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Current Medicinal Chemistry|December 10, 2002
Natural product guided compound library developmentRolf Breinbauer, Michael Manger, Michael Scheck, et al.Current Opinion in Chemical Biology|May 5, 2020
Pseudo-natural products and natural product-inspired methods in chemical biology and drug discoveryMichael Grigalunas, Annina Burhop, Andreas Christoforow, et al.Angewandte Chemie (International Ed. in English)|May 2, 2018
Synthesis and In Vitro Evaluation of the Ras Farnesyltransferase Inhibitor Pepticinnamin EKlaus Hinterding, Patrizia Hagenbuch, Janos Rétey, et al.Journal of Medicinal Chemistry|August 31, 2023
Spacial Score─A Comprehensive Topological Indicator for Small-Molecule ComplexityAdrian Krzyzanowski, Axel Pahl, Michael Grigalunas, et al.The Journal of Organic Chemistry|October 29, 2008
Repulsive interaction can be a key design element of molecular rotary motorsIrina Ben Shir, Sanjita Sasmal, Tom Mejuch, et al.The ISME Journal|October 21, 2011
Potential for phosphite and phosphonate utilization by ProchlorococcusRoi Feingersch, Alon Philosof, Tom Mejuch, et al.Angewandte Chemie (International Ed. in English)|August 23, 2023
The Future of (Radio)-Labeled Compounds in Research and Development within the Life Science IndustryVolker Derdau, Charles S Elmore, Thomas Hartung, et al.Journal of the American Chemical Society|February 12, 2014
All-carbon quaternary stereogenic centers in acyclic systems through the creation of several C-C bonds per chemical stepIlan Marek, Yury Minko, Morgane Pasco, et al.Journal of Chemical Information and Modeling|October 20, 2021
Pseudonatural Products Occur Frequently in Biologically Relevant CompoundsJosé-Manuel Gally, Axel Pahl, Paul Czodrowski, et al.Angewandte Chemie (International Ed. in English)|August 11, 2011
The Pictet-Spengler reaction in nature and in organic chemistryJoachim Stöckigt, Andrey P Antonchick, Fangrui Wu, et al.Pageof 39