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Synthesis of arylacetic acid derivatives from diethyl malonate using in

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dc.contributor.author Ozdemir, I
dc.contributor.author Yigit, M
dc.contributor.author Cetinkaya, E
dc.contributor.author Cetinkaya, B
dc.date.accessioned 2022-10-19T12:12:29Z
dc.date.available 2022-10-19T12:12:29Z
dc.date.issued 2004
dc.identifier.uri http://hdl.handle.net/11616/84054
dc.description.abstract The in situ prepared three component system Pd(OAc)(2)/1,3-bis(alkyl) imidazolinium halide LHX (1-5)/Cs2CO3 catalyses the arylation of diethyl malonate efficiently with accompanying dealkoxycarbonylation. Imidazolinium salts with bulky benzyl and alkoxyethyl groups were found to be the most efficient and afforded alpha-arylacetates in high yields when employing a wide variety of substrates. (C) 2004 Elsevier Ltd. All rights reserved.
dc.description.abstract C1 Ege Univ, Dept Chem, TR-35100 Izmir, Turkey.
dc.description.abstract Inonu Univ, Dept Chem, TR-44069 Malatya, Turkey.
dc.source TETRAHEDRON LETTERS
dc.title Synthesis of arylacetic acid derivatives from diethyl malonate using in
dc.title situ formed palladium(1,3-dialkylimidazolidin-2-ylidene) catalysts


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