Synthesis of symmetrical and unsymmetrical trisubstituted benzene derivatives through ring-closing alkyne metathesis strategy and depropargylation with various catalysts

Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/5456

Title:	Synthesis of symmetrical and unsymmetrical trisubstituted benzene derivatives through ring-closing alkyne metathesis strategy and depropargylation with various catalysts
Authors:	KOTHA, S BANSAL, D KUMAR, RV
Keywords:	cycloaddition reaction olefin-metathesis nobel lecture trimerization cyclotrimerization cascade complexes molecules route
Issue Date:	2009
Publisher:	COUNCIL SCIENTIFIC & INDUSTRIAL RES
Citation:	INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 48(2), 225-230
Abstract:	Alkyne trimerization by application of the Grubbs ruthenium first generation catalyst has been demonstrated. In this regard, triaryloxymethylbenzene derivatives have been generated by cotrimerization of propargylated phenol derivatives with the aid of the Grubbs catalyst. Depropargylation under various catalysts have been studied.
URI:	http://dspace.library.iitb.ac.in/xmlui/handle/10054/5456 http://hdl.handle.net/10054/5456
ISSN:	0376-4699
Appears in Collections:	Article

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