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- W2036619367 abstract "The ant alkaloid myrmicarin 217 (1-ethyl-3,4,4a,5,6,7-hexahydro-2-propylpyrrolo[2,1,5-cd]indolizine, 1) was synthesized using a new method for the direct cyclization of appropriately disubstituted piperidines. The mechanism for the formation of the pyrrolo[2,1,5-cd]indolizine system was investigated by 1H-NMR spectroscopy, which showed the reaction to proceed through indolizidine intermediates. The course of this facile cyclization may parallel steps in the biosynthesis of mymicarin 217 and related alkaloids." @default.
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- W2036619367 date "1998-05-01" @default.
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- W2036619367 title "Synthesis of myrimcarin 217, a pyrrolo[2,1,5-cd]indolizine from ants" @default.
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- W2036619367 doi "https://doi.org/10.1016/s0040-4020(98)00223-3" @default.
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