## Abstract Substrates (I) and (VI) react with chelation assistance of the quinoline N‐atom at the 8‐alkyl side chain to give monoacetoxylation products.
Chelation-assisted palladium-catalyzed acyloxylation of benzyl sp3 C–H bonds using PhI(OAc)2 as oxidant
✍ Scribed by Shouhui Zhang; Fang Luo; Wenhui Wang; Xiaofei Jia; Maolin Hu; Jiang Cheng
- Book ID
- 104097755
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 566 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A chelation-assisted palladium-catalyzed acyloxylation of the sp 3 C-H bond of benzyl by carboxylic acid is described, which employs PhI(OAc) 2 as a stoichiometric oxidant. The procedure tolerates a series of functional groups, such as methoxyl, chloro, bromo, iodo, vinyl, formyl, phenolic hydroxyl, nitro, and cyano groups, providing the acyloxylation products in moderate to good yields.
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