Article
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jeong, W | - |
| dc.contributor.author | Lee, JH | - |
| dc.contributor.author | Kim, J | - |
| dc.contributor.author | Lee, WJ | - |
| dc.contributor.author | Seong, JH | - |
| dc.contributor.author | Park, J | - |
| dc.contributor.author | RHEE, YOUNG HO | - |
| dc.date.accessioned | 2016-03-31T07:57:25Z | - |
| dc.date.available | 2016-03-31T07:57:25Z | - |
| dc.date.created | 2015-01-22 | - |
| dc.date.issued | 2014-04 | - |
| dc.identifier.issn | 2046-2069 | - |
| dc.identifier.other | 2014-OAK-0000030769 | - |
| dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/14242 | - |
| dc.description.abstract | A new synthetic method for homopropargylic amines from alkyl azides is presented. A salient feature of this reaction is the involvement of N-unsubstituted imines as the key intermediates, which are generated from alkyl azides by Ru catalysis under photolytic conditions. Notably, this method avoids the use of a protective group strategy in the homopropargylic amine synthesis. | - |
| dc.description.statementofresponsibility | X | - |
| dc.language | English | - |
| dc.publisher | Royal Society of Chemistry | - |
| dc.relation.isPartOf | RSC Advances | - |
| dc.title | A Ru-catalyzed one-pot synthesis of homopropargylic amines from alkyl azides under photolytic conditions | - |
| dc.type | Article | - |
| dc.contributor.college | 화학과 | - |
| dc.identifier.doi | 10.1039/C4RA02941K | - |
| dc.relation.volume | 4 | - |
| dc.relation.issue | 40 | - |
| dc.relation.startpage | 20632 | - |
| dc.relation.lastpage | 20635 | - |
| dc.contributor.id | 10075891 | - |
| dc.relation.journal | RSC Advances | - |
| dc.relation.index | SCI급, SCOPUS 등재논문 | - |
| dc.relation.sci | SCI | - |
| dc.collections.name | Journal Papers | - |
| dc.type.rims | ART | - |
| dc.identifier.bibliographicCitation | RSC Advances, v.4, no.40, pp.20632 - 20635 | - |
| dc.identifier.wosid | 000336833400004 | - |
| dc.date.tcdate | 2019-01-01 | - |
| dc.citation.endPage | 20635 | - |
| dc.citation.number | 40 | - |
| dc.citation.startPage | 20632 | - |
| dc.citation.title | RSC Advances | - |
| dc.citation.volume | 4 | - |
| dc.contributor.affiliatedAuthor | Park, J | - |
| dc.contributor.affiliatedAuthor | RHEE, YOUNG HO | - |
| dc.identifier.scopusid | 2-s2.0-84901317339 | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.description.wostc | 13 | - |
| dc.description.scptc | 12 | * |
| dc.date.scptcdate | 2018-05-121 | * |
| dc.type.docType | Article | - |
| dc.subject.keywordPlus | CARBONYL-COMPOUNDS | - |
| dc.subject.keywordPlus | STEREOSELECTIVE-SYNTHESIS | - |
| dc.subject.keywordPlus | ASYMMETRIC-SYNTHESIS | - |
| dc.subject.keywordPlus | IMINES | - |
| dc.subject.keywordPlus | CYCLOISOMERIZATION | - |
| dc.subject.keywordPlus | ALLYLATION | - |
| dc.subject.keywordPlus | EFFICIENT | - |
| dc.subject.keywordPlus | ALCOHOLS | - |
| dc.subject.keywordPlus | ALLENYLBORATION | - |
| dc.subject.keywordPlus | PROPARGYLATION | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
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Related Researcher
- 이영호RHEE, YOUNG HO
- Dept of Chemistry