Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/24359
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorZhang, SL-
dc.creatorHuang, ZS-
dc.creatorShen, YD-
dc.creatorLi, YM-
dc.creatorYao, JH-
dc.creatorHuang, M-
dc.creatorChan, ASC-
dc.creatorGu, LQ-
dc.date.accessioned2015-06-23T09:15:13Z-
dc.date.available2015-06-23T09:15:13Z-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10397/24359-
dc.language.isoenen_US
dc.publisherPergamon Pressen_US
dc.subject1,4-Benzoquinoneen_US
dc.subject4-Hydroxycoumarinsen_US
dc.subjectMichael additionen_US
dc.titleThe unique regioselectivity in the formation of disubstituted-1,4-benzoquinones generated from the reaction of 4-hydroxycoumarins with 1,4-benzoquinoneen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage6757-
dc.identifier.epage6760-
dc.identifier.volume47-
dc.identifier.issue38-
dc.identifier.doi10.1016/j.tetlet.2006.07.076-
dcterms.abstractThe 2,3-disubstituted 1,4-benzoquinones were synthesized through the regioselective addition of 4-hydroxycoumarins with 1,4-benzoquinone in aqueous acetone, which were different from 2,5-disubstituted adducts generated by the previously reported reaction of compounds possessing an activated methylene with 1,4-benzoquinone.-
dcterms.bibliographicCitationTetrahedron letters, 2006, v. 47, no. 38, p. 6757-6760-
dcterms.isPartOfTetrahedron letters-
dcterms.issued2006-
dc.identifier.isiWOS:000240670800012-
dc.identifier.scopus2-s2.0-33747173040-
dc.identifier.eissn1873-3581-
dc.identifier.rosgroupidr30639-
dc.description.ros2006-2007 > Academic research: refereed > Publication in refereed journal-
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