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Organic Letters|February 19, 2019
Total Synthesis of (-)-Oxycodone via Anodic Aryl-Aryl CouplingAlexander Lipp, Maximilian Selt, Dorota Ferenc, et al.
Beilstein Journal of Organic Chemistry|February 2, 2017
Characterization of the synthetic cannabinoid MDMB-CHMCZCACarina Weber, Stefan Pusch, Dieter Schollmeyer, et al.
Acta Crystallographica. Section E, Structure Reports Online|September 13, 2012
(2E,4R,5R,6S)-2-(4,5,6-Trihy-droxy-cyclo-hex-2-en-1-yl-idene)acetonitrileAlphonsine N Guedem, Louis P Sandjo, Till Opatz, et al.
Journal of the American Chemical Society|October 8, 2019
Dibenzo[hi,st]ovalene as Highly Luminescent Nanographene: Efficient Synthesis via Photochemical Cyclodehydroiodination, Optoelectronic Properties, and Single-Molecule SpectroscopyQiang Chen, Stefan Thoms, Sven Stöttinger, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
catena-Poly[[aqua-sodium(I)]-μ-[2,2'-(disulfanedi-yl)bis-(pyridine N-oxide)]-μ-(pyridine-2-thiol-ato 1-oxide)]B Ravindran Durai Nayagam, Samuel Robinson Jebas, J Jebaraj Devadasan, et al.
The Journal of Organic Chemistry|July 1, 2017
Mixed Phenyl and Thiophene Oligomers for Bridging Nitronyl NitroxidesKubandiran Kolanji, Prince Ravat, Artem S Bogomyakov, et al.
Chemistryopen|June 17, 2016
Solvent-Dependent Facile Synthesis of Diaryl Selenides and Biphenols Employing Selenium DioxideThomas Quell, Michael Mirion, Dieter Schollmeyer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 15, 2019
Selective Formation of 4,4'-Biphenols by Anodic Dehydrogenative Cross- and Homo-Coupling ReactionBenedikt Dahms, Philipp J Kohlpaintner, Anton Wiebe, et al.
Organic Letters|October 24, 2018
Electrochemical Formation of 3,5-Diimido-1,2-dithiolanes by Dehydrogenative CouplingValentina M Breising, Tile Gieshoff, Anton Kehl, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 21, 2015
Source of Selectivity in Oxidative Cross-Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3-Hexafluoropropan-2-olBernd Elsler, Anton Wiebe, Dieter Schollmeyer, et al.
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