| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220065 | Tetrahedron | 2012 | 6 Pages |
Abstract
The synthesis of anomeric thiocyanates with the α- and β-configuration is described. Reactions performed under standard conditions afforded the 1,2-trans derivatives as the main products, whereas in the presence of the quaternary ammonium salts, the 1,2-cis-thiocyanates were formed preferentially. The strong influence of the bromide ions on the distribution of the products is discussed.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Piotr Cmoch, Zbigniew Pakulski,