ChemInform Abstract: Efficient 1,2-Asymmetric Induction in Radical Reactions: Addition of Acyl Radicals to 3-Hydroxy-1-(methylthio)-1-(p-tolylsulfonyl)-1-alkenes and Their Acetates.
β Scribed by Katsuyuki Ogura; Takayuki Arai; Akio Kayano; Motohiro Akazome
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Efficient 1,2-Asymmetric Induction in Radical Reactions: Addition of Acyl Radicals to 3-Hydroxy-1-(methylthio)-1-(p-tolylsulfonyl)-1alkenes and Their Acetates.
-Sensitized irradiation of aldehydes (II) generates acyl radicals which add to the functionalized alkenes (I). Desulfurization with Raney-Ni provides the products (IV) with high syn-selectivity. -
π SIMILAR VOLUMES
1999 hydroxycarboxylic acids hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters P 0280 ## 19 -084 Chelation-Controlled 1,3-Asymmetric Induction in Radical Addition to Ξ³-Hydroxy-and Ξ³-Alkoxy-Ξ±-methylenecarboxylic Esters. Ξ³-Oxy-Ξ±-methylenecarboxylic esters react with th
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