Cited 7 time in
Pd-catalyzed oxa-[4+n] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Cho, Ho-Jun | - |
| dc.contributor.author | Kim, Ju Hyun | - |
| dc.date.accessioned | 2023-12-27T01:00:22Z | - |
| dc.date.available | 2023-12-27T01:00:22Z | - |
| dc.date.issued | 2023-12 | - |
| dc.identifier.issn | 1477-0520 | - |
| dc.identifier.issn | 1477-0539 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/69000 | - |
| dc.description.abstract | Transition metal-catalyzed dipolar cycloaddition is one of the most efficient and powerful synthetic strategies to produce diverse heterocycles. In particular, for the construction of oxygen-containing heterocycles, which are valuable structural motifs found in pharmaceuticals and natural compounds, transition metal-catalyzed oxa-dipolar cycloaddition using an oxygen-containing dipole has emerged as a promising method. In recent years, the 1,4-O/C dipole synthons 2-alkylidenetrimethylene carbonate and 2-hydroxymethylallyl carbonate have been developed and successfully applied to palladium-catalyzed oxa-[4 + n] dipolar cycloadditions with diverse dipolarophiles. In this review, we summarize recent advances in palladium-catalyzed oxa-[4 + n] dipolar cycloadditions using 1,4-O/C dipoles including asymmetric catalysis and divergent catalysis toward five- to nine-membered O-heterocycles. | - |
| dc.format.extent | 12 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Royal Society of Chemistry | - |
| dc.title | Pd-catalyzed oxa-[4+n] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1039/d3ob01619f | - |
| dc.identifier.scopusid | 2-s2.0-85178610503 | - |
| dc.identifier.wosid | 001109883800001 | - |
| dc.identifier.bibliographicCitation | Organic and Biomolecular Chemistry, v.21, no.48, pp 9507 - 9518 | - |
| dc.citation.title | Organic and Biomolecular Chemistry | - |
| dc.citation.volume | 21 | - |
| dc.citation.number | 48 | - |
| dc.citation.startPage | 9507 | - |
| dc.citation.endPage | 9518 | - |
| dc.type.docType | Review | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | RING-CLOSURE REACTIONS | - |
| dc.subject.keywordPlus | ASYMMETRIC-SYNTHESIS | - |
| dc.subject.keywordPlus | PALLADIUM | - |
| dc.subject.keywordPlus | TRIMETHYLENEMETHANE | - |
| dc.subject.keywordPlus | METHYLENETETRAHYDROFURANS | - |
| dc.subject.keywordPlus | ANNULATIONS | - |
| dc.subject.keywordPlus | CYCLIZATION | - |
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