1986
DOI: 10.1039/c39860000576
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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 ?,4-dihalogenobut-2-enes, affords vicinal thiocyanatoisothiocyanates, which are trapped to give thiazolidinones or dihydrothiazoies, or indirectly aminothiols.

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