Abstract
The reactivity of pyrrololactone 3 towards reductive and alkylating agents has been studied and the synthesis of diverse α, β-difunctionalised pyrroles is presented. The ambivalent reactivity of compound 3 towards the different nucleophilic reagents has been rationalised.
Keywords: pyrrole, lactone, lactol, iminium, phenylglycinol
Letters in Organic Chemistry
Title: Further Advances in the Synthesis of α,β-Difunctionalised Pyrroles
Volume: 1 Issue: 3
Author(s): Severine Hebbe and Luc Dechoux
Affiliation:
Keywords: pyrrole, lactone, lactol, iminium, phenylglycinol
Abstract: The reactivity of pyrrololactone 3 towards reductive and alkylating agents has been studied and the synthesis of diverse α, β-difunctionalised pyrroles is presented. The ambivalent reactivity of compound 3 towards the different nucleophilic reagents has been rationalised.
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Cite this article as:
Hebbe Severine and Dechoux Luc, Further Advances in the Synthesis of α,β-Difunctionalised Pyrroles, Letters in Organic Chemistry 2004; 1 (3) . https://dx.doi.org/10.2174/1570178043401027
DOI https://dx.doi.org/10.2174/1570178043401027 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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