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- W1520727610 endingPage "123" @default.
- W1520727610 startingPage "15" @default.
- W1520727610 abstract "This chapter provides an overview of dithioacetals and their direct chemical transformations. Dithioacetals and their derivatives comprise the largest recorded class of acyclic carbohydrate derivatives. They are versatile intermediates in synthesis not only because a multitude of transformations are possible at the dithioacetal group, but also because all of the hydroxyl groups of the sugar chain are available for chemical transformation or selective protection. Of particular importance is the fact that they provide a route for kinetically controlled ring-closure of the sugar under neutral conditions by the action of mercury (II) salts, thus providing a useful route of access to furanosides. Although dithioacetals are odorless, an inherent practical disadvantage of their preparation is the generally disagreeable scent of the lower thiols. Furthermore, appended to this chapter is a set of tables that lists the melting points and specific rotations of sugar dithioacetals and certain derivatives." @default.
- W1520727610 created "2016-06-24" @default.
- W1520727610 creator A5027165475 @default.
- W1520727610 creator A5067132812 @default.
- W1520727610 date "1976-01-01" @default.
- W1520727610 modified "2023-10-03" @default.
- W1520727610 title "Dithioacetals of Sugars" @default.
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