Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/14510
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFokas, D.en
dc.contributor.authorBaldino, C. M.en
dc.date.accessioned2015-11-24T17:38:33Z-
dc.date.available2015-11-24T17:38:33Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/14510-
dc.rightsDefault Licence-
dc.subjectdiversity oriented synthesisen
dc.subjectindolazoninesen
dc.subjectpolycyclic indolic compoundsen
dc.subjectskeletal diversityen
dc.subjectsolution-phase chemistryen
dc.subjectbeta-tetrahydrocarbolinesen
dc.titleStrategies for the Synthesis of Novel Indole Alkaloid-Based Screening Libraries for Drug Discoveryen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI: 10.1007/s11030-005-1292-z-
heal.identifier.secondaryhttp://www.springerlink.com/content/r25t7677j4357k61/-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικώνel
heal.publicationDate2005-
heal.abstractA series of diverse indole-based chemotypes were synthesized from beta-tetrahydrocarboline (beta-THC) scaffolds prepared from commercially and readily available tryptamines and agr-ketoesters. Diversity can be generated within these chemotypes through the following strategies: (a) appendage of substituents to the beta-THC scaffold, prepared in situ or as a template, through further elaboration and (b) skeletal modifications to the beta-THC scaffold via ring forming or ring breaking reactions. The strategies described here are amenable to high throughput solution-phase parallel synthesis, providing access to novel indole-based screening libraries for drug discovery.en
heal.publisherSpringerLinken
heal.journalNameMolecular Diversityen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

Files in This Item:
File Description SizeFormat 
Fokas-2005-Str.pdf2.06 MBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons