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ChemInform Abstract: 4‐(1,4‐Benzoquinonyl‐2)‐1,4‐dihydropyridines as Analogues of Nifedipine.

U. KUCKLAENDER, Petra Ulmer, Gabriele Zerta

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Abstract

Abstract Condensation reaction of the aldehyde (I) with the aminocyclohexenone (II) and subsequent deprotection of the phenolic hydroxy groups yield the decahydroacridinedione (III) which is oxidized with Ag2O to form the quinones (IV) or (V) depending on the amount of oxidant employed.

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What this paper is about

Abstract Condensation reaction of the aldehyde (I) with the aminocyclohexenone (II) and subsequent deprotection of the phenolic hydroxy groups yield the decahydroacridinedione (III) which is oxidized with Ag2O to form the quinones (IV) or (V) depending on the amount of oxidant employed.

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Available abstract

Abstract Condensation reaction of the aldehyde (I) with the aminocyclohexenone (II) and subsequent deprotection of the phenolic hydroxy groups yield the decahydroacridinedione (III) which is oxidized with Ag2O to form the quinones (IV) or (V) depending on the amount of oxidant employed.

Key concepts: Chemistry, Yield (engineering), Aldehyde, Nifedipine, Condensation, Condensation reaction, Medicinal chemistry, Organic chemistry

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ChemInform Abstract: 4‐(1,4‐Benzoquinonyl‐2)‐1,4‐dihydropyridines as Analogues of Nifedipine. — Research Paper | ScholarLens