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dc.contributor.authorPayne, Alan
dc.date.accessioned2017-01-30T10:54:48Z
dc.date.available2017-01-30T10:54:48Z
dc.date.created2014-01-15T20:00:53Z
dc.date.issued2013
dc.identifier.citationPayne, Alan D. 2013. Photochemistry of 3H-furo[3,4-c]pyrazoles and 3H-thieno[3,4-c] pyrazoles. Tetrahedron. 69 (44): pp. 9316-9321.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/6704
dc.identifier.doi10.1016/j.tet.2013.08.022
dc.description.abstract

The first examples of 3H-furo [3,4-c]pyrazoles and 3H-thieno[3,4-c]pyrazoles were prepared in an attempt to isolate examples of cyclopropane-fused thiophenes and furans. Adducts of acetylenic ketones and 2-diazopropane were reacted with 10-camphorsulfonic acid or phosphorus pentasulfide to produce the title compounds. Photolysis of these compounds did not give the cyclopropane-fused products rather an unreported photochemical fragmentation was observed.

dc.publisherPergamon-Elsevier Science Ltd
dc.subjectPhotochemistry
dc.subject3H-Pyrazoles
dc.subjectCycloproparenes
dc.titlePhotochemistry of 3H-furo[3,4-c]pyrazoles and 3H-thieno[3,4-c] pyrazoles
dc.typeJournal Article
dcterms.source.volume69
dcterms.source.startPage9316
dcterms.source.endPage9321
dcterms.source.issn00404020
dcterms.source.titleTetrahedron
curtin.department
curtin.accessStatusFulltext not available


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