Novel cyclization mediated by organocopper reagents
β Scribed by Katzenellenbogen, John A.; Corey, E. J.
- Book ID
- 127274010
- Publisher
- American Chemical Society
- Year
- 1972
- Tongue
- English
- Weight
- 292 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
Asymmetric arene-alkene cyclization reactions mediated by a chiral electrophilic organoselenium reagent afforded substituted carbocyclic derivatives with high diastereoselectivities. It was also found that [3-methoxyselenides are good precursors of seleniranium ions when treated with strong acids.
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The iodine-magnesium exchange reaction with i-PrMgCl allows a mild preparation of functionalized arylmagnesium compounds bearing a leaving group in the molecule. With the appropriate transition-metal catalyst (a copper or cobalt salt), cyclization reactions occur leading to five-or six-membered ring