Lewis-Acid-Catalysed tandem meinwald rearrangement/Intermolecular [3+2]- Cycloaddition of epoxides with Donor–acceptor cyclopropanes: Synthesis of functionalized tetrahydrofurans

dc.contributor.author	Pandey, A.K.
dc.contributor.author	Ghosh, A.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2016-11-19T06:46:43Z
dc.date.available	2016-11-19T06:46:43Z
dc.date.issued	2016-11-19
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/482
dc.description.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.	en_US
dc.language.iso	en_US	en_US
dc.subject	Asymmetric synthesis	en_US
dc.subject	Cyclization	en_US
dc.subject	Oxygen heterocycles	en_US
dc.subject	Small ring systems	en_US
dc.subject	Epoxides	en_US
dc.title	Lewis-Acid-Catalysed tandem meinwald rearrangement/Intermolecular [3+2]- Cycloaddition of epoxides with Donor–acceptor cyclopropanes: Synthesis of functionalized tetrahydrofurans	en_US
dc.type	Article	en_US