Abstract
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under more vigorous conditions, pyrroles are formed as thermodynamically controlled products by way of a 1,3- hydride shift.
Keywords: enamine, pyrrole, isomerization, pyrroline
Letters in Organic Chemistry
Title: Synthesis and Isomerization of 3-Pyrroline Enamines
Volume: 1 Issue: 1
Author(s): A. Gilbert Cook, Karen A. Switek, Kenneth A. Cutler and Allison M. Witt
Affiliation:
Keywords: enamine, pyrrole, isomerization, pyrroline
Abstract: 3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under more vigorous conditions, pyrroles are formed as thermodynamically controlled products by way of a 1,3- hydride shift.
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Cite this article as:
Cook Gilbert A., Switek A. Karen, Cutler A. Kenneth and Witt M. Allison, Synthesis and Isomerization of 3-Pyrroline Enamines, Letters in Organic Chemistry 2004; 1 (1) . https://dx.doi.org/10.2174/1570178043488734
DOI https://dx.doi.org/10.2174/1570178043488734 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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