C-10b Functionalized 5,6-dihydropyrrolo[2,1-a]isoquinolines as intermediates in the synthesis of erythrinane systems. Intra- vs. intermolecular conjugate addition based strategies

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Abstract

C-10b Functionalized 5,6-dihydropyrrolo[2,1-a]isoquinolines have been prepared via Parham cyclization and α-amidoalkylation reactions, using functionalized organolithium reagents. Their utility as intermediates in the synthesis of erythrinanes via intra or intermolecular conjugate addition reactions has been studied. Thus, a protocol for preparing the erythrinane skeleton through a Parham cyclization.intermolecular α-amidoalkylation. intermolecular conjugate addition-ring-closing metathesis process has been described. ©ARKAT USA, Inc.

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Osante, I., Abdullah, M. N., Arrasate, S., Sotomayor, N., & Lete, E. (2007). C-10b Functionalized 5,6-dihydropyrrolo[2,1-a]isoquinolines as intermediates in the synthesis of erythrinane systems. Intra- vs. intermolecular conjugate addition based strategies. Arkivoc, 2007(4), 206–219. https://doi.org/10.3998/ark.5550190.0008.418

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