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

Nair, Vijay ; Ramachandran, Sreekanth ; Abhilash, Narayana ; Biju, Akkattu ; 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. 178-188. ISSN 1424-6376

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Official URL: http://dx.doi.org/10.3998/ark.5550190.0006.b15

Abstract

The three component condensation reactions involving isoquinoline, dimethyl acetylenedicarboxylate and carbonyl dipolarophiles such as 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 isatins, isoquinoline, o- and p-benzoquinones
ID Code:128757
Deposited On:03 Nov 2022 06:58
Last Modified:11 Nov 2022 04:08

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