Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/482
Title: Lewis-Acid-Catalysed tandem meinwald rearrangement/Intermolecular [3+2]- Cycloaddition of epoxides with Donor–acceptor cyclopropanes: Synthesis of functionalized tetrahydrofurans
Authors: Pandey, A.K.
Ghosh, A.
Banerjee, P.
Keywords: Asymmetric synthesis
Cyclization
Oxygen heterocycles
Small ring systems
Epoxides
Issue Date: 19-Nov-2016
Abstract: A Lewis-acid-catalysed tandem Meinwald rearrangement/[3+2]-cycloaddition of epoxides with donor-acceptor cyclopropanes to synthesize varieties of cis-2,5-aryl-benzyl-substituted tetrahydrofurans is described. An enantioselective version of the same transformation was achieved using an InCl3-PyBOX catalyst system. A Lewis-acid-catalysed tandem Meinwald rearrangement/[3+2]-cycloaddition of epoxides with donor-acceptor cyclopropanes to synthesize varieties of cis-2,5-aryl-benzyl-substituted tetrahydrofurans is described. An enantioselective version of the same transformation is also presented using various BOX ligands.
URI: http://localhost:8080/xmlui/handle/123456789/482
Appears in Collections:Year-2015

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