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dc.contributor.authorKim, Sang Hee-
dc.contributor.authorKim, Hyung Gyu-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorCha, Joo Hwan-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorKoh, Hun Yeong-
dc.contributor.authorChung, Bong Young-
dc.contributor.authorCho, Yong Seo-
dc.date.accessioned2024-01-21T02:31:24Z-
dc.date.available2024-01-21T02:31:24Z-
dc.date.created2021-09-01-
dc.date.issued2006-09-04-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/135134-
dc.description.abstractN-Acyliminium ion cyclizations were studied with allenylmethylsilanes to synthesize nitrogen heterocycles. N-Acyliminium ion cyclizations were carried out by exposure of precursors 6 and 7 to Lewis acid. The precursors 6 were converted to pyrrolizidinone derivatives 9 with an exo-allene moiety, while the precursors 7 to indolizidinone derivatives 10 with an exo-1,3-diene moiety. (c) 2006 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCHEMISTRY-
dc.titleN-Acyliminium ion cyclizations of trimethylsilylmethylallenes-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2006.07.013-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.47, no.36, pp.6353 - 6356-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume47-
dc.citation.number36-
dc.citation.startPage6353-
dc.citation.endPage6356-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000240090200005-
dc.identifier.scopusid2-s2.0-33746583095-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordAuthoracyliminium ion-
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