Stereocontrolled Conversion of 3,5-Dioxopyrrolizidine Into (Z)- and (E)- 5-Acetonylpyrrolizidin-3-ones
- 1 March 1989
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (5-6) , 835-841
- https://doi.org/10.1080/00397918908051001
Abstract
Stereocontrolled synthesis of (Z)-5-acetonyl-pyrrolizidin-3-one (4) and (E)-isomer 5 from 3,5-dioxopyrrolizidine 1 is described.Keywords
This publication has 8 references indexed in Scilit:
- Recent Advances in the Synthesis of PyrrolizidinesHETEROCYCLES, 1988
- Amnesia-reversal activity of a series of cyclic imidesJournal of Medicinal Chemistry, 1987
- Pyrrolizine ChemistrySynthesis, 1987
- (E)-5-Hydroxypyrrolizidin-3-one: versatile synthon for the synthesis of 5-substituted 2-pyrrolidones and (Z)-3-alkylpyrrolizidinesThe Journal of Organic Chemistry, 1982
- (5Z,8E)-3-Heptyl-5-methylpyrrolizidine from a thief antThe Journal of Organic Chemistry, 1980
- Synthesis of anatoxin a via intramolecular cyclization of iminium saltsJournal of the American Chemical Society, 1979
- Anatoxin-a, a toxic alkaloid from Anabaena flos-aquae NRC-44hCanadian Journal of Chemistry, 1977
- Sur les acides aminodicarboxyliques symétriques et leur cyclisationCollection of Czechoslovak Chemical Communications, 1947