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- Synthesis and characterization of tris-(5-amino-8-hydroxyquinoline)aluminum complexes and their use as anode buffer layers in inverted organic solar cells. Venla M. Manninen, Walaa A. E. Omar, Juha P. Heiskanen, Helge J. Lemmetyinen, Osmo E. O. Hormi
, J. Mater. Chem.
, 2012
, 22
, 22971
- Organic chemistry
, J. Chem. Soc., Abstr.
, 1922
, 122
, i617
- Synthetic and mechanistic aspects of the regioselective base-mediated reaction of perfluoroalkyl- and perfluoroarylsilanes with heterocyclic N-oxides. David E. Stephens, Gabriel Chavez, Martin Valdes, Monica Dovalina, Hadi D. Arman, Oleg V. Larionov
, Org. Biomol. Chem.
, 2014
, 12
, 6190
- Spectroscopic study of a synthesized Alq3 end-capped oligothiophene applied in organic solar cells. Venla M. Manninen, Juha P. Heiskanen, Kimmo M. Kaunisto, Osmo E. O. Hormi, Helge J. Lemmetyinen
, RSC Adv.
, 2014
, 4
, 8846
- 88. The Skraup reaction with m-substituted anilines. L. Bradford, T. J. Elliott, F. M. Rowe
, J. Chem. Soc.
, 1947
, 437
- 116. The 5- and 8-bromination of quinoline and some of its derivatives. P. B. D. de la Mare, M. Kiamud-Din, J. H. Ridd
, J. Chem. Soc.
, 1960
, 561
- Expeditious one-pot synthesis of C3-piperazinyl-substituted quinolines: key precursors to potent c-Met inhibitors. Yuanxiang Wang, Jing Ai, Gang Liu, Meiyu Geng, Ao Zhang
, Org. Biomol. Chem.
, 2011
, 9
, 5930
- Continuous flow as an enabling technology: a fast and versatile entry to functionalized glyoxal derivatives. Fabio Lima, Mark Meisenbach, Berthold Schenkel, Joerg Sedelmeier
, Org. Biomol. Chem.
, 2021
, 19
, 2420
- Increasing saturation: development of broadly applicable photocatalytic Csp2–Csp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis. Anthony N. Cauley, Melda Sezen-Edmonds, Eric M. Simmons, Cullen L. Cavallaro
, React. Chem. Eng.
, 2021
, 6
, 1666
- Pd-catalyzed intramolecular addition of active methylene compounds to alkynes with subsequent cross-coupling with (hetero)aryl halides. Aleksandra Błocka, Paweł Woźnicki, Marek Stankevič, Wojciech Chaładaj
, RSC Adv.
, 2019
, 9
, 40152