Atroposelective Synthesis of Biaryl N‐Oxides via Cu‐Catalyzed De Novo Heteroaromatic N‐Oxide Ring Formation.

Autor: Ma, Ke¹ (AUTHOR), Qi, Ting² (AUTHOR), Hu, Lei^1,3 (AUTHOR), Chen, Chen¹ (AUTHOR), Wang, Wan¹ (AUTHOR), Li, Jun‐Long² (AUTHOR), Peng, Cheng¹ (AUTHOR), Zhan, Gu¹ (AUTHOR) zhangu@cdutcm.edu.cn, Han, Bo¹ (AUTHOR) hanbo@cdutcm.edu.cn

Publikováno v: Advanced Science. 10/28/2024, Vol. 11 Issue 40, p1-12. 12p.

[1,2,4]Triazolo[1,5-c]pyrimidines as Tools to Investigate A 3 Adenosine Receptors in Cancer Cell Lines.

Autor: Federico S; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Persico M; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Trevisan L; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Biasinutto C; Department of Life Sciences, University of Trieste, Via Licio Giorgieri 5, 34127, Trieste, Italy., Bolcato G; Molecular Modeling Section (MMS), Department of Pharmaceutical and Pharmacological Sciences, University of Padova, via Marzolo 5, 35131, Padova, Italy., Salmaso V; Molecular Modeling Section (MMS), Department of Pharmaceutical and Pharmacological Sciences, University of Padova, via Marzolo 5, 35131, Padova, Italy., Da Ros T; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Gianferrara T; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Prencipe F; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy., Kachler S; Rudolf-Virchow-Zentrum -, Center for Integrative and Translational Bioimaging, University of Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Germany., Klotz KN; Institut für Pharmakologie und Toxikologie, University of Würzburg, Versbacher Str. 9, 97078, Würzburg, Germany., Pacor S; Department of Life Sciences, University of Trieste, Via Licio Giorgieri 5, 34127, Trieste, Italy., Moro S; Molecular Modeling Section (MMS), Department of Pharmaceutical and Pharmacological Sciences, University of Padova, via Marzolo 5, 35131, Padova, Italy., Spalluto G; Department of Chemical and Pharmaceutical Sciences, University of Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy.

Publikováno v: ChemMedChem [ChemMedChem] 2023 Nov 02; Vol. 18 (21), pp. e202300299. Date of Electronic Publication: 2023 Sep 22.

ChemInform Abstract: APORPHINES PART 8, TOTAL SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF (+-)-APOMORPHINE, (+-)-APOCODEINE, (+-)-N-N-PROPYLNORAPOMORPHINE, AND (+-)-N-N-PROPYLNORAPOCODEINE

Autor: J. L. NEUMEYER, B. R. NEUSTADT, H. OH. KYUNG, K. K. WEINHARDT, C. B. BOYCE, F. J. ROSENBERG, D. G. TEIGER

Publikováno v: Chemischer Informationsdienst. 5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1b3042bab356bc3f8e11826660e59dbb
https://doi.org/10.1002/chin.197409485

Aporphines. V. Total synthesis of (plus or minus)-apomorphine

Autor: J L, Neumeyer, B R, Neustadt, K K, Weinhardt

Publikováno v: Journal of pharmaceutical sciences. 59(12)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::50278a600aa65d6e07f15421dca8e260
https://pubmed.ncbi.nlm.nih.gov/5509871

Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope.

Autor: Kischkewitz, Marvin¹ (AUTHOR), Marinic, Bruno¹ (AUTHOR), Kratena, Nicolas¹ (AUTHOR), Lai, Yonglin¹ (AUTHOR), Hepburn, Hamish B.¹ (AUTHOR), Dow, Mark² (AUTHOR), Christensen, Kirsten E.¹ (AUTHOR), Donohoe, Timothy J.¹ (AUTHOR) timothy.donohoe@chem.ox.ac.uk

Publikováno v: Angewandte Chemie. 7/4/2022, Vol. 134 Issue 27, p1-10. 10p.