DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Hee Yoon | ko |
dc.contributor.author | Song, Seog-Beom | ko |
dc.contributor.author | Kang, Taek | ko |
dc.contributor.author | Kim, Yoon Jung | ko |
dc.contributor.author | Geum, Su Jeong | ko |
dc.date.accessioned | 2013-06-07T08:08:20Z | - |
dc.date.available | 2013-06-07T08:08:20Z | - |
dc.date.created | 2013-05-07 | - |
dc.date.created | 2013-05-07 | - |
dc.date.issued | 2013-03 | - |
dc.identifier.citation | PURE AND APPLIED CHEMISTRY, v.85, no.4, pp.741 - 753 | - |
dc.identifier.issn | 0033-4545 | - |
dc.identifier.uri | http://hdl.handle.net/10203/173858 | - |
dc.description.abstract | Aziridinyl imines are well-known carbene equivalents because they are precursors of diazo compounds from which reactive intermediates can be produced. These carbene equivalents can be utilized as zwitterionic species, diradicals, or 4 pi system for cycloaddition reactions. Thus, the intermediates derived from aziridinyl imines have been used in the sulfur-ylide-mediated epoxide formation, tandem free-radical reactions, or cyclopropanation reaction via carbene intermediates to form trimethylenemethane (TMM) diyls, which undergo [2 + 3] cycloaddition reactions to form cyclopentanoids. Diazo compounds generated from aziridinyl imines also react with allenes to form TMM diyls. This reaction was utilized in tandem cycloaddition reactions of linear substrates to form polyquinanes. These tandem reaction strategies were successfully applied to the total synthesis of various cyclopentanoid natural products. | - |
dc.language | English | - |
dc.publisher | INT UNION PURE APPLIED CHEMISTRY | - |
dc.subject | TRIMETHYLENEMETHANE DIYLS | - |
dc.subject | CYCLOADDITION REACTIONS | - |
dc.subject | ALKYLIDENE CARBENES | - |
dc.subject | DIAZO-COMPOUNDS | - |
dc.subject | GENERATION | - |
dc.subject | ALPHA | - |
dc.subject | TRIQUINANES | - |
dc.subject | REARRANGEMENT | - |
dc.subject | BIOSYNTHESIS | - |
dc.subject | CYCLIZATION | - |
dc.title | Aziridinyl imines in organic synthesis: Development of tandem reaction strategies and application to total synthesis of natural products | - |
dc.type | Article | - |
dc.identifier.wosid | 000316740300009 | - |
dc.identifier.scopusid | 2-s2.0-84875760316 | - |
dc.type.rims | ART | - |
dc.citation.volume | 85 | - |
dc.citation.issue | 4 | - |
dc.citation.beginningpage | 741 | - |
dc.citation.endingpage | 753 | - |
dc.citation.publicationname | PURE AND APPLIED CHEMISTRY | - |
dc.identifier.doi | 10.1351/PAC-CON-12-10-01 | - |
dc.contributor.localauthor | Lee, Hee Yoon | - |
dc.contributor.nonIdAuthor | Song, Seog-Beom | - |
dc.contributor.nonIdAuthor | Kang, Taek | - |
dc.contributor.nonIdAuthor | Kim, Yoon Jung | - |
dc.contributor.nonIdAuthor | Geum, Su Jeong | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | cycloadditions | - |
dc.subject.keywordAuthor | domino reactions | - |
dc.subject.keywordAuthor | hydrazones | - |
dc.subject.keywordAuthor | polycyclic compounds | - |
dc.subject.keywordAuthor | radical reactions | - |
dc.subject.keywordAuthor | tandem reactions | - |
dc.subject.keywordAuthor | total synthesis | - |
dc.subject.keywordAuthor | trimethylenemethane | - |
dc.subject.keywordPlus | TRIMETHYLENEMETHANE DIYLS | - |
dc.subject.keywordPlus | CYCLOADDITION REACTIONS | - |
dc.subject.keywordPlus | ALKYLIDENE CARBENES | - |
dc.subject.keywordPlus | DIAZO-COMPOUNDS | - |
dc.subject.keywordPlus | GENERATION | - |
dc.subject.keywordPlus | ALPHA | - |
dc.subject.keywordPlus | TRIQUINANES | - |
dc.subject.keywordPlus | REARRANGEMENT | - |
dc.subject.keywordPlus | BIOSYNTHESIS | - |
dc.subject.keywordPlus | CYCLIZATION | - |
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