Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/33942
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorFeng, L-
dc.creatorXu, L-
dc.creatorLam, K-
dc.creatorZhou, Z-
dc.creatorYip, CW-
dc.creatorChan, ASC-
dc.date.accessioned2015-06-23T09:14:40Z-
dc.date.available2015-06-23T09:14:40Z-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10397/33942-
dc.language.isoenen_US
dc.publisherPergamon Pressen_US
dc.subjectAldol reactionen_US
dc.subjectAmmonia solutionsen_US
dc.subjectMannich reactionen_US
dc.subjectTandemen_US
dc.titleDirect aldol and tandem Mannich reactions in room temperature ammonia solutionsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage8685-
dc.identifier.epage8689-
dc.identifier.volume46-
dc.identifier.issue50-
dc.identifier.doi10.1016/j.tetlet.2005.10.050-
dcterms.abstractAn economical, simple, and efficient direct aldol reaction via the double activation of both aldehydes and ketones by ammonia has been developed. An unprecedented tandem Mannich reaction was observed when hydroxybenzaldehydes, pyrrole-2-carboxyaldehyde, and indole-3-carboxyaldehyde were employed to afford 2,2-dimethyl-6-aryl-4-pyrilidinones in moderate to good yields.-
dcterms.bibliographicCitationTetrahedron letters, 2005, v. 46, no. 50, p. 8685-8689-
dcterms.isPartOfTetrahedron letters-
dcterms.issued2005-
dc.identifier.scopus2-s2.0-27744571730-
dc.identifier.eissn1873-3581-
dc.identifier.rosgroupidr26496-
dc.description.ros2005-2006 > Academic research: refereed > Publication in refereed journal-
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