DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kang, SungHo | ko |
dc.contributor.author | Lee, SB | ko |
dc.date.accessioned | 2013-02-27T17:49:03Z | - |
dc.date.available | 2013-02-27T17:49:03Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1998-04 | - |
dc.identifier.citation | CHEMICAL COMMUNICATIONS, no.7, pp.761 - 762 | - |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.uri | http://hdl.handle.net/10203/69927 | - |
dc.description.abstract | A highly enantioselective total synthesis of (+)-furanomycin 24 has been achieved via the mercury cation-mediated cyclizations of gamma-hydroxy alkene 4 and homoallylic trichloroacetimidate 11 to install the trans-2,5-disubstituted tetrahydrofuran and the (alpha S)-amino acid side chain, respectively. | - |
dc.language | English | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.subject | (+)-POLYOXAMIC ACID | - |
dc.subject | ALLYLIC ALCOHOLS | - |
dc.subject | FURANOMYCIN | - |
dc.subject | REARRANGEMENT | - |
dc.subject | BIOSYNTHESIS | - |
dc.subject | MECHANISM | - |
dc.subject | REAGENTS | - |
dc.subject | ROUTES | - |
dc.title | Total synthesis of (+)-furanomycin | - |
dc.type | Article | - |
dc.identifier.wosid | 000073042400015 | - |
dc.type.rims | ART | - |
dc.citation.issue | 7 | - |
dc.citation.beginningpage | 761 | - |
dc.citation.endingpage | 762 | - |
dc.citation.publicationname | CHEMICAL COMMUNICATIONS | - |
dc.contributor.localauthor | Kang, SungHo | - |
dc.contributor.nonIdAuthor | Lee, SB | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | (+)-POLYOXAMIC ACID | - |
dc.subject.keywordPlus | ALLYLIC ALCOHOLS | - |
dc.subject.keywordPlus | FURANOMYCIN | - |
dc.subject.keywordPlus | REARRANGEMENT | - |
dc.subject.keywordPlus | BIOSYNTHESIS | - |
dc.subject.keywordPlus | MECHANISM | - |
dc.subject.keywordPlus | REAGENTS | - |
dc.subject.keywordPlus | ROUTES | - |
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