Daniel L Priebbenow
Affiliations: | Deakin University, Burwood, Victoria, Australia |
Area:
Synthetic Organic ChemistryGoogle:
"Daniel Priebbenow"Mean distance: (not calculated yet)
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Barbaro L, Nagalingam G, Triccas JA, et al. (2022) Discovery of Anti-tubercular Analogues of Bedaquiline with Modified A-, B- and C-Ring Subunits. Chemmedchem. e202200533 |
Priebbenow DL, Hua C. (2021) Acyl silane directed Cp*Rh(III)-catalysed alkylation/annulation reactions. Chemical Communications (Cambridge, England) |
Barbaro L, Nagalingam G, Triccas JA, et al. (2021) Synthesis and evaluation of pyridine-derived bedaquiline analogues containing modifications at the A-ring subunit. Rsc Medicinal Chemistry. 12: 943-959 |
Priebbenow DL, Mathiew M, Shi DH, et al. (2021) Discovery of Potent and Fast-Acting Antimalarial Bis-1,2,4-triazines. Journal of Medicinal Chemistry |
Priebbenow DL, Leaver D, Nguyen N, et al. (2020) Discovery of Acylsulfonohydrazide-Derived Lysine Acetyltransferase (KAT6A) Inhibitors as Potent Senescence-Inducing Anti-Cancer Agents. Journal of Medicinal Chemistry |
Priebbenow DL. (2020) Silicon‐Derived Singlet Nucleophilic Carbene Reagents in Organic Synthesis Advanced Synthesis & Catalysis. 362: 1927-1946 |
Leaver D, Cleary B, Nguyen NT, et al. (2019) Discovery of benzoylsulfonohydrazides as potent inhibitors of the histone acetyltransferase KAT6A. Journal of Medicinal Chemistry |
Deora GS, Qin C, Vecchio E, et al. (2019) Substituted Pyridazin-3(2H)-ones as Highly Potent and Biased Formyl Peptide Receptors Agonists. Journal of Medicinal Chemistry |
Priebbenow DL, Barbaro L, Baell JB. (2016) New synthetic approaches towards analogues of bedaquiline. Organic & Biomolecular Chemistry. 14: 9622-9628 |
Lamers P, Priebbenow DL, Bolm C. (2016) ChemInform Abstract: Iron-Catalyzed Acylative Dealkylation of N-Alkylsulfoximines. Cheminform. 47 |