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  4. <i>Michael</i> Reactions of α-Unsubstituted Trisubstituted 1/<i>H</i>-Pyrroles
 
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<i>Michael</i> Reactions of α-Unsubstituted Trisubstituted 1/<i>H</i>-Pyrroles

Auteur(s)
Lüönd Rainer
Neier, Reinhard 
Institut de chimie 
Date de parution
1991
In
Helvetica Chimica Acta, Wiley, 1991/74/1/91-102
Résumé
To obtain stable derivatives of α-unsubstituted pyrroles, the reaction of the test pyrrole <b>9</b> with a series of chalcones <b>14a-h</b> were studied. Michael adducts <b>16b-h</b> could be isolated. In order to synthesize coloured derivatives, the reaction of different pyrroles <b>9</b>, <b>2</b>1, <b>23</b>, and <b>25</b> with diphenylpropynone <b>19</b> was investigated. In these cases, too, <b>Michael</b>-addition products were formed. The intense absorption band around 400 nm makes the identification of these derivatives easy.
Identifiants
https://libra.unine.ch/handle/123456789/17674
Type de publication
journal article
Dossier(s) à télécharger
 main article: L_nd_Rainer_-_Michael_Reactions_ofa-Unsubstituted_Trisubstituted_20070822.pdf (796.29 KB)
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