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ChemInform Abstract: Imidyl Radicals. Part 3. Stereoselectivity of Radical Additions of N-Haloimides to Cyclic Alkenes.

✍ Scribed by Andre Kirsch; Ulrich Luening; Oliver Krueger

Publisher
John Wiley and Sons
Year
2010
Weight
37 KB
Volume
31
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES

Imidyl radicals. 3. Stereoselectivity of
Imidyl radicals. 3. Stereoselectivity of radical additions of N-haloimides to cyclic alkenes
✍ AndrΓ© Kirsch; Ulrich LΓΌning; Oliver KrΓΌger πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 66 KB πŸ‘ 1 views

N-Haloimides (1 -5) are used in two types of radical chain reactions: (i) the selective Ziegler bromination of allylic and benzylic positions [1], which are bromine atom chain reactions [2] and (ii) imidyl radical [3, 4] chain reactions like substitutions and especially additions to double bonds [5,

ChemInform Abstract: Free Radical Additi
ChemInform Abstract: Free Radical Addition of Ξ±-Telluroesters to Alkenes.
✍ Nobuaki Kambe; Li-Biao Han; Shin-ichi Fujiwara; Noboru Sonoda πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 36 KB

## Abstract The title reaction leads to the compounds (III), (VI), (VIII), and (X) and suppresses the competing olefin polymerization.