Full metadata record
DC FieldValueLanguage
dc.contributor.authorLin, Wun-Hueien_US
dc.contributor.authorWu, Wen-Chunen_US
dc.contributor.authorSelvaraju, Manikandanen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2017-04-21T06:56:08Z-
dc.date.available2017-04-21T06:56:08Z-
dc.date.issued2017en_US
dc.identifier.issn2052-4129en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c6qo00733cen_US
dc.identifier.urihttp://hdl.handle.net/11536/133235-
dc.description.abstractA direct and unconventional method for the synthesis of benzazoles and quinazolinones is discovered by using iron pentacarbonyl as a reducing agent and a carbon monoxide source under microwave irradiation. The reaction of substituted aryl iodides with o-amino/mercapto/hydroxyl nitrobenzenes and o-nitrobenzamides successfully delivered a wide variety of benzazoles and quinazolinones, respectively.en_US
dc.language.isoen_USen_US
dc.titleOne-pot synthesis of benzazoles and quinazolinones via iron pentacarbonyl mediated carbonylation of aryl iodides under microwave irradiationen_US
dc.identifier.doi10.1039/c6qo00733cen_US
dc.identifier.journalORGANIC CHEMISTRY FRONTIERSen_US
dc.citation.volume4en_US
dc.citation.issue3en_US
dc.citation.spage392en_US
dc.citation.epage397en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000395904900011en_US
Appears in Collections:Articles