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ChemInform Abstract: Oxidation of Thiol with 5‐Arylidene‐1,3‐dimethylbarbituric Acid: Application to Synthesis of Unsymmetrical Disulfide.

Kei Tanaka, X. CHEN, Fumio Yoneda

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Abstract

Abstract The barbituric acid derivative (II) oxidizes the mercaptans (I) and the disulfides (III) are formed.

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What this paper is about

Abstract The barbituric acid derivative (II) oxidizes the mercaptans (I) and the disulfides (III) are formed.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

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Method / approach

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Available abstract

Abstract The barbituric acid derivative (II) oxidizes the mercaptans (I) and the disulfides (III) are formed.

Key concepts: Chemistry, Disulfide bond, Thiol, Organic chemistry, Computational chemistry, Combinatorial chemistry, Biochemistry

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ChemInform Abstract: Oxidation of Thiol with 5‐Arylidene‐1,3‐dimethylbarbituric Acid: Application to Synthesis of Unsymmetrical Disulfide. — Research Paper | ScholarLens

ChemInform Abstract: Oxidation of Thiol with 5‐Arylidene‐1,3‐dimethylbarbituric Acid: Application to Synthesis of Unsymmetrical Disulfide.

About this research paper

What this paper is about

Why it matters

Key contribution

Method / approach

Main findings

Limitations

Applications

Available abstract

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