DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kang, Taek | ko |
dc.contributor.author | Kim, Won-Yeob | ko |
dc.contributor.author | Yoon, Yeo-Kwon | ko |
dc.contributor.author | Kim, Byung-Gyu | ko |
dc.contributor.author | Lee, Hee-Yoon | ko |
dc.date.accessioned | 2013-03-11T06:16:18Z | - |
dc.date.available | 2013-03-11T06:16:18Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 2011-11 | - |
dc.identifier.citation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.133, no.45, pp.18050 - 18053 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | http://hdl.handle.net/10203/98487 | - |
dc.description.abstract | A tandem reaction strategy for forming triquinanes from linear allenyl diazo compounds through an intramolecular 1,3-dipolar cycloaddition reaction of an allenyl diazo group that generates a trimethylenemethane (TMM) diyl followed by an intramolecular [2 + 3] TMM diyl cycloaddition reaction has been developed. The new tandem cycloaddition reaction is readily applicable to the synthesis of complex molecules with high versatility and efficiency. | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | IDEAL SYNTHESIS | - |
dc.subject | CAPTURE | - |
dc.title | Tandem Cycloaddition Reactions of Allenyl Diazo Compounds Forming Triquinanes via Trimethylenemethane Diyls | - |
dc.type | Article | - |
dc.identifier.wosid | 000297381200013 | - |
dc.identifier.scopusid | 2-s2.0-80755136888 | - |
dc.type.rims | ART | - |
dc.citation.volume | 133 | - |
dc.citation.issue | 45 | - |
dc.citation.beginningpage | 18050 | - |
dc.citation.endingpage | 18053 | - |
dc.citation.publicationname | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.contributor.localauthor | Lee, Hee-Yoon | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | IDEAL SYNTHESIS | - |
dc.subject.keywordPlus | CAPTURE | - |
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