Issue 7, 1986

Synthetic procedures via rearrangement of 1,4-dithiocyanatobut-2-enes

Abstract

Thermal rearrangement of 1,4-dithiocyanatobut-2-enes, available by either thiocyanogenation of 1,3-dienes or from 1,4-dihalogenobut-2-enes, affords vicinal thiocanatoisothiocyanates, which are trapped to give thiazolidinones or dihydrothiazoles, or indirectly aminothiols.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 576-577

Synthetic procedures via rearrangement of 1,4-dithiocyanatobut-2-enes

E. H. M. A. Elall and J. M. Mellor, J. Chem. Soc., Chem. Commun., 1986, 576 DOI: 10.1039/C39860000576

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