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Beilstein Journal of Organic Chemistry|February 25, 2026
Ring contraction and ring expansion reactions in terpenoid biosynthesis and their application to total synthesisNicolas Kratena, Nicolas Heinzig, Peter GärtnerDrug Testing and Analysis|February 7, 2022
Implementation of a marker substance for monitoring in situ 17-keto modifications in endogenous steroids caused by microbiological contaminationSandra Pfeffer, Günter Gmeiner, Peter GärtnerSteroids|January 6, 2005
First synthesis of a pentadeuterated 3'-hydroxystanozolol--an internal standard in doping analysisWolfgang Felzmann, Günter Gmeiner, Peter GärtnerOrganic & Biomolecular Chemistry|July 27, 2023
A biomimetic approach for the concise total synthesis of greenwaylactams A-CNicolas Kratena, Matthias Weil, Peter GärtnerOrganic Chemistry Frontiers : an International Journal of Organic Chemistry|March 20, 2026
Design principles for enantiospecific para- and ortho-[3,3] rearrangements of chiral aryl-allyl ethersJohanna Breinsperger, Maximilian Kaiser, Peter GärtnerActa Crystallographica. Section E, Crystallographic Communications|March 13, 2023
Crystal structures of two 1,2,3,4-tetra-hydro-naphthalenes obtained during efforts towards the total synthesis of elisabethin AMaximilian Kaiser, Matthias Weil, Peter Gärtner, et al.Steroids|August 25, 2016
Synthesis of 17β-hydroxymethyl-17α-methyl-18-norandrosta-1,4,13-trien-3-one: A long-term metandienone metaboliteNicolas Kratena, Valentin S Enev, Günter Gmeiner, et al.Steroids|February 20, 2022
Detection of DHCMT long-term metabolite glucuronides with LC-MSMS as an alternative approach to conventional GC-MSMS analysisLorenz Göschl, Günter Gmeiner, Peter Gärtner, et al.Journal of Mass Spectrometry : JMS|June 26, 2008
Synthesis and identification of hydroxylated metabolites of the anti-estrogenic agent cyclofenilPeter Gärtner, Karin Hofbauer, Christian Reichel, et al.Steroids|August 30, 2020
Synthesis of human long-term metabolites of dehydrochloromethyltestosterone and oxymesteroneNicolas Kratena, Sandra Pfeffer, Valentin S Enev, et al.Pageof 2