A highly efficient green synthesis of 1, 8-dioxo-octahydroxanthenes

<p>Abstract</p> <p>SmCl<sub>3 </sub>(20 mol%) has been used as an efficient catalyst for reaction between aromatic aldehydes and 5,5-dimethyl-1,3-cyclohexanedione at 120°C to give 1,8-dioxo-octahydroxanthene derivatives in high yield. The same reaction in water, at room...

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Bibliographic Details
Main Authors: Ilangovan Andivelu, Malayappasamy Subramani, Muralidharan Samraj, Maruthamuthu Sundaram
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Chemistry Central Journal
Online Access:http://journal.chemistrycentral.com/content/5/1/81
Description
Summary:<p>Abstract</p> <p>SmCl<sub>3 </sub>(20 mol%) has been used as an efficient catalyst for reaction between aromatic aldehydes and 5,5-dimethyl-1,3-cyclohexanedione at 120°C to give 1,8-dioxo-octahydroxanthene derivatives in high yield. The same reaction in water, at room temperature gave only the open chain analogue of 1,8-dioxo-octahydroxanthene. Use of eco-friendly green Lewis acid, readily available catalyst and easy isolation of the product makes this a convenient method for the synthesis of either of the products.</p>
ISSN:1752-153X