DSpace at KISTKIST ArticleOthers

Full metadata record

DC Field Value Language
dc.contributor.authorKOH, HY-
dc.contributor.authorKANG, HY-
dc.contributor.authorCHOI, KI-
dc.contributor.authorCHANG, MH-
dc.date.accessioned2024-01-22T00:10:46Z-
dc.date.available2024-01-22T00:10:46Z-
dc.date.created2022-01-11-
dc.date.issued1990-12-20-
dc.identifier.issn0253-2964-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/147009-
dc.description.abstractNew aminothiazolyl cephalosporins with alkoxyiminomethyl(2-aminothiazol-4-yl)acetyl substituents at 7-position of cephems were synthesized starting from (2-aminothiazol-4-yl)acetate via one carbon homologation followed by acylation with 7-aminoceph-3-em-4-carboxylic acid derivatives. These new aminothiazolyl cephalosporins exhibit promising in vitro activities against various strains including Gram positive bacteria.-
dc.languageEnglish-
dc.publisherKOREAN CHEMICAL SOC-
dc.titleNEW AMINOTHIAZOLYL CEPHALOSPORINS - SYNTHESIS AND BIOLOGICAL EVALUATION OF 7-[ALKOXYIMINOMETHYL(2-AMINOTHIAZOL-4-YL)ACETAMIDO]CEPH-3-EM-4-CARBOXYLI C ACIDS-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.11, no.6, pp.538 - 542-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume11-
dc.citation.number6-
dc.citation.startPage538-
dc.citation.endPage542-
dc.description.journalRegisteredClassscie-
dc.identifier.wosidA1990EV68600022-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
Appears in Collections:
KIST Article > Others
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML
Show Simple Item Record

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE