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Journal of Agricultural and Food Chemistry|May 7, 2013
Highly fluorinated 2,2'-biphenols and related compounds: relationship between substitution pattern and herbicidal activityRobert Francke, Rüdiger Reingruber, Dieter Schollmeyer, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|November 25, 2017
Electrochemical Conversion of Phthaldianilides to Phthalazin-1,4-diones by Dehydrogenative N-N Bond FormationAnton Kehl, Tile Gieshoff, Dieter Schollmeyer, et al.Angewandte Chemie (International Ed. in English)|August 14, 2018
Regioselective Metal- and Reagent-Free Arylation of Benzothiophenes by Dehydrogenative ElectrosynthesisSebastian Lips, Dieter Schollmeyer, Robert Franke, et al.Acta Crystallographica. Section E, Structure Reports Online|May 17, 2012
4-[5-Amino-4-(4-fluoro-phen-yl)-3-(pyridin-4-yl)-1H-pyrazol-1-yl]benzo-nitrileBassam Abu Thaher, Pierre Koch, Dieter Schollmeyer, et al.Acta Crystallographica. Section E, Crystallographic Communications|September 24, 2015
Crystal structure of 12-benzyl-sulfanyl-2,9-di-bromo-6H-dibenzo[b,g][1,8]naphthyridin-11-oneSebastian Resch, Thomas Quell, Dieter Schollmeyer, et al.Chemical Communications (Cambridge, England)|April 14, 2010
Synthesis and molecular properties of donor-pi-spacer-acceptor ynamides with up to four conjugated alkyne unitsBernhard Witulski, Torsten Schweikert, Dieter Schollmeyer, et al.Macromolecular Rapid Communications|October 13, 2020
Racemic S-(ethylsulfonyl)-dl-cysteine N-Carboxyanhydrides Improve Chain Lengths and Monomer Conversion for β-Sheet-Controlled Ring-Opening PolymerizationTobias A Bauer, Christian Muhl, Dieter Schollmeyer, et al.Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
4-[2-(4-Fluoro-phen-yl)-1H-pyrrol-3-yl]pyridineBassam Abu Thaher, Pierre Koch, Dieter Schollmeyer, et al.Acta Crystallographica. Section E, Structure Reports Online|September 13, 2012
4-(4-Fluoro-phen-yl)-3-(pyridin-4-yl)-1-(2,4,6-trichloro-phen-yl)-1H-pyrazol-5-amineBassam Abu Thaher, Pierre Koch, Dieter Schollmeyer, et al.Journal of Colloid and Interface Science|March 15, 2011
Simple chiral urea gelators, (R)- and (S)-2-heptylurea: their gelling ability enhanced by chiralityJong-Uk Kim, Dieter Schollmeyer, Martin Brehmer, et al.Pageof 31