Article ID Journal Published Year Pages File Type
5261362 Tetrahedron Letters 2014 4 Pages PDF
Abstract
Regioselective ring-opening of the N-(2,3-epoxypropyl)phthalimide with in situ prepared dithiocarbamic acid in water is reported for the synthesis of a new family of α-phthalimido-α′-dithiocarbamato propan-2-ols. The present method is simple, EtOAc is used for work-ups and affords excellent yield of products.
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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Synthesis of α-phthalimido-α′-dithiocarbamato propan-2-ols via a one-pot, three-component epoxide ring-opening in water
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