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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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