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

dc.contributor.author	Spivey, A.C
dc.contributor.author	Srikaran, R
dc.contributor.author	Diaper, C.M
dc.contributor.author	Turner, D.J
dc.date.accessioned	2014-02-05T18:00:17Z
dc.date.accessioned	2022-07-11T08:25:13Z
dc.date.available	2014-02-05T18:00:17Z
dc.date.available	2022-07-11T08:25:13Z
dc.date.issued	2003-05
dc.identifier.issn	14770520
dc.identifier.uri	http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/246
dc.description.abstract	The 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.language.iso	en	en_US
dc.title	Traceless solid phase synthesis of 2-substituted pyrimidines using an 'off-the-shelf' chlorogermane-functionalised resin	en_US
dc.type	Article	en_US