Free radical additions to benzonorbornadiene
β Scribed by Leon E. Barstow; George A. Wiley
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 142 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
SVALSNE Is cycllsed to a number of other triterpenes, lncludlnq the Precursor of lanosterol and thus of chplesterol, by orldatlve hydroxylatlon of a terminal double bond? It Is usually suggested that this 13 a two-electron Process, involving "OX+", but it has seemed
Attack of a free-radical on norbornene or norbornadiene is generally thought to occur from the 8x0 side (1,2), although exceptions have been reported (3). There are many examples of exo-addition to norbornene by freeradicals (11, but few studies have been made on the sterochemistry of freeradical ad
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