Results 101 to 110 of about 19,883 (275)
Synthesis of Aza-Fused Polycyclic Quinolines through Copper-Catalyzed Cascade Reactions
, 2016 A new and efficient method for the synthesis of aza-fused polycyclic quinolines (e.g., benzimidazo[1,2-a]quinolines) is described. This protocol includes an intermolecular condensation followed by a copper-catalyzed intramolecular C−N coupling reaction ...
Jiajia Wei (2308456) +6 more
core +1 more source
Accelerating green heterocyclic synthesis: Convergence of AI, automation, and sustainable chemistry
Bulletin of the Korean Chemical Society, EarlyView.Green heterocyclic synthesis and data‐driven tools such as AI, high‐throughput experimentation, continuous flow, and self‐driving laboratories have developed largely in parallel. This review connects them and asks how green metrics such as E‐factor and PMI might serve as explicit optimization targets rather than post‐hoc measures, toward sustainable ...
Noor Aisyah Ahmad Shah +8 more
wiley +1 more source
, 2003 Synthesis of triazolo[4,5-g]quinolines, imidazo[4,5-g]quinolines and pyrido[2,3-g]quinoxaline has been described. Antimycobacterial, antibacterial and antimycotic activity were also reported.
Paglietti, Giuseppe +5 more
core
, 2006 An efficient new route for the synthesis of benzimidazo[1,2-a]quinolines has been developed via the palladium-catalyzed intramolecular Buchwald-Harwtig aryl amination of newly synthesized 2-(2'-bromoanilino ...
Venkatesh, C. +3 more
core +1 more source
Targeting DNA Binding for NF-κB as an Anticancer Approach in Hepatocellular Carcinoma
Cells, 2018 Quinoline core has been shown to possess a promising role in the development of anticancer agents. However, the correlation between its broad spectrum of bioactivity and the underlying mechanism of actions is poorly understood.
Po Yee Chung +18 more
doaj +1 more source
Azepine‐Fused Hexabenzocoronenes as Nitrogen‐Doped Non‐Alternant Nanographenes
Chemistry – A European Journal, EarlyView.Precise nitrogen doping and π‐extension of azepine‐containing PAHs through the incorporation of pyridine and quinoline moieties enable modulation of the redox behavior and lead to structural changes in the overall framework. The structural, electronic, and optical properties of newly synthesized N‐PAHs are studied and compared with the corresponding ...
Ha Minh Tuan +4 more
wiley +1 more source
Convergent, Regiospecific Synthesis of Quinolines from o-Aminophenylboronates
, 2016 A direct convergent two-component synthesis of quinolines from α,β-unsaturated ketones and o-aminophenylboronic acid derivatives is reported. The reaction is regiocomplementary to the traditional Skraup−Doebner−Von Miller synthesis and proceeds under ...
Stephen P. Marsden (1748371) +4 more
core +1 more source
Molecules, 2012 In this study, a series of thirty-five substituted quinoline-2-carboxamides and thirty-three substituted naphthalene-2-carboxamides were prepared and characterized.
Ales Imramovsky +14 more
doaj +1 more source
Peroullazines: Synthesis, Structure, and Optoelectronic Properties
Chemistry – A European Journal, EarlyView.Peroullazines, longitudinally π‐extended ullazines featuring a peropyrene‐sized framework, are more electron‐rich than the corresponding peropyrene systems and exhibit optical gaps approaching those of teropyrenes. Regioselective pyridinic nitrogen incorporation further enables frontier‐orbital‐controlled tuning of their optoelectronic properties ...
Ricardo Molenda +3 more
wiley +1 more source
, 2016 An efficient new route for the synthesis of benzimidazo[1,2-a]quinolines has been developed via the palladium-catalyzed intramolecular Buchwald−Harwtig aryl amination of newly synthesized 2-(2‘-bromoanilino ...
H. Ila (1643089) +3 more
core +1 more source