Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3066
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, Amit-
dc.contributor.authorParella, R.-
dc.contributor.authorBabu, S.A.-
dc.date.accessioned2020-12-12T04:45:14Z-
dc.date.available2020-12-12T04:45:14Z-
dc.date.issued2014-
dc.identifier.citationSynlett, 25(6), pp. 835-842.en_US
dc.identifier.other10.1055/s-0033-1340844-
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0033-1340844-
dc.identifier.urihttp://hdl.handle.net/123456789/3066-
dc.description.abstractWe report the use of magnetic nano Fe3O4 as a mild heterogeneous catalyst for the aminolysis of epoxides with amines. The approach constitutes a green method for the formation of a variety of β-amino alcohols with very high stereo- and regioselectivity under solvent-free and ambient reaction conditions. The aminolysis of chiral epoxides with amines gave the corresponding chiral β-amino alcohols with complete inversion of stereochemistry. The magnetic nano Fe3O4 catalyst can be easily recovered and recycled.en_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.subjectAmino alcoholsen_US
dc.subjectEpoxidesen_US
dc.subjectGreen chemistryen_US
dc.subjectNano magnetiteen_US
dc.subjectRegioselectivityen_US
dc.subjectStereoselective synthesisen_US
dc.titleMagnetic Nano Fe3O4 Catalyzed Solvent-Free Stereo- and Regioselective ­Aminolysis of Epoxides by Amines; a Green Method for the Synthesis of β-Amino Alcoholsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

Files in This Item:
File Description SizeFormat 
need to add pdf....odt8.12 kBOpenDocument TextView/Open


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