Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Anders Kadziola"'
Autor:
Martin Drøhse Kilde, Adrian H. Murray, Cecilie Lindholm Andersen, Freja Eilsø Storm, Katrin Schmidt, Anders Kadziola, Kurt V. Mikkelsen, Frank Hampel, Ole Hammerich, Rik R. Tykwinski, Mogens Brøndsted Nielsen
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
6,6,12-graphyne is an intriguing synthetic allotrope of carbon that is predicted to have unique electronic properties but has not been successfully synthesized. Here, the authors prepare a series of radiaannulene oligomers that can be regarded as lar
Externí odkaz:
https://doaj.org/article/692d0972c3a646db833e134adb200408
Publikováno v:
Catalysts, Vol 10, Iss 12, p 1481 (2020)
Carbon dioxide is an intrinsically stable molecule; however, it can readily react with various nucleophilic reagents. In the presence of a cyanide source, CO2 was proven to be useful to promote addition reactions. Here we report the use of CO2 to fac
Externí odkaz:
https://doaj.org/article/4cc7260230624488bf3d188cd5e6a856
Autor:
Huixin Jiang, Virginia Mazzanti, Christian R. Parker, Søren Lindbæk Broman, Jens Heide Wallberg, Karol Lušpai, Adam Brincko, Henrik G. Kjaergaard, Anders Kadziola, Peter Rapta, Ole Hammerich, Mogens Brøndsted Nielsen
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 930-948 (2015)
A selection of cyclic and acyclic acetylenic scaffolds bearing two tetrathiafulvalene (TTF) units was prepared by different metal-catalyzed coupling reactions. The bridge separating the two TTF units was systematically changed from linearly conjugate
Externí odkaz:
https://doaj.org/article/34bf1d584bd64413b3fcac906b59f4eb
Autor:
Søren Lindbæk Broman, Sophie Lehn Brand, Christian Richard Parker, Michael Åxman Petersen, Christian Gregers Tortzen, Anders Kadziola, Kristine Kilså, Mogens Brøndsted Nielsen
Publikováno v:
ARKIVOC, Vol 2011, Iss 9, Pp 51-67 (2011)
Externí odkaz:
https://doaj.org/article/b25ba1a943ba4e42b871f82e13983123
Autor:
Mogens Nielsen, Anders Kadziola, Andreas Erbs Hillers-Bendtsen, Kurt V. Mikkelsen, Viktor Bliksted Roug Pedersen, Jeppe Granhøj
Publikováno v:
Chemistry – A European Journal. 27:8315-8324
Polycyclic aromatic hydrocarbons (PAHs) have found strong interest for their electronic properties and as model systems for graphene. While PAHs have been studied intensively as single units, here PAHs were constructed in ladder-type arrangements usi
Publikováno v:
Journal of Sulfur Chemistry. 41:357-368
Thieno-fused subporphyrazines (TPs) containing a central and axially substituted boron atom are a class of compounds with interesting optical and redox properties. Here we present our efforts towards expanding this class of compounds using various th
Autor:
Mu-Hyun Baik, Ji-Woong Lee, Anders Kadziola, Gyumin Kang, Myungjo J. Kim, Yang Yang, Xinyi Ren, Hee-Yoon Lee, Tamal Roy, Suyeon Kim
Publikováno v:
Roy, T, Kim, M J, Yang, Y, Kim, S, Kang, G, Ren, X, Kadziola, A, Lee, H-Y, Baik, M-H & Lee, J-W 2019, ' Carbon Dioxide-Catalyzed Stereoselective Cyanation Reaction ', ACS Catalysis, vol. 9, no. 7, pp. 6006-6011 . https://doi.org/10.1021/acscatal.9b01087
We report a Michael-type cyanation reaction of coumarins by using CO2 as a catalyst. The delivery of the nucleophilic cyanide was realized by catalytic amounts of CO2, which forms cyanoformate and ...
Autor:
Martyn Jevric, Anders Kadziola, Kurt V. Mikkelsen, Mogens Brøndsted Nielsen, Lotte Metz, Oliver Christensen, Martin Drøhse Kilde, Martin Abildgaard, Josefine Mogensen
Publikováno v:
European Journal of Organic Chemistry. 2019:1986-1993
Autor:
Marco Santella, Henrik Gotfredsen, Mogens Brøndsted Nielsen, Anders Kadziola, Martin Drøhse Kilde
Publikováno v:
Molecular Systems Design & Engineering. 4:199-205
One convenient way of reversibly modulating the emission properties of a fluorophore is by introducing a photochromic unit that upon irradiation is converted into an isomeric unit that can quench the fluorescence of the fluorophore. Here we present t
Publikováno v:
Dotzauer, S, Hadaf, G B, Kamounah, F S, Kadziola, A & Lee, J W 2020, ' A CO 2-mediated conjugate cyanide addition to chalcones ', Catalysts, vol. 10, no. 12, 1481, pp. 1-9 . https://doi.org/10.3390/catal10121481
Catalysts, Vol 10, Iss 1481, p 1481 (2020)
Catalysts, Vol 10, Iss 1481, p 1481 (2020)
Carbon dioxide is an intrinsically stable molecule; however, it can readily react with various nucleophilic reagents. In the presence of a cyanide source, CO2 was proven to be useful to promote addition reactions. Here we report the use of CO2 to fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cae6fd61cea4cf5194d4d72309229b9
https://curis.ku.dk/ws/files/258328676/catalysts_10_01481_v2.pdf
https://curis.ku.dk/ws/files/258328676/catalysts_10_01481_v2.pdf