WEB OF SCIENCE
SCOPUS
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Gun Ha | - |
| dc.contributor.author | Jeon, Ji Hwan | - |
| dc.contributor.author | Jung, Byunghyuck | - |
| dc.contributor.author | Rohde, Jan-Uwe | - |
| dc.contributor.author | Hong, Sung You | - |
| dc.date.accessioned | 2025-07-03T09:40:09Z | - |
| dc.date.available | 2025-07-03T09:40:09Z | - |
| dc.date.created | 2025-06-30 | - |
| dc.date.issued | 2025-08 | - |
| dc.identifier.issn | 0936-5214 | - |
| dc.identifier.uri | https://scholar.dgist.ac.kr/handle/20.500.11750/58586 | - |
| dc.description.abstract | In this Account, we describe our recent research progress in the development of the functionalization of unsaturated substrates catalyzed by low-valent nickel. In particular, we discuss nickel-catalyzed azide–alkyne cycloaddition (NiAAC), [2 + 2 + 2] cycloaddition of diynes and nitriles, hydrosilylation of alkynes, and dicarbofunctionalization of 1,3-enynes. Moreover, we highlight our mechanistic studies aimed at elucidating catalytically active nickel intermediates, thereby contributing to the understanding and expansion of nickel-catalyzed synthetic methodologies. © 2025. Thieme. All rights reserved. | - |
| dc.language | English | - |
| dc.publisher | Thieme | - |
| dc.title | Regioselective Transformations of Unsaturated Systems Catalyzed by Low-Valent Nickel: Cycloaddition, Hydrosilylation, and Dicarbofunctionalization | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1055/a-2591-9299 | - |
| dc.identifier.wosid | 001510036700001 | - |
| dc.identifier.scopusid | 2-s2.0-105008706762 | - |
| dc.identifier.bibliographicCitation | Synlett, v.36, no.13, pp.1889 - 1899 | - |
| dc.description.isOpenAccess | FALSE | - |
| dc.subject.keywordAuthor | cycloaddition | - |
| dc.subject.keywordAuthor | unsaturated systems | - |
| dc.subject.keywordAuthor | hydrosilylation | - |
| dc.subject.keywordAuthor | dicarbofunctionalization | - |
| dc.subject.keywordAuthor | regioselectivity | - |
| dc.subject.keywordAuthor | reaction mechanisms | - |
| dc.subject.keywordAuthor | nickel | - |
| dc.subject.keywordPlus | COUPLING REACTIONS | - |
| dc.subject.keywordPlus | TERMINAL ALKYNES | - |
| dc.subject.keywordPlus | C-C | - |
| dc.subject.keywordPlus | AIR | - |
| dc.subject.keywordPlus | 1,4-ALKYLARYLATION | - |
| dc.subject.keywordPlus | 1,3-ENYNES | - |
| dc.subject.keywordPlus | REACTIVITY | - |
| dc.subject.keywordPlus | COMPLEXES | - |
| dc.subject.keywordPlus | PALLADIUM | - |
| dc.subject.keywordPlus | AZIDE-ALKYNE CYCLOADDITION | - |
| dc.citation.endPage | 1899 | - |
| dc.citation.number | 13 | - |
| dc.citation.startPage | 1889 | - |
| dc.citation.title | Synlett | - |
| dc.citation.volume | 36 | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.type.docType | Article | - |
