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Chemical Communications (Cambridge, England)|February 14, 2024
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletonsKimia Aghaie, Kamran Amiri, Mohammad Rezaei-Gohar, et al.
ACS Medicinal Chemistry Letters|October 24, 2017
Lucky Switcheroo: Dramatic Potency and Selectivity Improvement of Imidazoline Inhibitors of Human Carbonic Anhydrase VIIStanislav Kalinin, Stanislav Kopylov, Tiziano Tuccinardi, et al.
European Journal of Medicinal Chemistry|March 29, 2024
Discovery and characterization of potent spiro-isoxazole-based cereblon ligands with a novel binding modeRobert Shevalev, Luca Bischof, Alexander Sapegin, et al.
Bioorganic & Medicinal Chemistry Letters|November 21, 2018
Novel monoamine oxidase inhibitors based on the privileged 2-imidazoline molecular frameworkAnton Shetnev, Angelina Osipyan, Sergey Baykov, et al.
European Journal of Medicinal Chemistry|October 14, 2025
Extending the chemical space of glutarimide-based cereblon ligands through an efficient Rh(II)-catalyzed X-H insertion reactionEkaterina Levashova, Luca Bischof, Alexander Bunev, et al.
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