Free radical-mediated acylation and carboxylation reactions

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Radical acylations to prepare carbonyl compounds are described and focus on indirect acylation approaches using sulfonyl oxime ethers under tin-mediated and tin-free conditions. The efficiency of carboxylic acid derivatives as carbonyl group radical acceptors in radical acylation and carboxylation reactions is discussed.
Publisher
Wiley-Blackwell
Issue Date
2004-01
Language
English
Article Type
Review
Keywords

PHENYLSULFONYL OXIME ETHERS; ALKENE ADDITION-REACTIONS; INTRAMOLECULAR CYCLIZATION REACTIONS; GROUP-TRANSFER IMIDOYLATION; ALKYL ALLYL SULFONES; CARBON-CARBON BONDS; ACYL RADICALS; ORGANOTELLURIUM COMPOUNDS; REAGENT EQUIVALENTS; CHAIN-REACTIONS

Citation

ADVANCED SYNTHESIS & CATALYSIS, v.346, no.1, pp.19 - 32

ISSN
1615-4150
DOI
10.1002/adsc.200303128
URI
http://hdl.handle.net/10203/80587
Appears in Collection
CH-Journal Papers(저널논문)
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