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ChemInform Abstract: Knoevenagel Reactions of Aldehydes with Carboxy Compounds. Part 1. Reactions of p‐Nitrobenzaldehyde with Active Methine Compounds.

Makoto Tanaka, Osamu Oota, Hideo Hiramatsu, Kazuyoshi Fujiwara

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Abstract

Abstract The reaction of aldehyde (I) with acids (II) in the presence of Py (or another tert. amine) proceeds via a reversible formation of hydroxy intermediate (III) (isolable) which decarboxylates (rate determining step) to give compound (IV) (Hann and Lapworth mechanism).

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What this paper is about

Abstract The reaction of aldehyde (I) with acids (II) in the presence of Py (or another tert. amine) proceeds via a reversible formation of hydroxy intermediate (III) (isolable) which decarboxylates (rate determining step) to give compound (IV) (Hann and Lapworth mechanism).

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Available abstract

Abstract The reaction of aldehyde (I) with acids (II) in the presence of Py (or another tert. amine) proceeds via a reversible formation of hydroxy intermediate (III) (isolable) which decarboxylates (rate determining step) to give compound (IV) (Hann and Lapworth mechanism).

Key concepts: Chemistry, Knoevenagel condensation, Aldehyde, Amine gas treating, Organic chemistry, Reaction mechanism, Medicinal chemistry, Catalysis

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ChemInform Abstract: Knoevenagel Reactions of Aldehydes with Carboxy Compounds. Part 1. Reactions of p‐Nitrobenzaldehyde with Active Methine Compounds. — Research Paper | ScholarLens