Abstract
Formylation of 1-phenylpyrrole gave mainly the 2-aldehyde which was converted to the methyl ester. Chlorination produced the 4- and 5-monochloro, the 4,5-dichloro and the 3,4,5-trichloro derivatives and 2-methoxycarbonyl-5-oxo-1-phenyl-2,3,4-trichloro-3-pyrroline which were identified spectroscopically. The mass spectral cracking patterns of the chloropyrrole esters have been interpreted.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
13 articles.
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