Results 161 to 170 of about 18,253 (267)
Regiodivergent C3 and C4 Amination of Quinolines via Radical and Ionic Pathways. [PDF]
Kim YE, Kim J, Lee J, Hong S.
europepmc +1 more source
Quinoline and Acridine Synthesis [PDF]
openaire +1 more source
Sterisch überfrachtete Alken‐Photo‐Redox‐Schalter auf Basis von Chinolinium/Carben Bausteinen
Eine modulare Synthese einer neuen Klasse von Photo‐ und Redox‐Schaltern wird beschrieben, die auf der Kombination von Chinoliniumsalzen und Carbenen basiert. Das photochemische Schalten ermöglicht einen selektiven Wechsel zwischen gefalteten E/Z‐Isomeren, während das elektrochemische Schalten den Wechsel zwischen neutralen, radikalkationischen und ...
Chris Burdenski +10 more
wiley +1 more source
A Rh(II) Catalyzed Atropisomer Selective Ring Expansion of 3-Aryl Indoles to 4-Aryl Quinolines. [PDF]
Basilaia M +7 more
europepmc +1 more source
Photochemical C4-Selective C-H Amination of Quinolines via <i>N</i>-Shift of Heteroaryl Azides. [PDF]
Dimasi A +5 more
europepmc +1 more source
Overcrowded Alkene Photo‐Redox‐Switches Based on Quinolinium/Carbene Building Blocks
A modular synthesis of a new class of photo‐ and redox‐switches is described based on the combination of quinolinium salts and carbenes. Photochemical switching allows to selectively switch between folded E/Z isomers, while electrochemical switching allows to change between neutral, radical cation and dicationic oxidation states, which are all isolable
Chris Burdenski +10 more
wiley +1 more source
An approach to prepare pyrido[2,1‐a]isoindoles via the cycloaddition of pyridine‐based 1,3‐dipoles and benzyne is described, offering modular access to a range of substituted products by systematic tuning of the dipole. A modular strategy for the synthesis of fused indolizine/isoindole hybrids, pyrido[2,1‐α]isoindoles, via cycloaddition of pyridine ...
Samira Taghizadeh Nodehi +2 more
wiley +1 more source
Regioselective Iridium-Catalyzed C(7)-H Borylation of Free <i>N</i>-H 6‑Fluoroquinolones. [PDF]
Courtney E +6 more
europepmc +1 more source
Conformational restriction strategies to increase the activity and selectivity of the STAT5b inhibitor Stafib‐2 are presented. The best conformationally restricted inhibitor Stafib‐2‐CR has threefold higher activity against STAT5b than Stafib‐2. A cell‐permeable prodrug of Stafib‐2‐CR inhibits phosphorylation of STAT5b in cultured human leukemia cells ...
Theresa Münzel +5 more
wiley +1 more source

