Solution-phase combinatorial synthesis of isoxazolines and isoxazoles using [2+3] cycloaddition reaction of nitrile oxides

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dc.contributor.authorKang, KHko
dc.contributor.authorPae, ANko
dc.contributor.authorIl Choi, Kko
dc.contributor.authorCho, YSko
dc.contributor.authorChung, BYko
dc.contributor.authorLee, JEko
dc.contributor.authorJung, SHko
dc.contributor.authorKoh, HYko
dc.contributor.authorLee, Hee Yoonko
dc.date.accessioned2013-03-03T21:01:51Z-
dc.date.available2013-03-03T21:01:51Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-02-
dc.identifier.citationTETRAHEDRON LETTERS, v.42, no.6, pp.1057 - 1060-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/80417-
dc.description.abstractAn efficient way to construct a library of isoxazoles and isoxazolines was developed by solution-phase 1,3-dipolar cycloaddition reaction of nitrile oxides with olefins and alkynes followed by precipitation of the products as HCl salts. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleSolution-phase combinatorial synthesis of isoxazolines and isoxazoles using [2+3] cycloaddition reaction of nitrile oxides-
dc.typeArticle-
dc.identifier.wosid000166894400023-
dc.identifier.scopusid2-s2.0-0035808917-
dc.type.rimsART-
dc.citation.volume42-
dc.citation.issue6-
dc.citation.beginningpage1057-
dc.citation.endingpage1060-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorKang, KH-
dc.contributor.nonIdAuthorPae, AN-
dc.contributor.nonIdAuthorIl Choi, K-
dc.contributor.nonIdAuthorCho, YS-
dc.contributor.nonIdAuthorChung, BY-
dc.contributor.nonIdAuthorLee, JE-
dc.contributor.nonIdAuthorJung, SH-
dc.contributor.nonIdAuthorKoh, HY-
dc.type.journalArticleArticle-
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