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One pot catalytic NO2 reduction, ring hydrogenation, and N-alkylation from nitroarenes to generate alicyclic amines using Ru/C-NaNO2
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Oh, Seung Geun | - |
| dc.contributor.author | Mishra, Vivek | - |
| dc.contributor.author | Cho, Jin Ku | - |
| dc.contributor.author | Kim, Baek-Jin | - |
| dc.contributor.author | Kim, Hoon Sik | - |
| dc.contributor.author | Suh, Young-Woong | - |
| dc.contributor.author | Lee, Hyunjoo | - |
| dc.contributor.author | Park, Ho Seok | - |
| dc.contributor.author | Kim, Yong Jin | - |
| dc.date.accessioned | 2022-07-16T06:30:26Z | - |
| dc.date.available | 2022-07-16T06:30:26Z | - |
| dc.date.issued | 2014-01 | - |
| dc.identifier.issn | 1566-7367 | - |
| dc.identifier.issn | 1873-3905 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160950 | - |
| dc.description.abstract | A report to produce alicyclic amines and subsequent N-alkylation with alcohols using Ru/C-NaNO2 catalyzed facile transformation of nitrobenzene was investigated. Effects of solvent, temperature, pressure, reaction time, and molar-ratio of substrate/catalyst on product composition were also studied. These mechanistic studies explain that nitrobenzene undergoes hydrogenation reaction in the following order; -NO2 reduction to -NH2, aromatic ring-hydrogenation to alicyclic, and from the reaction of alcohol to give N-alkylated amines. This investigation shed lights on possible application to polyurethane chemistry since these amines are used as important precursors for diisocyanates. | - |
| dc.format.extent | 5 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Elsevier BV | - |
| dc.title | One pot catalytic NO2 reduction, ring hydrogenation, and N-alkylation from nitroarenes to generate alicyclic amines using Ru/C-NaNO2 | - |
| dc.type | Article | - |
| dc.publisher.location | 네델란드 | - |
| dc.identifier.doi | 10.1016/j.catcom.2013.09.012 | - |
| dc.identifier.scopusid | 2-s2.0-84884923631 | - |
| dc.identifier.wosid | 000328527000018 | - |
| dc.identifier.bibliographicCitation | Catalysis Communications, v.43, pp 79 - 83 | - |
| dc.citation.title | Catalysis Communications | - |
| dc.citation.volume | 43 | - |
| dc.citation.startPage | 79 | - |
| dc.citation.endPage | 83 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.subject.keywordPlus | METAL CATALYSTS | - |
| dc.subject.keywordPlus | CARBON-DIOXIDE | - |
| dc.subject.keywordPlus | ANILINE | - |
| dc.subject.keywordPlus | NITROBENZENE | - |
| dc.subject.keywordPlus | ALCOHOLS | - |
| dc.subject.keywordPlus | CYCLOHEXYLAMINE | - |
| dc.subject.keywordPlus | COMPLEX | - |
| dc.subject.keywordPlus | WATER | - |
| dc.subject.keywordAuthor | Hydrogenation | - |
| dc.subject.keywordAuthor | Nitrobenzene | - |
| dc.subject.keywordAuthor | Cyclohexylamine | - |
| dc.subject.keywordAuthor | Ruthenium catalyst | - |
| dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S1566736713003488?via%3Dihub | - |
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