Free Radical-mediated Carboxylation by Radical Reactions of Alkyl Iodides with Methyl Oxalyl Chloride
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Sung Gak | ko |
| dc.contributor.author | s. y. jon | ko |
| dc.date.accessioned | 2013-02-28T03:24:59Z | - |
| dc.date.available | 2013-02-28T03:24:59Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1998-10 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.39, no.40, pp.7317 - 7320 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/72528 | - |
| dc.description.abstract | 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. | - |
| dc.language | English | - |
| dc.publisher | Pergamon-Elsevier Science Ltd | - |
| dc.subject | ACYLATION APPROACH | - |
| dc.subject | SUBSTITUTION | - |
| dc.subject | KINETICS | - |
| dc.title | Free Radical-mediated Carboxylation by Radical Reactions of Alkyl Iodides with Methyl Oxalyl Chloride | - |
| dc.type | Article | - |
| dc.identifier.wosid | 000075884200031 | - |
| dc.identifier.scopusid | 2-s2.0-0032190831 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 39 | - |
| dc.citation.issue | 40 | - |
| dc.citation.beginningpage | 7317 | - |
| dc.citation.endingpage | 7320 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.contributor.localauthor | Kim, Sung Gak | - |
| dc.contributor.nonIdAuthor | s. y. jon | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | ACYLATION APPROACH | - |
| dc.subject.keywordPlus | SUBSTITUTION | - |
| dc.subject.keywordPlus | KINETICS | - |
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