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ChemInform Abstract: A Convenient One‐Pot Synthesis of 3‐Thio‐Substituted Coumarins.

V. K. AHLUWALIA, Mohammad Alauddin, Chandra Has Khanduri, V. D. MEHTA

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Abstract

Abstract Alkylation of the heterocyclic thiols (I) with chloroacetonitrile (II) yields the cyanomethyl sulfides (III) which undergo ring closure with the o‐hydroxybenzaldehydes (IV), forming the coumarinimines (V).

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What this paper is about

Abstract Alkylation of the heterocyclic thiols (I) with chloroacetonitrile (II) yields the cyanomethyl sulfides (III) which undergo ring closure with the o‐hydroxybenzaldehydes (IV), forming the coumarinimines (V).

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Available abstract

Abstract Alkylation of the heterocyclic thiols (I) with chloroacetonitrile (II) yields the cyanomethyl sulfides (III) which undergo ring closure with the o‐hydroxybenzaldehydes (IV), forming the coumarinimines (V).

Key concepts: Chemistry, Thio-, Ring (chemistry), Alkylation, Closure (psychology), Medicinal chemistry, Combinatorial chemistry, Organic chemistry

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ChemInform Abstract: A Convenient One‐Pot Synthesis of 3‐Thio‐Substituted Coumarins. — Research Paper | ScholarLens