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Synthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran

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dc.contributor.authorLee, Seung Hwan-
dc.contributor.authorKwon, Young Bum-
dc.contributor.authorYoon, Cheol Min-
dc.date.accessioned2021-09-09T01:06:38Z-
dc.date.available2021-09-09T01:06:38Z-
dc.date.created2021-06-10-
dc.date.issued2009-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/122126-
dc.description.abstract5-ortho-Carboranylsalicylaldehyde was prepared from 5-iodosalicylaldehyde in six steps in 18% overall yield, and also from 5-iodosalicylic acid in seven steps in 45% overall yield. The reaction of 5-ortho-carboranylsalicylaldehyde with Fischer's base gave a spiropyran in 63% yield.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectUNFUNCTIONALIZED OLEFINS-
dc.subjectAMINO-ACIDS-
dc.subjectEPOXIDATION-
dc.subjectCOUMARINS-
dc.titleSynthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, Cheol Min-
dc.identifier.doi10.1080/00397910902883694-
dc.identifier.scopusid2-s2.0-70350635519-
dc.identifier.wosid000272207000012-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.39, no.22, pp.4069 - 4078-
dc.relation.isPartOfSYNTHETIC COMMUNICATIONS-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume39-
dc.citation.number22-
dc.citation.startPage4069-
dc.citation.endPage4078-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusUNFUNCTIONALIZED OLEFINS-
dc.subject.keywordPlusAMINO-ACIDS-
dc.subject.keywordPlusEPOXIDATION-
dc.subject.keywordPlusCOUMARINS-
dc.subject.keywordAuthorCoumarin-
dc.subject.keywordAuthorindolinospirobenzopyran-
dc.subject.keywordAuthorortho-carborane-
dc.subject.keywordAuthorsalicylaldehyde-
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