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Michael Reactions of α‐Unsubstituted Trisubstituted 1 H ‐Pyrroles
Author(s) -
Lüönd Rainer,
Neier Reinhard
Publication year - 1991
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19910740111
Subject(s) - chemistry , michael reaction , pyrrole , adduct , organic chemistry , medicinal chemistry , catalysis
To obtain stable derivatives of α‐unsubstituted pyrroles, the reaction of the test pyrrole 9 with a series of chalcones 14a – h were studied. Michael adducts 16b – h could be isolated. In order to synthesize coloured derivatives, the reaction of different pyrroles 9, 21, 23 , and 25 with diphenylpropynone 19 was investigated. In these cases, too, Michael ‐addition products were formed. The intense absorption band around 400 nm makes the identification of these derivatives easy.

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