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dc.contributor.authorKarmakar, S.
dc.contributor.authorChakrabarty, Manas
dc.date.accessioned2013-03-01T10:03:00Z
dc.date.available2013-03-01T10:03:00Z
dc.date.issued2008-02-01
dc.identifierFOR ACCESS / DOWNLOAD PROBLEM -- PLEASE CONTACT LIBRARIAN, BOSE INSTITUTE, akc@bic.boseinst.ernet.inen_US
dc.identifier.citationKcm11akar Sand Chakrabarty ;'vi (2008) Reaction ofdiethyl mc:soxalate with active methylene compounds: ;m intcrcsring mttconw. J Tndion Chem. Soc, 85_: 224--2?7.en_US
dc.identifier.issn0019-4522
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dc.identifier.uri2. Scopus : Citation Link ->en_US
dc.identifier.urihttp://www.scopus.com/record/display.url?eid=2-s2.0-40849098683&origin=resultslist&sort=plf-f&src=s&nlo=&nlr=&nls=&sid=968F17F5D840EFEA275A52117222E5B3.CnvicAmOODVwpVrjSeqQ%3a210&sot=aut&sdt=a&sl=38&s=AU-ID%28%22Chakrabarty%2c+Manas%22+7006688171%29&relpos=7&relpos=7&searchTerm=AU-ID%28\%26quot%3BChakrabarty%2C+Manas\%26quot%3B+7006688171%29#en_US
dc.description.abstractDiethyl mesoxalate reacts separately with each of Meldrum's acid, indan-1,3-dione and diethyl malonate - all active methylene compounds - on neutral alumina either at room temperature or under microwave irradiation to furnish expeditiously the corresponding tertiary carbinols in very good yields. However, when the reaction of diethyl mesoxalate with a number of other active methylene compounds was tried similarly or by heating at 60-70 degrees C, the reactions either led to single products, which were too unstable to be isolated, or simply failed. Our findings, shedding new light on the reactivity of diethyl mesoxalate, are presented below.en_US
dc.language.isoenen_US
dc.publisherSCIENTIFIC PUBL-INDIAen_US
dc.subjectdiethyl mesoxalateen_US
dc.subjectactive methylene compoundsen_US
dc.subjectneutral aluminaen_US
dc.subjecttert-carbinolsen_US
dc.titleReaction of diethyl mesoxalate with active methylene compounds: An interesting outcomeen_US
dc.title.alternativeJournal of the Indian Chemical Societyen_US
dc.typeArticleen_US


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