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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 21, 1991 - Issue 18-19
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Original Articles

Tetramethylammonium Glycinate: A New Reagent for Improved Pyrrole Synthesis by [3+2] Cyclization

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Pages 1971-1979 | Received 20 May 1991, Published online: 23 Sep 2006
 

Abstract

The novel reagent tetramethylammonium glycinate has been introduced as the most effective glycine derivative for the convenient synthesis of 4, 5, 6, 7-tetrahydroisoindoles (orpyrroles unsubstituted in the 2 and 5 positions) from 1,3-dicarbonyl compounds by [3+2] cyclization. The reaction has been shown to be catalyzed by 2,6-di(tert.buty1) pyridine reagents to triple the reported yield.

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