1,4-Dipolar cycloaddition in organic synthesis: a facile route to isoquinoline fused heterocycles

Nair, Vijay ; Sreekanth, Anakkalil Ramachandran ; Abhilash, Narayana Pillai ; Biju, Akkattu Thankappan Nair ; Varma, Luxmi ; Viji, Sreemathi ; Mathew, Saumini (2005) 1,4-Dipolar cycloaddition in organic synthesis: a facile route to isoquinoline fused heterocycles ARKIVOC: Online Journal of Organic Chemistry, 2005 (11). pp. 177-188. ISSN 1424-6376

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Official URL: http://quod.lib.umich.edu/a/ark/5550190.0006.b15/1...

Abstract

The three component condensation reactions involving isoquinoline, dimethyl acetylenedicarboxylate and carbonyl dipolarophiles such o- and p-benzoquinones and N-substituted isatins constitute a one-pot synthesis of a variety of [1,3]oxazino isoquinoline derivatives via 1,4-dipolar cycloaddition.

Item Type:Article
Source:Copyright of this article belongs to Arkat-USA, Inc.
Keywords:Dimethyl Acetylenedicarboxylate; N-substituted Istain; Isoquinoline; o- and p-nenzoquinones
ID Code:84102
Deposited On:24 Feb 2012 06:09
Last Modified:24 Feb 2012 06:09

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