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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Park, T | - |
| dc.contributor.author | Mayer, MF | - |
| dc.contributor.author | Nakashima, S | - |
| dc.contributor.author | Zimmerman, SC | - |
| dc.date.accessioned | 2015-06-25T03:36:38Z | - |
| dc.date.available | 2015-06-25T03:36:38Z | - |
| dc.date.created | 2009-09-30 | - |
| dc.date.issued | 2005-06-01 | - |
| dc.identifier.issn | 0936-5214 | - |
| dc.identifier.other | 2015-OAK-0000016628 | en_US |
| dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/12960 | - |
| dc.description.abstract | A two-step conversion of 2-chloro-7-ainido-1,8-naplithyridine to 2.7-diamino-1,8-naphthyridine is described. The process, which involves a nucleophilic aromatic substitution reaction with 4-methoxybenzylamine and subsequent deprotection, can be carried out on a large scale. | - |
| 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 | PREPARATION OF 2,7-DIAMINO-1,8-NAPHTHYRIDINE: A USEFUL BUILDING BLOCK FOR SUPRAMOLECULAR CHEMISTRY | - |
| dc.type | Article | - |
| dc.contributor.college | 화학공학과 | en_US |
| dc.identifier.doi | 10.1055/S-2005-86850 | - |
| dc.author.google | Park, T | en_US |
| dc.author.google | Mayer, MF | en_US |
| dc.author.google | Zimmerman, SC | en_US |
| dc.author.google | Nakashima, S | en_US |
| dc.relation.volume | 9 | en_US |
| dc.relation.issue | 9 | en_US |
| dc.relation.startpage | 1435 | en_US |
| dc.relation.lastpage | 1436 | en_US |
| dc.contributor.id | 10148712 | 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, v.9, no.9, pp.1435 - 1436 | - |
| dc.identifier.wosid | 000229600000019 | - |
| dc.date.tcdate | 2019-01-01 | - |
| dc.citation.endPage | 1436 | - |
| dc.citation.number | 9 | - |
| dc.citation.startPage | 1435 | - |
| dc.citation.title | SYNLETT | - |
| dc.citation.volume | 9 | - |
| dc.contributor.affiliatedAuthor | Park, T | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.description.wostc | 20 | - |
| dc.type.docType | Article | - |
| dc.subject.keywordPlus | MULTIPLE HYDROGEN-BONDS | - |
| dc.subject.keywordPlus | DONOR-ACCEPTOR INTERACTION | - |
| dc.subject.keywordPlus | 1,8-NAPHTHYRIDINE DERIVATIVES | - |
| dc.subject.keywordPlus | HETEROCYCLIC UREAS | - |
| dc.subject.keywordPlus | HETERODIMERS | - |
| dc.subject.keywordPlus | ASSOCIATION | - |
| dc.subject.keywordPlus | STABILITY | - |
| dc.subject.keywordPlus | COMPLEX | - |
| dc.subject.keywordPlus | DIMERS | - |
| dc.subject.keywordAuthor | heterocycles | - |
| dc.subject.keywordAuthor | nucleophilic aromatic substitution | - |
| dc.subject.keywordAuthor | supramolecular systems | - |
| dc.subject.keywordAuthor | hydrogen bond | - |
| dc.subject.keywordAuthor | amine protecting group | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
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- 박태호PARK, TAIHO
- Dept. of Chemical Enginrg