Stereoselective total synthesis of the natural (+)-lasonolide A

Cited 22 time in webofscience Cited 23 time in scopus
  • Hit : 376
  • Download : 0
DC FieldValueLanguage
dc.contributor.authorKang, SungHoko
dc.contributor.authorKang, SYko
dc.contributor.authorChoi, HWko
dc.contributor.authorKim, CMko
dc.contributor.authorJun, HSko
dc.contributor.authorYoun, JHko
dc.date.accessioned2013-03-04T14:31:01Z-
dc.date.available2013-03-04T14:31:01Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-05-
dc.identifier.citationSYNTHESIS-STUTTGART, v.25, no.7, pp.1102 - 1114-
dc.identifier.issn0039-7881-
dc.identifier.urihttp://hdl.handle.net/10203/82954-
dc.description.abstractThe natural (+)-lasonolide A (1), an anti-tumor agent, has been synthesized via thermodynamic benzylidene formation at the C-22 quaternary chiral center, use of a disulfone equivalent for elongation of the C-15-C-17 three-carbon chain as well as introduction of the two trans olefins at C-15 and C-17, iodocyclization for the upper THP, Michael addition for the bottom THP, and intramolecular Horner-Emmons olefination for the 20-membered macrolactone.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectLASONOLIDE-A-
dc.subjectSTEREOCONTROLLED SYNTHESIS-
dc.subjectHOMOALLYLIC ALCOHOLS-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subjectHYDROXY FUNCTIONS-
dc.subjectPROTECTING GROUPS-
dc.subjectCHIRAL SYNTHESIS-
dc.subjectMACROLIDE-
dc.subjectMACROCYCLIZATION-
dc.subjectOLEFINATION-
dc.titleStereoselective total synthesis of the natural (+)-lasonolide A-
dc.typeArticle-
dc.identifier.wosid000221429700025-
dc.type.rimsART-
dc.citation.volume25-
dc.citation.issue7-
dc.citation.beginningpage1102-
dc.citation.endingpage1114-
dc.citation.publicationnameSYNTHESIS-STUTTGART-
dc.identifier.doi10.1055/s-2004-822340-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorKang, SY-
dc.contributor.nonIdAuthorChoi, HW-
dc.contributor.nonIdAuthorKim, CM-
dc.contributor.nonIdAuthorJun, HS-
dc.contributor.nonIdAuthorYoun, JH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorasymmetric synthesis-
dc.subject.keywordAuthordiastereomeric differentiation-
dc.subject.keywordAuthormacrocyclization-
dc.subject.keywordAuthornatural products-
dc.subject.keywordAuthortotal synthesis-
dc.subject.keywordPlusLASONOLIDE-A-
dc.subject.keywordPlusSTEREOCONTROLLED SYNTHESIS-
dc.subject.keywordPlusHOMOALLYLIC ALCOHOLS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusHYDROXY FUNCTIONS-
dc.subject.keywordPlusPROTECTING GROUPS-
dc.subject.keywordPlusCHIRAL SYNTHESIS-
dc.subject.keywordPlusMACROLIDE-
dc.subject.keywordPlusMACROCYCLIZATION-
dc.subject.keywordPlusOLEFINATION-
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 22 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0