Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Gerber, Roman | - |
| dc.contributor.author | Frech, Christian M. | - |
| dc.date.accessioned | 2018-08-24T14:12:08Z | - |
| dc.date.available | 2018-08-24T14:12:08Z | - |
| dc.date.issued | 2012 | - |
| dc.identifier.issn | 0947-6539 | de_CH |
| dc.identifier.issn | 1521-3765 | de_CH |
| dc.identifier.uri | https://digitalcollection.zhaw.ch/handle/11475/9649 | - |
| dc.description.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 | de_CH |
| dc.language.iso | en | de_CH |
| dc.publisher | Wiley | de_CH |
| dc.relation.ispartof | Chemistry - A European Journal | de_CH |
| dc.rights | Licence according to publishing contract | de_CH |
| dc.subject.ddc | 540: Chemie | de_CH |
| dc.title | Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium : selective formation of cis-configured vinyl thioethers | de_CH |
| dc.type | Beitrag in wissenschaftlicher Zeitschrift | de_CH |
| dcterms.type | Text | de_CH |
| zhaw.departement | Life Sciences und Facility Management | de_CH |
| dc.identifier.doi | 10.1002/chem.201200388 | de_CH |
| dc.identifier.pmid | 22700478 | de_CH |
| zhaw.funding.eu | No | de_CH |
| zhaw.issue | 29 | de_CH |
| zhaw.originated.zhaw | No | de_CH |
| zhaw.pages.end | 8905 | de_CH |
| zhaw.pages.start | 8901 | de_CH |
| zhaw.publication.status | publishedVersion | de_CH |
| zhaw.volume | 18 | de_CH |
| zhaw.publication.review | Peer review (Publikation) | de_CH |
| 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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