Synthesis of 5,8-dimethoxy-2(1H)-quinoli
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Ferrer, Pedro ;Avendaño, Carmen ;Söllhuber, Mónica
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Article
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1995
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John Wiley and Sons
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English
⚖ 444 KB
## Abstract The title compounds 12, which are key intermediates for antitumoral diazaquinomycin A analogues, are obtained by intramolecular Wittig reaction of 1‐[3′,6′‐dimethoxy‐2′‐(α‐oxoacylamino)phenyl]alkyltriphenylphosphonium salts 11, which are prepared via lithiation of 2′,5′‐dimethoxy‐__N__‐