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dc.contributor.authorKang, SB-
dc.contributor.authorAhn, EJ-
dc.contributor.authorKim, Y-
dc.contributor.authorKim, YH-
dc.date.accessioned2024-01-21T19:07:25Z-
dc.date.available2024-01-21T19:07:25Z-
dc.date.created2022-01-10-
dc.date.issued1996-12-23-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144197-
dc.description.abstractA convenient procedure for preparation of the title compound of greater than or equal to 99% ee starting from 1-(2,3-difluoro-6-nitrophenoxy)-2-propanone (3) is presented. The key reaction is the intramolecular cyclization reaction in the presence of zinc chloride. Copyright (C) 1996 Elsevier Science Ltd-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectOPTICALLY-ACTIVE OFLOXACIN-
dc.subjectANTIBACTERIAL ACTIVITIES-
dc.subjectCHEMISTRY-
dc.subjectYEAST-
dc.titleA facile synthesis of (S)-(-)-7,8-difluoro-3,4-dihydro-3-methyl-2H-1,4-benzoxazine by zinc chloride assisted Mitsunobu cyclization reaction-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(97)82952-8-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.37, no.52, pp.9317 - 9320-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume37-
dc.citation.number52-
dc.citation.startPage9317-
dc.citation.endPage9320-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996VZ20200015-
dc.identifier.scopusid2-s2.0-0030599670-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusOPTICALLY-ACTIVE OFLOXACIN-
dc.subject.keywordPlusANTIBACTERIAL ACTIVITIES-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusYEAST-
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