Facile Synthesis of the Isoquinoline Alkaloids Doryanine and Oxyhydrastinine

Abstract Starting from 4,5-(methylenedioxy)homophthalic acid, a concise and efficient synthesis of the isoquinoline alkaloids doryanine and oxyhydrastinine is described via the corresponding homophthalimide utilizing a one-pot regioselective reductive dehydration and catalytic hydrogenation pathway.

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Veröffentlicht in:Synthesis (Stuttgart) 2014, Vol.46 (14), p.1954-1956
Hauptverfasser: Jangir, Ravi, Gadre, Smita R., Argade, Narshinha P.
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract Starting from 4,5-(methylenedioxy)homophthalic acid, a concise and efficient synthesis of the isoquinoline alkaloids doryanine and oxyhydrastinine is described via the corresponding homophthalimide utilizing a one-pot regioselective reductive dehydration and catalytic hydrogenation pathway.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0033-1341158