Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3079
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dc.contributor.authorRamachandran, G.-
dc.date.accessioned2020-12-14T05:04:03Z-
dc.date.available2020-12-14T05:04:03Z-
dc.date.issued2014-
dc.identifier.citationChemistry Letters, 43(10), pp.1631-1633.en_US
dc.identifier.otherhttps://doi.org/10.1246/cl.140624-
dc.identifier.urihttps://www.journal.csj.jp/doi/10.1246/cl.140624-
dc.identifier.urihttp://hdl.handle.net/123456789/3079-
dc.description.abstractA highly efficient and environmentally benign protocol was developed for the synthesis of aminals using silica-supported iron(III) chloride as an active Lewis acid recyclable heterogeneous catalyst from N-nucleophiles and active carboxaldehydes. This current modest protocol is cost-effective and an environmentally benign method for the synthesis of pharmaceutically and industrially useful scaffolds.en_US
dc.language.isoenen_US
dc.publisherChemical Society of Japanen_US
dc.subjectChemoselectiveen_US
dc.subjectFeCl3en_US
dc.subjectGreen Solventen_US
dc.titleEco-efficient, Chemoselective, and Rapid Access to Aminals from Lactams Using Recyclable Silica-supported FeCl3 Catalyst in Green Solventen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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