Synthesis of multi-substituted pyrazoles utilizing the N-alkylated 3-hydroxy-3-propargyl- or allenylisoindolines

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dc.contributor.authorChoi, YHko
dc.contributor.authorKim, KSko
dc.contributor.authorLee, Sko
dc.contributor.authorJeong, TSko
dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorKim, YHko
dc.contributor.authorLee, WSko
dc.date.accessioned2013-03-04T03:47:18Z-
dc.date.available2013-03-04T03:47:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2003-11-
dc.identifier.citationHETEROCYCLES, v.60, no.11, pp.2499 - 2510-
dc.identifier.issn0385-5414-
dc.identifier.urihttp://hdl.handle.net/10203/81795-
dc.description.abstractN-Alkyl-substituted phthalimides (1) were easily converted to di-, tri-, and tetra-substituted pyrazoles (10) via a one-pot addition-decyclization-cyclocondensation process. Then, the structure and the position of N1-substitution of the 1,3-pyrazole ring were determined by X-Ray crystallographic analysis and (1)HnOe experiments.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectALLENYL KETONES-
dc.subjectCYCLIZATION-
dc.titleSynthesis of multi-substituted pyrazoles utilizing the N-alkylated 3-hydroxy-3-propargyl- or allenylisoindolines-
dc.typeArticle-
dc.identifier.wosid000186251300009-
dc.identifier.scopusid2-s2.0-0142027266-
dc.type.rimsART-
dc.citation.volume60-
dc.citation.issue11-
dc.citation.beginningpage2499-
dc.citation.endingpage2510-
dc.citation.publicationnameHETEROCYCLES-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorChoi, YH-
dc.contributor.nonIdAuthorKim, KS-
dc.contributor.nonIdAuthorLee, S-
dc.contributor.nonIdAuthorJeong, TS-
dc.contributor.nonIdAuthorKim, YH-
dc.contributor.nonIdAuthorLee, WS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusALLENYL KETONES-
dc.subject.keywordPlusCYCLIZATION-
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