Singh, Parvinder Pal and Reddy, P. Bhaskar and Sawant, Sanghapal D. and Koul, S. and Taneja, S.C. and Kumar, H.M. Sampath (2006) Domino synthesis of indenols and alkyl-indene ethers under modified Vilsmeier conditions. Tetrahedron Letters, 47 (40). pp. 7241-7243. ISSN 00404039

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Abstract

Indenols are produced in high yields through domino reactions, when electron-rich trans-stilbenes and other trans aryl–alkyl olefins were subjected to Vilsmeier formylation in the presence of excess POCl3 in a one-pot procedure. The method is even suitable for converting aryl–alkyl carbinols (precursors for olefins) directly into indenols. The corresponding indene ethers could be prepared in high yields directly when less reactive a,b-unsaturated aldehydes were subjected to cyclization in alcoholic HCl.

Item Type:	Article
Subjects:	Chemical Sciences
Divisions:	UNSPECIFIED
Depositing User:	Mr. Amit Nargotra
Date Deposited:	28 Dec 2011 08:29
Last Modified:	28 Dec 2011 08:29
URI:	http://iiim.csircentral.net/id/eprint/241

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