|Publication type:||Article in scientific journal|
|Type of review:||Peer review (publication)|
|Title:||Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers|
Frech, Christian M.
|Published in:||Chemistry - A European Journal|
|Publisher / Ed. Institution:||Wiley|
|Subject (DDC):||540: Chemistry|
|Abstract:||Vinyl sulfides are very important synthetic intermediates in total syntheses and as precursors to a wide range of functionalized molecules. Furthermore, sulfur-containing organiccompounds commonly exhibit biological activity, and hence are frequently found in naturally occuring compounds. Moreover, these compounds have found applications in materials science, and thus are valuable synthetic targets. The increasing demand for vinyl thioethers expedited the development of new synthetic methods for these target compounds. The most attractive process for their preparation is the (100% atom efficient) alkyne hydrothiolation reaction|
|Fulltext version:||Published version|
|License (according to publishing contract):||Licence according to publishing contract|
|Departement:||Life Sciences and Facility Management|
|Appears in collections:||Publikationen Life Sciences und Facility Management|
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