Cited 8 time in
Recent Advances in Synthetic Methods for 2H-Pyrroles
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Choi, Seoung-Mi | - |
| dc.contributor.author | Kim, Ju Hyun | - |
| dc.date.accessioned | 2023-12-18T06:30:42Z | - |
| dc.date.available | 2023-12-18T06:30:42Z | - |
| dc.date.issued | 2024-01 | - |
| dc.identifier.issn | 1615-4150 | - |
| dc.identifier.issn | 1615-4169 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/68978 | - |
| dc.description.abstract | The compound, 2H-pyrrole, is a key scaffold contained in natural products, bioactive compounds, pharmaceuticals, and organic functional materials. However, the development of efficient synthetic strategies for 2H-pyrroles is challenging. This is because 2H-pyrroles, owing to their nonaromatic nature, are easily converted into the thermodynamically more stable 1H-pyrroles. Recently, efficient and straightforward synthetic strategies for 2H-pyrroles have been developed, including the dearomatization of 1H-pyrrole, oxidation of pyrrolines or pyrrolidines, ring construction via catalytic cycloaddition, and rearrangement of 3H-pyrroles. In this review, we summarize the progress in the research on 2H-pyrrole synthesis since 2000 and briefly discuss the synthesis reaction mechanisms. © 2023 Wiley-VCH GmbH. | - |
| dc.format.extent | 16 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | John Wiley and Sons Inc | - |
| dc.title | Recent Advances in Synthetic Methods for 2H-Pyrroles | - |
| dc.type | Article | - |
| dc.publisher.location | 독일 | - |
| dc.identifier.doi | 10.1002/adsc.202301238 | - |
| dc.identifier.scopusid | 2-s2.0-85178964875 | - |
| dc.identifier.wosid | 001115667600001 | - |
| dc.identifier.bibliographicCitation | Advanced Synthesis and Catalysis, v.366, no.1, pp 2 - 17 | - |
| dc.citation.title | Advanced Synthesis and Catalysis | - |
| dc.citation.volume | 366 | - |
| dc.citation.number | 1 | - |
| dc.citation.startPage | 2 | - |
| dc.citation.endPage | 17 | - |
| dc.type.docType | Review | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Applied | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | ASYMMETRIC ALLYLIC DEAROMATIZATION | - |
| dc.subject.keywordPlus | POSITIVE HALOGEN COMPOUNDS | - |
| dc.subject.keywordPlus | VI CARBENE COMPLEXES | - |
| dc.subject.keywordPlus | ENANTIOSELECTIVE SYNTHESIS | - |
| dc.subject.keywordPlus | TRIVALENT PHOSPHORUS | - |
| dc.subject.keywordPlus | AZOMETHINE YLIDES | - |
| dc.subject.keywordPlus | 3+2 CYCLOADDITION | - |
| dc.subject.keywordPlus | NITRILE YLIDES | - |
| dc.subject.keywordPlus | PYRROLES | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordAuthor | 2H-pyrrole | - |
| dc.subject.keywordAuthor | Asymmetric catalysis | - |
| dc.subject.keywordAuthor | Non-aromatic heterocycles | - |
| dc.subject.keywordAuthor | Organocatalysis | - |
| dc.subject.keywordAuthor | Transition metal catalysis | - |
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