallic reagents, have been the subject of extensive study because of their versatile application in organic sy
In vicinally-disubstituted olefins, the magnitude of the hydrogen-hydrogen coupling