Friedel-Crafts alkylation of a cage enone: synthesis of aralkyl substituted tetracyclo[5.3.1.0([2,6]).0([4,8])]undeca-9,11-diones and the formation of fascinating novel cage compounds with pyrrole and thiophene using montmorillonite K-10

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DC Field	Value	Language
dc.contributor.author	Beena James	-
dc.contributor.author	Suresh, E	-
dc.contributor.author	Mangalam S Nair	-
dc.date.accessioned	2015-02-23T09:08:50Z	-
dc.date.available	2015-02-23T09:08:50Z	-
dc.date.issued	2007	-
dc.identifier.citation	Tetrahedron Letters 48(34):6059-6063;20 Aug 2007	en_US
dc.identifier.issn	0040-4039	-
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1797	-
dc.description.abstract	The intrinsic catalytic properties of Montmorillonite K-10 clay have been utilized for Friedel-Crafts alkylation of the polycyclic caged enone 1 using different carbo and heterocyclic aromatic systems leading to novel compounds. Carbon-carbon bond formation between the aromatic compounds and the cage system has led to three different types of products.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	Stereoselective-synthesis	en_US
dc.subject	Titanium catalysts	en_US
dc.subject	Amines	en_US
dc.subject	Reagents	en_US
dc.subject	Ketones	en_US
dc.subject	Ethers	en_US
dc.title	Friedel-Crafts alkylation of a cage enone: synthesis of aralkyl substituted tetracyclo[5.3.1.0([2,6]).0([4,8])]undeca-9,11-diones and the formation of fascinating novel cage compounds with pyrrole and thiophene using montmorillonite K-10	en_US
dc.type	Article	en_US
niist.citation		-
Appears in Collections:	2007

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