112500-20-6Relevant articles and documents
Synthesis and Photocleavage of Quinoline Methyl Ethers: A Mild and Efficient Method for the Selective Protection and Deprotection of the Alcohol Functionality
Provatas, Anthony A.,Epling, Gary A.,Stuart, James D.
, p. 763 - 769 (2016/08/09)
The synthesis and photocleavage of quinolinyl methyl ether-protected alcohols is reported in this study. A variety of quinoline methyl chlorides were synthesized, and protection of the various alcohols was performed via a substitution reaction in the presence of a strong base. Photocleavage of the quinolinyl methyl ether moiety proceeded under visible light with the formation of the charged quinolinyl radical intermediate through a single-electron transfer in the presence of a photosensitizer dye leading to the deprotected alcohol in excellent yields. The utility of triethylamine as a sacrificial reductant and d-sorbitol as a radical scavenger were also investigated in this study.
Sulfur-Containing 2-Arylquinolinemethanols as Potential Antimalarials
Epling, Gary A.,Lin, Kuei-Ying
, p. 853 - 857 (2007/10/02)
The synthesis and antimalarial activity of six new 2-arylquinoline-4-methanols is described.The compounds bearing a sulfur were prepared to determine if antimalarial activity can be retained while photoreactivity and phototoxicity is diminished by such su
