Results 181 to 190 of about 19,883 (275)

Chlorination of Quinoline Derivatives

YAKUGAKU ZASSHI, 1973
T, Kato, H, Yamanaka, T, Shimizu
openaire   +3 more sources

Regiodivergent C3 and C4 Amination of Quinolines via Radical and Ionic Pathways. [PDF]

Angew Chem Int Ed Engl
Kim YE, Kim J, Lee J, Hong S.
europepmc   +1 more source

Recent Advances in Microwave and Ultrasound Assisted Synthesis of Quinoline Derivatives as Anticancer Agents. [PDF]

Chem Biodivers
Pal R, Matada GSP, Teli G, B V M, Pandey VK, Pratap S.   +5 more
europepmc   +1 more source

Occurrence and Washout of Health-Hazardous Chemicals in Children's Clothing. [PDF]

Contact Dermatitis
Dostberg A, Åström T, Sadiktsis I, Östman C, Nilsson U.   +4 more
europepmc   +1 more source

Quinoline Derivatives. (6)

YAKUGAKU ZASSHI, 1962
Y, HAMADA, H, SUGIHARA, T, ISOBE
openaire   +3 more sources

Theranostic Potential of an NAD(P)H‐Activatable Fluorophore: Assessing Cancer Aggressiveness and Triggering Apoptosis

Angewandte Chemie, Volume 138, Issue 42, 12 October 2026.
DE‐CQ, an NAD(P)H‐activatable theranostic probe, enables the quantification of cancer aggressiveness via glucose‐stimulated fluorescence imaging and selectively induces apoptosis. Its multifaceted efficacy is demonstrated across 2D cells, 3D spheroids, and in vivo models.
Yujin Cha, Taehoon Oh, Hui Joo Kim, Minju Kang, Shin A Yoon, Yul Lee, Yeon‐Ju Lee, Sun Young Park, Dong‐Sik Shin, Sung‐Kyun Ko, Jiyou Han, Min Hee Lee   +11 more
wiley   +2 more sources

A Rh(II) Catalyzed Atropisomer Selective Ring Expansion of 3-Aryl Indoles to 4-Aryl Quinolines. [PDF]

ACS Catal
Basilaia M, Zanolini R, Dogan NK, Rustin G, Regganie T, Susskind NJ, Gustafson J, Mao Y.   +7 more
europepmc   +1 more source

Discrepancy in Reported and Observed Monoacylglycerol Lipase Inhibition of Aryl Formyl Piperidine Containing Potent and Highly Selective Monoacylglycerol Lipase Inhibitor

ChemMedChem, Volume 21, Issue 19, 14 October 2026.
A reported potent and selective reversible MAGL inhibitor fails to reproduce its claimed potency in two established in vitro assays, even when the previously reported substrate is used, while eight related analogs are likewise inactive. The findings highlight substantial assay‐dependent behavior and the need for careful validation before such compounds
Juha R. Savinainen, Praveen Kumar Singh, Jari Yli‐Kauhaluoma, Jayendra Z. Patel   +3 more
wiley   +1 more source

Photochemical C4-Selective C-H Amination of Quinolines via <i>N</i>-Shift of Heteroaryl Azides. [PDF]

Org Lett
Dimasi A, Montoli A, Macetti G, Lo Presti L, Passarella D, Fasano V.   +5 more
europepmc   +1 more source

The Expanding Role of Diazirines in Synthetic Methodology

European Journal of Organic Chemistry, Volume 29, Issue 38, 13 October 2026.
Beyond their established role in photoaffinity labeling, diazirines have emerged as versatile reagents in synthetic chemistry. This review highlights their dual reactivity as carbene and nitrogen‐transfer precursors, showcasing mechanistic insights and diverse applications in cyclopropanations, cycloadditions, skeletal editing, amination, heterocycle ...
Viktor Savic, Dominik Schnalzer, Marko D. Mihovilovic, Michael Schnürch   +3 more
wiley   +1 more source