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Chemical Society Reviews|December 18, 2015
Gold catalysis in total synthesis - recent achievementsDaniel Pflästerer, A Stephen K Hashmi
The Journal of Organic Chemistry|April 19, 2012
Enantioselective total synthesis and absolute configuration of apiosporic acidMartin Gärtner, David Kossler, Daniel Pflästerer, et al.
Angewandte Chemie (International Ed. in English)|December 17, 2013
Dehydrogenative Meyer-Schuster-like rearrangement: a gold-catalyzed reaction generating an alkyneYang Yu, Weibo Yang, Daniel Pflästerer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 30, 2015
Mechanistic Insights into the Post-Cyclization Isomerization in Gold-Catalyzed 7-exo-dig-HydroarylationsDaniel Pflästerer, Sören Schumacher, Matthias Rudolph, et al.
Angewandte Chemie (International Ed. in English)|January 10, 2018
Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic EstersAdam Noble, Riccardo S Mega, Daniel Pflästerer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 30, 2014
Synthesis of highly substituted γ-butyrolactones by a gold-catalyzed cascade reaction of benzyl estersMaria Camila Blanco Jaimes, Alexander Ahrens, Daniel Pflästerer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 5, 2014
Highly diastereoselective and regioselective copper-catalyzed nitrosoformate dearomatization reaction under aerobic-oxidation conditionsWeibo Yang, Long Huang, Yang Yu, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 31, 2013
Synthesis of polycyclic indole skeletons by a gold(I)-catalyzed cascade reactionTao Wang, Shuai Shi, Daniel Pflästerer, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 29, 2014
Highly efficient gold-catalyzed synthesis of dibenzocycloheptatrienesDaniel Pflästerer, Eva Rettenmeier, Severin Schneider, et al.
Plos One|May 26, 2012
A quantitative 3D motility analysis of Trypanosoma brucei by use of digital in-line holographic microscopySebastian Weiße, Niko Heddergott, Matthias Heydt, et al.
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