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ChemInform Abstract: Reductive Opening of Cyclopropylogous α-Hydroxy Aldehydes and Ketones by Samarium(II) Iodide.
✍ Scribed by A. NIVLET; V. LE GUEN; L. DECHOUX; T. LE GALL; C. MIOSKOWSKI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Reductive Opening of Cyclopropylogous α-Hydroxy Aldehydes and Ketones by Samarium(II) Iodide.
-The regioselectivity of the title reaction is found to be strongly dependant on the substitution pattern of the substrate. In several cases, a tandem cyclopropyl opening-deoxygenation reaction leads to γ-carbonyl alkenes.
-(NIVLET, A.
📜 SIMILAR VOLUMES
Hydrodimerization of Cyclic α,β Unsaturated Ketones Promoted by Samarium Iodide. -The intermolecular coupling of cyclic unsaturated ketones by SmI 2 /THF and SmI 2 /HMPA/THF systems, resp., affords symmetrical hydrodimers in a short reaction time and in good yields. The use of HMPA improves the yie