Ionic liquid accelerated intramolecular hetero-Diels-Alder reactions: a protocol for the synthesis of octahydroacridines

Yadav, J. S. ; Reddy, B. V. S. ; Chetia, Lakshindra ; Srinivasulu, G. ; Kunwar, A. C. (2005) Ionic liquid accelerated intramolecular hetero-Diels-Alder reactions: a protocol for the synthesis of octahydroacridines Tetrahedron Letters, 46 (6). pp. 1039-1044. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2004.11.137

Abstract

2-Azadienes derived in situ from arylamines and (R)-(+)-citronellal/3-methylcitronellal undergo intramolecular [4+2] hetero-Diels-Alder reactions in the air and moisture stable ionic liquid [bmim]BF4 in the absence of any acid catalyst to afford 1,2,3,4,4a,9,9a,10-octahydroacridine derivatives in high to quantitative yields.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Ionic Liquids (ILs); Aza-dienes; Octahydroacridines
ID Code:59596
Deposited On:07 Sep 2011 05:39
Last Modified:07 Sep 2011 05:39

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