Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process
DC Field | Value | Language |
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dc.contributor.author | Kim, Gyeong Un | - |
dc.contributor.author | Cho, Hyunmi | - |
dc.contributor.author | Lee, Jae Kyun | - |
dc.contributor.author | Lee, Jae Yeol | - |
dc.contributor.author | Tae, Jinsung | - |
dc.contributor.author | Min, Sun-Joon | - |
dc.contributor.author | Kang, Taek | - |
dc.contributor.author | Cho, Yong Seo | - |
dc.date.accessioned | 2023-01-25T09:15:28Z | - |
dc.date.available | 2023-01-25T09:15:28Z | - |
dc.date.issued | 2022-12 | - |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.issn | 1364-548X | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111430 | - |
dc.description.abstract | We report the stereocontrolled synthesis of 1,6-diazecanes via a tandem aza-Prins type reaction of N-acyliminium ions with allylsilanes. It involves an aza-Prins type dimerization and cyclization in a single-step operation. This reaction represents the first example of 10-membered N-heterocycle synthesis using an aza-Prins reaction. Also, the interesting formation of an unusual tetracyclic compound through further cyclization of 1,6-diazecane and bicyclic compounds by the intramolecular cyclization of linear allylsilane are described. This tandem aza-Prins protocol provides a new synthetic strategy for the direct synthesis of medium-sized nitrogen heterocycles. | - |
dc.format.extent | 4 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Royal Society of Chemistry | - |
dc.title | Stereoselective synthesis of 1,6-diazecanes by a tandem aza-Prins type dimerization and cyclization process | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1039/d2cc05133h | - |
dc.identifier.scopusid | 2-s2.0-85143963574 | - |
dc.identifier.wosid | 000893488000001 | - |
dc.identifier.bibliographicCitation | Chemical Communications, v.59, no.1, pp 82 - 85 | - |
dc.citation.title | Chemical Communications | - |
dc.citation.volume | 59 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 82 | - |
dc.citation.endPage | 85 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.subject.keywordPlus | MEDIUM-SIZED RINGS | - |
dc.subject.keywordPlus | SCAFFOLD | - |
dc.subject.keywordPlus | DIKETOPIPERAZINE | - |
dc.subject.keywordPlus | HETEROCYCLES | - |
dc.subject.keywordPlus | DERIVATIVES | - |
dc.subject.keywordPlus | DIVERSITY | - |
dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2023/cc/d2cc05133h | - |
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