Thieme Chemistry Journal Awardees - Where Are They Now? Diastereoselective Tandem Iodocarbonate Cyclization of 1,5-Enynes
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lim, Choongmin | - |
dc.contributor.author | Rao, M. Shesha | - |
dc.contributor.author | Shin, Seunghoon | - |
dc.date.accessioned | 2022-12-20T19:02:37Z | - |
dc.date.available | 2022-12-20T19:02:37Z | - |
dc.date.created | 2022-08-27 | - |
dc.date.issued | 2010-02 | - |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/175473 | - |
dc.description.abstract | A diastereoselective, metal-free tandem iodocarbonate-cyclization of 1,5-enyne, emulating the reactivity of gold catalysis is described. The normal selectivity of iodonium reagents for alkene is reversed favoring alkyne activation in the presence of aryl alkynes. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | GEORG THIEME VERLAG KG | - |
dc.title | Thieme Chemistry Journal Awardees - Where Are They Now? Diastereoselective Tandem Iodocarbonate Cyclization of 1,5-Enynes | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Shin, Seunghoon | - |
dc.identifier.doi | 10.1055/s-0029-1219183 | - |
dc.identifier.scopusid | 2-s2.0-76349111564 | - |
dc.identifier.wosid | 000274233900003 | - |
dc.identifier.bibliographicCitation | SYNLETT, no.3, pp.368 - 373 | - |
dc.relation.isPartOf | SYNLETT | - |
dc.citation.title | SYNLETT | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 368 | - |
dc.citation.endPage | 373 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | CATALYZED CASCADE REACTIONS | - |
dc.subject.keywordPlus | TERT-BUTYL CARBONATES | - |
dc.subject.keywordPlus | GOLD(I)-CATALYZED FORMATION | - |
dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
dc.subject.keywordPlus | DOMINO REACTIONS | - |
dc.subject.keywordPlus | GOLD | - |
dc.subject.keywordPlus | CYCLOISOMERIZATION | - |
dc.subject.keywordPlus | ENYNES | - |
dc.subject.keywordPlus | IONS | - |
dc.subject.keywordPlus | N&apos | - |
dc.subject.keywordPlus | -(2-ALKYNYLBENZYLIDENE)HYDRAZIDES | - |
dc.subject.keywordAuthor | enynes | - |
dc.subject.keywordAuthor | iodocyclization | - |
dc.subject.keywordAuthor | IBr | - |
dc.subject.keywordAuthor | tandem reactions | - |
dc.subject.keywordAuthor | diastereoselectivity | - |
dc.identifier.url | https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0029-1219183 | - |
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