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
Authors: Gerber, Roman
Frech, Christian M.
DOI: 10.1002/chem.201200388
Published in: Chemistry - A European Journal
Volume(Issue): 18
Issue: 29
Pages: 8901
Pages to: 8905
Issue Date: 2012
Publisher / Ed. Institution: Wiley
ISSN: 0947-6539
Language: English
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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