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For some representative examples, see: indanes
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Benzo[c]fluorene:
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For some recent examples, see: Benzofurans and chromans:
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Benzo[cd]isoindolones:
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Amides are generally useful electrophiles in Parham cyclisations due to a complex induced proximity effect (CIPE). Thus, lithium-iodine exchange could be favoured first by coordination of the organolithium to the amide group, and second by stabilisation of the resulting aryllithium. For a review on CIPE, see:
-
Amides are generally useful electrophiles in Parham cyclisations due to a complex induced proximity effect (CIPE). Thus, lithium-iodine exchange could be favoured first by coordination of the organolithium to the amide group, and second by stabilisation of the resulting aryllithium. For a review on CIPE, see:. Wishler M.C., McNeil S., Snieckus V., and Beak P. Angew. Chem., Int. Ed. 43 (2004) 2206-2225
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4 reduction of the commercially available 2-chloro-3-formylquinoline. It should me mentioned that all our attempts to prepare the 3-bromomethyl-2-iodoquinoline following the procedure previously described (
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4 reduction of the commercially available 2-chloro-3-formylquinoline. It should me mentioned that all our attempts to prepare the 3-bromomethyl-2-iodoquinoline following the procedure previously described (
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33646758009
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4 reduction of the so-obtained 2-bromo-3-formylpyridine, according to literature procedures:
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69
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33646757657
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Although thieno[3, 2-f]indolizidones have been previously prepared via classical Friedel-Crafts [
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70
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] or N-acyliminium ion cyclisations [
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], our route effectively competes with these procedures, since it reduces the number of steps and gives higher global yields
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Othman M., Pigeon P., and Decroix B. Tetrahedron 54 (1998) 8737-8744 ], our route effectively competes with these procedures, since it reduces the number of steps and gives higher global yields
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Tetrahedron
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Othman, M.1
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