380415-68-9Relevant academic research and scientific papers
Tandem cyclization of o-alkynylanilines with isocyanides triggered by intramolecular nucleopalladation: Access to heterocyclic fused 2-aminoquinolines
Wu, Wanqing,Li, Meng,Zheng, Jia,Hu, Weigao,Li, Chunsheng,Jiang, Huanfeng
supporting information, p. 6855 - 6858 (2018/06/26)
Herein, a novel strategy for the synthesis of various heterocyclic fused 2-aminoquinolines via palladium-catalyzed tandem cyclization of o-alkynylanilines with isocyanides has been developed. This process includes trans-oxy/aminopalladation, isocyanide in
Sc(OTf)3-catalyzed bicyclization of o-alkynylanilines with aldehydes: Ring-fused 1, 2-dihydroquinolines
Zhu, Can,Ma, Shengming
supporting information, p. 13532 - 13535 (2015/02/19)
A Sc(OTf)3-catalyzed cascade Prins-type cyclization reaction of o-alkynylanilines, bearing a hydroxy or amine functionality, with aldehydes affords 1, 2-dihydroquinoline derivatives having an extra fused ring efficiently under mild reaction con
Discovery, synthetic methodology, and biological evaluation for antiphotoaging activity of bicyclic[1,2,3]triazoles: In vitro and in vivo studies
Hsieh, Hsin-Yu,Lee, Wen-Chun,Senadi, Gopal Chandru,Hu, Wan-Ping,Liang, Jium-Jia,Tsai, Tong-Rong,Chou, Yu-Wei,Kuo, Kung-Kai,Chen, Chung-Yu,Wang, Jeh-Jeng
supporting information, p. 5422 - 5435 (2013/07/26)
Novel bicyclic[1,2,3]triazoles (4, 7, 11, 15) have been synthesized using a one-pot metal free strategy with high structural diversity as photoprotective agents, and their effect on UVA-induced senescence in human dermal fibroblast cells (FB) and the asso
Novel peptidomimetics of the antifungal cyclic peptide rhodopeptin: Synthesis of mimetics and their antifungal activity
Nakayama, Kiyoshi,Kawato, Haruko C.,Inagaki, Hiroaki,Ohta, Toshiharu
, p. 3451 - 3454 (2007/10/03)
(matrix presented) Novel peptidomimetics of the antifungal cyclic peptide Rhodopeptin were synthesized. As with the cyclic peptides, the presence of all three Rhodopeptin side chains was found to be indispensable for peptidomimetic activity. We discovered
