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dc.contributor.authorRaju, B China-
dc.date.accessioned2009-01-13T05:27:54Z-
dc.date.available2009-01-13T05:27:54Z-
dc.date.issued2008-12-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/2748-
dc.description1903-1905en_US
dc.description.abstract4-Benzyloxy-3,5-dimethylphenylacetate 1 reacts with substituted benzyl amines 2a-e affords N-substituted benzyl-2-(4′-benzyloxy-3′,5′-dimethylphenyl) acetamides 3a-e, which on debenzylation give N-substituted benzyl-2-(3′,5′-dimethyl-4′-hydroxy phenyl) acetamides 4a-e in very good yields which are important intermediates for the synthesis of 1,2,3,4-tetrahydroisoquinolines.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(12) [December 2008]en_US
dc.subjectAcetamidesen_US
dc.subject4-benzyloxy-3,5-dimethylphenylacetateen_US
dc.subjectSubstituted benzyl aminesen_US
dc.subjectTetrahydroisoquinolinesen_US
dc.titleSynthesis of N-(substituted benzyl)-2-(3′,5′-dimethyl-4′-hydroxyphenyl) acetamidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(12) December 2008]

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