Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/8987
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dc.contributor.authorPasha, M A-
dc.contributor.authorSwamy, N Ramachandra-
dc.contributor.authorJayashankara, V P-
dc.date.accessioned2010-05-14T11:43:12Z-
dc.date.available2010-05-14T11:43:12Z-
dc.date.issued2005-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8987-
dc.description823-826en_US
dc.description.abstractZinc chloride efficiently catalyzes the three-component coupling of β-keto ester, substituted aldehyde and urea or thiourea to afford the corresponding 3,4-dihydropyrimidin-2(1H)-ones/thiones respectively, the new protocol for the Biginelli reaction under microwave irradiation works in the absence of solvent, the yields are high and the reaction goes to completion within 20-35 sec.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 239/00en_US
dc.sourceIJC-B Vol.44B(04) [April 2005]en_US
dc.titleOne pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones/-thiones catalysed by zinc chloride: An improved procedure for the Biginelli reaction using microwaves under solvent free conditionen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(04) [April 2005]

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