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ChemInform Abstract: A New Route to 1,2‐Dithiole‐3‐thiones (Trithiones) by the Reaction of Enaminones with Carbon Disulfide.

Yoshinori Tominaga, Hajime Norisue, Chizuko Kamio, Toshiyuki Masunari, Yuji Miyashiro, Akíra Hosomi

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Abstract

Abstract Reaction of the cyclic enaminones (I), (VI), and (XI) with carbon disulfide (II) in the presence of a base results in cyclization to produce the fused dithiolethiones (III), (VII), and (XII).

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What this paper is about

Abstract Reaction of the cyclic enaminones (I), (VI), and (XI) with carbon disulfide (II) in the presence of a base results in cyclization to produce the fused dithiolethiones (III), (VII), and (XII).

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Available abstract

Abstract Reaction of the cyclic enaminones (I), (VI), and (XI) with carbon disulfide (II) in the presence of a base results in cyclization to produce the fused dithiolethiones (III), (VII), and (XII).

Key concepts: Chemistry, Carbon disulfide, Disulfide bond, Base (topology), Carbon fibers, Organic chemistry, Combinatorial chemistry, Medicinal chemistry

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ChemInform Abstract: A New Route to 1,2‐Dithiole‐3‐thiones (Trithiones) by the Reaction of Enaminones with Carbon Disulfide. — Research Paper | ScholarLens