Highly diastereoselective addition of trimethylsilyl cyanide to chiral hydrazones in the presence of Et(2)AlCl

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dc.contributor.authorChoi, JYko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-28T06:15:58Z-
dc.date.available2013-02-28T06:15:58Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1996-10-
dc.identifier.citationTETRAHEDRON LETTERS, v.37, no.43, pp.7795 - 7796-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/73189-
dc.description.abstractChiral hydrazones, synthesized from (S)-1-amino-2-methoxymethylindoline and aliphatic aldehydes, reacted with trimethylsilyl cyanide in the presence of diethylaluminium chloride in CH2Cl2 at -78 degrees C to give chiral alpha-hydrazinonitriles with high diastereoselectivity (up to 96% de). Copyright (C) 1996 Elsevier Science Ltd.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectAMINO-ACIDS-
dc.subjectSTRECKER SYNTHESIS-
dc.subjectSCHIFF-BASES-
dc.titleHighly diastereoselective addition of trimethylsilyl cyanide to chiral hydrazones in the presence of Et(2)AlCl-
dc.typeArticle-
dc.identifier.wosidA1996VN16200039-
dc.type.rimsART-
dc.citation.volume37-
dc.citation.issue43-
dc.citation.beginningpage7795-
dc.citation.endingpage7796-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.identifier.doi10.1016/0040-4039(96)01780-7-
dc.contributor.nonIdAuthorChoi, JY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusAMINO-ACIDS-
dc.subject.keywordPlusSTRECKER SYNTHESIS-
dc.subject.keywordPlusSCHIFF-BASES-
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