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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | AHN, KH | - |
| dc.contributor.author | HAN, DS | - |
| dc.contributor.author | JIN, CS | - |
| dc.contributor.author | KANG, DH | - |
| dc.contributor.author | KIM, DH | - |
| dc.contributor.author | KIM, JS | - |
| dc.contributor.author | SHIN, YS | - |
| dc.date.accessioned | 2015-06-25T03:36:28Z | - |
| dc.date.available | 2015-06-25T03:36:28Z | - |
| dc.date.created | 2009-08-12 | - |
| dc.date.issued | 1992-04 | - |
| dc.identifier.issn | 0936-5214 | - |
| dc.identifier.other | 2015-OAK-0000008572 | en_US |
| dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/12955 | - |
| dc.description.abstract | Treatment of trans-2,3-epoxy alcohols 1, activated by triethylaluminum, with arylaluminum complexes 3 caused a regioselective ring-opening reaction at the 3-position to yield 3-aryl-1,2-alkanediols 4 in moderate yields. The activation of the epoxY ring by coordination with a Lewis acid appears to be essential for obtaining the desired product in a reasonable yield. While bulky substituents at the 3-position lowered the regioselectivity, a methoxy or methylenedioxy moiety on the arylaluminum complex 3 improved the regioselectivity drastically. | - |
| dc.description.statementofresponsibility | open | en_US |
| dc.language | English | - |
| dc.publisher | GEORG THIEME VERLAG KG | - |
| dc.relation.isPartOf | SYNLETT | - |
| dc.rights | BY_NC_ND | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.0/kr | en_US |
| dc.title | REGIOSELECTIVE OXIRANE RING-OPENING OF TRANS-2,3-EPOXY ALCOHOLS WITH ARYLALUMINUM COMPLEXES | - |
| dc.type | Article | - |
| dc.contributor.college | 분자소재융합계의 전자-광 거동연구센터 | en_US |
| dc.author.google | AHN, KH | en_US |
| dc.author.google | HAN, DS | en_US |
| dc.author.google | SHIN, YS | en_US |
| dc.author.google | KIM, JS | en_US |
| dc.author.google | KIM, DH | en_US |
| dc.author.google | KANG, DH | en_US |
| dc.author.google | JIN, CS | en_US |
| dc.relation.startpage | 306 | en_US |
| dc.relation.lastpage | 308 | en_US |
| dc.contributor.id | 10087916 | en_US |
| dc.relation.journal | SYNLETT | en_US |
| dc.relation.index | SCI급, SCOPUS 등재논문 | en_US |
| dc.relation.sci | SCI | en_US |
| dc.collections.name | Journal Papers | en_US |
| dc.type.rims | ART | - |
| dc.identifier.bibliographicCitation | SYNLETT, no.4, pp.306 - 308 | - |
| dc.identifier.wosid | A1992HQ58100017 | - |
| dc.citation.endPage | 308 | - |
| dc.citation.number | 4 | - |
| dc.citation.startPage | 306 | - |
| dc.citation.title | SYNLETT | - |
| dc.contributor.affiliatedAuthor | AHN, KH | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.description.wostc | 8 | - |
| dc.type.docType | Note | - |
| dc.subject.keywordPlus | 2,3-EPOXY ALCOHOLS | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordPlus | REAGENTS | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.relation.journalResearchArea | Chemistry | - |
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Related Researcher
- 안교한AHN, KYO HAN
- Dept of Chemistry