Scientific article
English

Intramolecular Carbenoid Reactions of Pyrrole Derivatives: Efficient Syntheses of Pyrrolizinone and Dihydroindolizinone

Published inHelvetica chimica acta, vol. 66, no. 8, p. 2666-2671
Publication date1983-12-14
Abstract

The copper-catalyzed pyrolysis of 1-diazo-3-(pyrrol-1-yl)-2-propanone (1a) and 1-diazo-4-(pyrrol-1-yl)-2-butanone (1b) in benzene solution gave 1 H-pyrrolizin-2-(3H)-one (4a) and 5,6-dihydroindolizin-7 (8H)-one (4b), respectively, in quantitative yield. Similar pyrolysis of 1-diazo-4-(3-methylindol-1-yl)-2-butanone (9) was less efficient giving 1-methylbenzo[b]-5,6-dihydroindroindolizin-7 (8H)-one (10) and 4-(3-methylindol-1-yl)-but-1-en-3-one (11) in 7% and 24% yield, respectively.

Citation (ISO format)
JEFFORD, Charles, JOHNCOCK, William. Intramolecular Carbenoid Reactions of Pyrrole Derivatives: Efficient Syntheses of Pyrrolizinone and Dihydroindolizinone. In: Helvetica chimica acta, 1983, vol. 66, n° 8, p. 2666–2671. doi: 10.1002/hlca.19830660835
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Journal ISSN0018-019X
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