General information
| Name: Magne |
| Surname: Sydnes |
| E-mail: magne.o.sydnes@uis.no |
| Cell phone number with international prefix: +47 47264261 |
| Country: Norway |
| Affiliation: University of Stavanger |
| Gender: F □ M X |
| Year of the PhD title: 2004 |
| Personal web page: http://www.uis.no/om-uis/kontakt-oss/finn-ansatt/sydnes-magne-olav-article74476-11198.html |
| Previous COST participation: No X Yes □ |
List of 10 selected publications within last 5 years
| 1. Magne O. Sydnes – The use of Microwave for One-pot Reductive Amination. Curr. Green Chem. 2016, 3, 101-110. |
| 2. Magne O. Sydnes, Phuc Van Le, Jens Olschimke, Peter C. Healy, Agatha Garavelas, Fatemeh M. Tajabadi, Lilianna Pedro, Ronald J. Quinn, Ian D. Jenkins – Synthesis of two chiral octahydroindole scaffolds for drug discovery. Tetrahedron 2016, 72, 1225-1228. |
| 3. Daniela M. Pampanin, Eeva K. Kemppainen, Karianne Skogland, Kåre B. Jørgensen, Magne O. Sydnes – Investigation of fixed wavelength fluorescence results for biliary metabolites of polycyclic aromatic hydrocarbons formed in Atlantic cod (Gadus morhua). Chemosphere 2016, 144, 1372-1376. |
| 4. Marianne Lorentzen, Annette Bayer, Magne O. Sydnes, Kåre B Jørgensen – Total synthesis of tubastrine and 3-dehydroxy tubastrine by microwave assisted cross-coupling reactions. Tetrahedron 2015, 71, 8278-8284. |
| 5. Magne O. Sydnes, Minoru Isobe – Exclusive formation of azo-compounds upon hydrogenolysis of nitrobenzeneseleninic acid derivatives over Pd/C. Monatsh. Chem. 2015, 146, 351-356. |
| 6. Marianne Lorentzen, Magne O. Sydnes, Kåre B. Jørgensen – Total Synthesis of (1R,2R)-1,2-Dihydrochrysene-1,2-diol. Tetrahedron 2014, 70, 9041-9051. |
| 7. Magne O. Sydnes – One-Pot Reactions: A Step Towards Greener Chemistry. Curr. Green Chem. 2014, 1, 216-226. |
| 8. Magne O. Sydnes – Use of Nanoparticles as Catalysts in Organic Synthesis – Cross-Coupling Reactions. Curr. Org. Chem. 2014, 18, 312-326. |
| 9. Sindre Å. Lunde, Magne O. Sydnes – One-Pot Procedures for the Formation of SecondaryAryl Amines from Nitro Aryls. Synlett 2013, 24, 2340-2344. |
| 10. Lena Pedersen, Mohamed F. Mady, Magne O. Sydnes – One-pot Suzuki-Miyaura cross-coupling followed by reductive monoalkylation of the resulting nitro biaryl system utilizing Pd/C as catalyst. Tetrahedron Lett. 2013, 54, 4772-4775. |
Main skills and expertise (up to 5)
| 1. Natural product synthesis |
| 2. Medicinal chemistry |
| 3. Methodology development |
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| 5. |
Main equipment/facilities available in the participants’ lab (up to 5)
| 1. 400 MHz NMR |
| 2. GC-MS |
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