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Chemical Communications (Cambridge, England)|January 22, 2014
Catalytic metal-free Si-N cross-dehydrocouplingLutz Greb, Sergej Tamke, Jan ParadiesChemistry (Weinheim an Der Bergstrasse, Germany)|April 17, 2015
Autoinduced catalysis and inverse equilibrium isotope effect in the frustrated Lewis pair catalyzed hydrogenation of iminesSebastian Tussing, Lutz Greb, Sergej Tamke, et al.Organic & Biomolecular Chemistry|October 9, 2014
Frustrated Lewis pair catalyzed hydrosilylation and hydrosilane mediated hydrogenation of fulvenesSergej Tamke, Constantin-G Daniliuc, Jan ParadiesTopics in Current Chemistry|November 1, 2012
Paracyclophane derivatives in frustrated Lewis pair chemistryLutz Greb, Jan ParadiesAngewandte Chemie (International Ed. in English)|March 4, 2016
Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation SequenceSergej Tamke, Zheng-Wang Qu, Nikolai A Sitte, et al.Dalton Transactions (Cambridge, England : 2003)|April 19, 2012
[2.2]Paracyclophane derived bisphosphines for the activation of hydrogen by FLPs: application in domino hydrosilylation/hydrogenation of enonesLutz Greb, Pascual Oña-Burgos, Adam Kubas, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|June 27, 2018
Lewis Superacids: Classifications, Candidates, and ApplicationsLutz GrebEuropean Journal of Inorganic Chemistry|August 1, 2022
Valence Tautomerism of p-Block Element Compounds - An Eligible Phenomenon for Main Group Catalysis?Lutz GrebAngewandte Chemie (International Ed. in English)|January 12, 2022
Calix[4]pyrrolato Stannate(II): A Tetraamido Tin(II) Dianion and Strong Metal-Centered σ-DonorHeiko Ruppert, Lutz GrebAngewandte Chemie (International Ed. in English)|November 10, 2021
What Distinguishes the Strength and the Effect of a Lewis Acid: Analysis of the Gutmann-Beckett MethodPhilipp Erdmann, Lutz GrebPageof 12