AN ASYMMETRIC-SYNTHESIS OF A KEY INTERMEDIATE TO 1-BETA-METHYLCARBAPENEM ANTIBIOTICS

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dc.contributor.authorHANG, SHko
dc.contributor.authorLee, Hee-Seungko
dc.date.accessioned2013-02-28T00:29:08Z-
dc.date.available2013-02-28T00:29:08Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1995-09-
dc.identifier.citationTETRAHEDRON LETTERS, v.36, no.37, pp.6713 - 6716-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/71748-
dc.description.abstract1 beta-Methylcarbapenem 3 has been enantioselectively synthesized starting from ethoxyethyl ether 8 and methyl (R)-3-iodo-2-methylpropionate via the intramolecular 1,3-dipolar cycloaddition of nitrone 6, in which the requisite chiral centers were settled.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectSTEREOCONTROLLED SYNTHESIS-
dc.subjectHOMOENOLATE-
dc.subjectNITRONE-
dc.titleAN ASYMMETRIC-SYNTHESIS OF A KEY INTERMEDIATE TO 1-BETA-METHYLCARBAPENEM ANTIBIOTICS-
dc.typeArticle-
dc.identifier.wosidA1995RU28000036-
dc.identifier.scopusid2-s2.0-0029117325-
dc.type.rimsART-
dc.citation.volume36-
dc.citation.issue37-
dc.citation.beginningpage6713-
dc.citation.endingpage6716-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorLee, Hee-Seung-
dc.contributor.nonIdAuthorHANG, SH-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSTEREOCONTROLLED SYNTHESIS-
dc.subject.keywordPlusHOMOENOLATE-
dc.subject.keywordPlusNITRONE-
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CH-Journal Papers(저널논문)
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