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dc.contributor.authorChan, J.
dc.contributor.authorHoyle, C.
dc.contributor.authorLowe, Andrew
dc.date.accessioned2017-01-30T13:51:02Z
dc.date.available2017-01-30T13:51:02Z
dc.date.created2016-09-12T08:36:42Z
dc.date.issued2009
dc.identifier.citationChan, J. and Hoyle, C. and Lowe, A. 2009. Sequential phosphine-catalyzed, nucleophilic thiol ene/radical-mediated thiol-yne reactions and the facile orthogonal synthesis of polyfunctional materials. Journal of the American Chemical Society. 131 (16): pp. 5751-5753.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/35667
dc.identifier.doi10.1021/ja8099135
dc.description.abstract

The first example of highly efficient sequential thiol-ene/thiol-yne reactions conducted in an orthogonal manner is presented and its broad application in the synthesis of polyfunctional materials demonstrated. The anionic chain mechanism of the phosphine-mediated thiol-ene reaction is highlighted, as is the radical-mediated thiol-yne reaction. Kinetic data for a model reaction are presented, followed by a discussion of the synthesis of a range of materials with diverse functionality, including an example of potential biomedical significance. © 2009 American Chemical Society.

dc.publisherAmerican Chemical Society
dc.titleSequential phosphine-catalyzed, nucleophilic thiol ene/radical-mediated thiol-yne reactions and the facile orthogonal synthesis of polyfunctional materials
dc.typeJournal Article
dcterms.source.volume131
dcterms.source.number16
dcterms.source.startPage5751
dcterms.source.endPage5753
dcterms.source.issn0002-7863
dcterms.source.titleJournal of the American Chemical Society
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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