Traceless solid phase synthesis of 2-substituted pyrimidines using an 'off-the-shelf' chlorogermane-functionalised resin

dc.contributor.authorSpivey, A.C.
dc.contributor.authorSrikaran, R.
dc.contributor.authorDiaper, C.M.
dc.contributor.authorTurner, D.J.
dc.date.accessioned2014-02-05T18:00:17Z
dc.date.accessioned2022-07-11T08:25:13Z
dc.date.available2014-02-05T18:00:17Z
dc.date.available2022-07-11T08:25:13Z
dc.date.issued2003-05
dc.description.abstractThe parallel solid phase synthesis of an 18-member library of 2-substituted pyrimidines is described using a chlorogermane-functionalised resin. The success of the key Pinner-type condensations between a resin-bound enaminone and an array of amidine hydrochlorides highlights the stability of arylgermane linkers (cf. arylsilanes) towards strongly basic/nucleophilic conditions.en_US
dc.identifier.issn14770520
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/246
dc.language.isoenen_US
dc.titleTraceless solid phase synthesis of 2-substituted pyrimidines using an 'off-the-shelf' chlorogermane-functionalised resinen_US
dc.typeArticleen_US

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