2018•New Journal of ChemistryRequires access

Efficient synthetic procedure to new 2-imino-1,3-thiazolines and thiazolidin-4-ones promoted by acetonitrile electrogenerated base

Beya Haouas, Najoua Sbei, Hana Ayari, Mohamed Lamine Benkhoud, Belén Batanero

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Abstract

Regioselective sulfur–carbon bond formation from disubstituted thioureas and 1,2-dielectrophiles.

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Regioselective sulfur–carbon bond formation from disubstituted thioureas and 1,2-dielectrophiles.

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OpenAlex reports 17 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Regioselective sulfur–carbon bond formation from disubstituted thioureas and 1,2-dielectrophiles.

Key concepts: Chemistry, Acetonitrile, Regioselectivity, Base (topology), Combinatorial chemistry, Sulfur, Medicinal chemistry, Organic chemistry

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Efficient synthetic procedure to new 2-imino-1,3-thiazolines and thiazolidin-4-ones promoted by acetonitrile electrogenerated base — Research Paper | ScholarLens

Efficient synthetic procedure to new 2-imino-1,3-thiazolines and thiazolidin-4-ones promoted by acetonitrile electrogenerated base

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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