ChemInform Abstract: N‐(1,3‐Thiazol‐5(4H)‐ylidene)amines via 1,3‐Dipolar Cycloaddition of Azides and 1,3‐Thiazole‐5(4H)‐thiones.

Pekcan, S.; Heimgartner, Heinz

doi:10.1002/chin.198906161

ChemInform

1989

DOI: 10.1002/chin.198906161

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ChemInform Abstract: N‐(1,3‐Thiazol‐5(4H)‐ylidene)amines via 1,3‐Dipolar Cycloaddition of Azides and 1,3‐Thiazole‐5(4H)‐thiones.

S. Pekcan¹,

Heinz Heimgartner²

Abstract: ChemInform Abstract Organic azides (II) react with the thiazolethiones (I) in toluene at 90 rc C to give the thiazolimines (III). A reaction mechanism for the formation of these scarcely investigated thiazole derivatives is discussed in detail.

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ChemInform Abstract: N‐(1,3‐Thiazol‐5(4H)‐ylidene)amines via 1,3‐Dipolar Cycloaddition of Azides and 1,3‐Thiazole‐5(4H)‐thiones.

Abstract: ChemInform Abstract Organic azides (II) react with the thiazolethiones (I) in toluene at 90 rc C to give the thiazolimines (III). A reaction mechanism for the formation of these scarcely investigated thiazole derivatives is discussed in detail.

Cited by 0 publications

References 1 publication

No citations

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