Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/466
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRaju, B China-
dc.contributor.authorNeelakantan, Parvathi-
dc.contributor.authorBhalerao, U T-
dc.date.accessioned2008-03-24T10:57:59Z-
dc.date.available2008-03-24T10:57:59Z-
dc.date.issued2007-01-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/466-
dc.description201-203en_US
dc.description.abstractReaction of 4-benzyloxy-3,5-dimethyl benzyl bromide 4 and N-tosyl-3,4-dimethoxy benzyl amine 5 gives the N-(4′-benzyloxy-3′,5′-dimethylbenzyl)-N-tosyl-3,4-dimethoxybenzyl amine 6. The obtained product on debenzylation affords N-(3′,5′-dimethyl-4′-hydroxybenzyl)-N-tosyl-3,4-dimethoxybenzyl amine 7 in 94% yield, which is key intermediate in the synthesis of isoindolines.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.⁸ C07Cen_US
dc.sourceIJCB Vol.46B(1) [January 2007]en_US
dc.subjectN-(3′,5′-dimethyl-4′-hydroxybenzyl)-N-tosyl-3,4-di¬¬¬me¬thoxybenzyl amineen_US
dc.subjectIsoindolinesen_US
dc.titleSynthesis of N-(3′,5′-dimethyl- 4′-hydroxybenzyl)- N-tosyl-3,4-dimethoxybenzyl amineen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(01) [January 2007]

Files in This Item:
File Description SizeFormat 
IJCB 46B(1) (2007) 201-203.pdf131.4 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.