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 |
Page(s): | 8901 |
Pages to: | 8905 |
Issue Date: | 2012 |
Publisher / Ed. Institution: | Wiley |
ISSN: | 0947-6539 1521-3765 |
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 |
URI: | https://digitalcollection.zhaw.ch/handle/11475/9649 |
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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Gerber, R., & Frech, C. M. (2012). Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers. Chemistry - A European Journal, 18(29), 8901–8905. https://doi.org/10.1002/chem.201200388
Gerber, R. and Frech, C.M. (2012) ‘Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers’, Chemistry - A European Journal, 18(29), pp. 8901–8905. Available at: https://doi.org/10.1002/chem.201200388.
R. Gerber and C. M. Frech, “Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers,” Chemistry - A European Journal, vol. 18, no. 29, pp. 8901–8905, 2012, doi: 10.1002/chem.201200388.
GERBER, Roman und Christian M. FRECH, 2012. Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers. Chemistry - A European Journal. 2012. Bd. 18, Nr. 29, S. 8901–8905. DOI 10.1002/chem.201200388
Gerber, Roman, and Christian M. Frech. 2012. “Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium : Selective Formation of Cis-Configured Vinyl Thioethers.” Chemistry - A European Journal 18 (29): 8901–5. https://doi.org/10.1002/chem.201200388.
Gerber, Roman, and Christian M. Frech. “Alkyne Hydrothiolation Catalyzed by a Dichlorobis(aminophosphine) Complex of Palladium : Selective Formation of Cis-Configured Vinyl Thioethers.” Chemistry - A European Journal, vol. 18, no. 29, 2012, pp. 8901–5, https://doi.org/10.1002/chem.201200388.
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