Free Radical-mediated Carboxylation by Radical Reactions of Alkyl Iodides with Methyl Oxalyl Chloride
Free radical-mediated carboxylation is achieved by treatment of alkyl iodides with methyl oxalyl chloride and bis(tributyltin) in benzene at 350 nm to afford the corresponding acid chlorides as a major product along with a small amount of the methyl esters. (C) 1998 Elsevier Science Ltd. All rights reserved.
- Publisher
- Pergamon-Elsevier Science Ltd
- Issue Date
- 1998-10
- Language
- English
- Article Type
- Article
- Keywords
ACYLATION APPROACH; SUBSTITUTION; KINETICS
- Citation
TETRAHEDRON LETTERS, v.39, no.40, pp.7317 - 7320
- ISSN
- 0040-4039
- Appears in Collection
- CH-Journal Papers(저널논문)
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