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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

Diastereoselective Addition of Organolithiums to New Chiral Hydrazones. Enantioselective Synthesis of (R)- Coniine

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dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-28T02:55:53Z-
dc.date.available2013-02-28T02:55:53Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1996-07-
dc.identifier.citationTETRAHEDRON LETTERS, v.37, no.31, pp.5543 - 5546-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/72401-
dc.description.abstractThe reactions of organolithiums with the new chiral hydrazones derived from (S)-indoline-2-carboxylic acid afforded chiral hydrazines with Ugh diastereoselectivities (up to 99% de) and the present method was utilized for the preparation of high optically pure (R)-coniine (94% se). Copyright (C) 1996 Elsevier Science Ltd-
dc.languageEnglish-
dc.publisherPergamon-Elsevier Science Ltd-
dc.subjectALDEHYDE-SAMP HYDRAZONES-
dc.subjectALPHA-AMINO ACIDS-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subjectDIASTEREOFACIAL SELECTIVITY-
dc.subjectGRIGNARD-REAGENTS-
dc.subjectPIPERIDINES-
dc.subjectALKALOIDS-
dc.subjectIMINES-
dc.subjectORGANOMETALLICS-
dc.subject(-)-CONIINE-
dc.titleDiastereoselective Addition of Organolithiums to New Chiral Hydrazones. Enantioselective Synthesis of (R)- Coniine-
dc.typeArticle-
dc.identifier.wosidA1996UZ67600031-
dc.identifier.scopusid2-s2.0-0030605816-
dc.type.rimsART-
dc.citation.volume37-
dc.citation.issue31-
dc.citation.beginningpage5543-
dc.citation.endingpage5546-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusALDEHYDE-SAMP HYDRAZONES-
dc.subject.keywordPlusALPHA-AMINO ACIDS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusDIASTEREOFACIAL SELECTIVITY-
dc.subject.keywordPlusGRIGNARD-REAGENTS-
dc.subject.keywordPlusPIPERIDINES-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusIMINES-
dc.subject.keywordPlusORGANOMETALLICS-
dc.subject.keywordPlus(-)-CONIINE-
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