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(a) Mamane, V.; Ledoux-Rak, I.; Deveau, S.; Zyss, J.; Riant, O. Synthesis 2003, 455-467.
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12
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25444525308
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note
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The nomenclature is given by analogy with the one used for benzoquinoline and -isoquinoline.
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14
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7044241256
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19
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21
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25444432969
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note
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Compounds 6, 17, (R)-17, and 24 are very unstable and were cyclized directly after the deprotection step.
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23
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4644245555
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For a recent review see: Espinet, P.; Echavarren, A. M. Angew. Chem., Int. Ed. 2004, 43, 4704-4734.
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0021143098
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29
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25444433490
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note
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One diastereoisomer has been isolated by chromatography on silica gel and characterized.
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30
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85050443859
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The stereochemistry is given according to the Schlögl rule: Schlögl, K. Top. Stereochem. 1967, 1, 39-93.
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