DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Sung Gak | ko |
dc.contributor.author | Lee, TA | ko |
dc.contributor.author | Song, Y | ko |
dc.date.accessioned | 2013-02-28T00:21:13Z | - |
dc.date.available | 2013-02-28T00:21:13Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1998-05 | - |
dc.identifier.citation | SYNLETT, no.5, pp.471 - 471 | - |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.uri | http://hdl.handle.net/10203/71715 | - |
dc.description.abstract | N-Alkoxyphthalimides, stable and readily accessible from alcohols and alkyl halides, are found to be very efficient alkoxy radical precursors. | - |
dc.language | English | - |
dc.publisher | GEORG THIEME VERLAG | - |
dc.subject | PHOTOINDUCED MOLECULAR-TRANSFORMATIONS | - |
dc.subject | CENTERED RADICALS | - |
dc.subject | ORGANIC-SYNTHESIS | - |
dc.subject | TRIS(TRIMETHYLSILYL)SILANE | - |
dc.subject | KETONES | - |
dc.title | Facile generation of alkoxy radicals from N-alkoxyphthalimides | - |
dc.type | Article | - |
dc.identifier.wosid | 000074207500005 | - |
dc.type.rims | ART | - |
dc.citation.issue | 5 | - |
dc.citation.beginningpage | 471 | - |
dc.citation.endingpage | 471 | - |
dc.citation.publicationname | SYNLETT | - |
dc.contributor.localauthor | Kim, Sung Gak | - |
dc.contributor.nonIdAuthor | Lee, TA | - |
dc.contributor.nonIdAuthor | Song, Y | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | alkyl halides | - |
dc.subject.keywordAuthor | alcohols | - |
dc.subject.keywordAuthor | N-alkoxyphthalimides | - |
dc.subject.keywordAuthor | alkoxy radical precursors | - |
dc.subject.keywordPlus | PHOTOINDUCED MOLECULAR-TRANSFORMATIONS | - |
dc.subject.keywordPlus | CENTERED RADICALS | - |
dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
dc.subject.keywordPlus | TRIS(TRIMETHYLSILYL)SILANE | - |
dc.subject.keywordPlus | KETONES | - |
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