Results
1 -
10 of
4762
(Click
here to explore results)
- Isoquinoline gas-phase absorption spectrum in the vacuum ultraviolet between 3.7 and 10.7 eV. New valence and Rydberg electronic states. Sydney Leach, Nykola C. Jones, Søren V. Hoffmann, Sun Un
, RSC Adv.
, 2019
, 9
, 5121
- Palladium-catalyzed enolate arylation as a key C–C bond-forming reaction for the synthesis of isoquinolines. Ben S. Pilgrim, Alice E. Gatland, Carlos H. A. Esteves, Charlie T. McTernan, Geraint R. Jones, Matthew R. Tatton, Panayiotis A. Procopiou, Timothy J. Donohoe
, Org. Biomol. Chem.
, 2016
, 14
, 1065
- Selective removal of isoquinoline and quinoline from simulated fuel using 1,1′-binaphthyl-2,2′-diol (BINOL): crystal structure and evaluation of the adduct electronic properties. Adeniyi S. Ogunlaja, Eric Hosten, Richard Betz, Zenixole R. Tshentu
, RSC Adv.
, 2016
, 6
, 39024
- Rhodium-catalyzed oxidative annulation of 1H-indazoles with alkynes for the synthesis of indazolo[3,2-a]isoquinolines via C–H bond functionalization. Jian Huang, Yang Fu, Zhihong Deng, Wei Chen, Zhibin Song, Yiyuan Peng
, Org. Biomol. Chem.
, 2020
, 18
, 9863
- In situ air oxidation and photophysical studies of isoquinoline-fused N-heteroacenes. Amol D. Sonawane, Rohini A. Sonawane, Khin Myat Noe Win, Masayuki Ninomiya, Mamoru Koketsu
, Org. Biomol. Chem.
, 2020
, 18
, 2129
- Lauraceae alkaloids. Dayana Lacerda Custódio, Valdir Florêncio da Veiga Junior
, RSC Adv.
, 2014
, 4
, 21864
- Synthesis and antitubercular activity of 1- and 3-substituted benzo[g]isoquinoline-5,10-diones. Robert J. Smets, Eveline Torfs, Filip Lemière, Paul Cos, Davie Cappoen, Kourosch Abbaspour Tehrani
, Org. Biomol. Chem.
, 2019
, 17
, 2923
- Recent progress in the synthesis of pyrrolo[2,1-a]isoquinolines. Hai-Lei Cui
, Org. Biomol. Chem.
, 2022
, 20
, 2779
- Fluorescence enhancement of quinolines by protonation. Essi Tervola, Khai-Nghi Truong, Jas S. Ward, Arri Priimagi, Kari Rissanen
, RSC Adv.
, 2020
, 10
, 29385
- Exploring radiative and nonradiative decay paths in indole, isoindole, quinoline, and isoquinoline. Yu Harabuchi, Kenichiro Saita, Satoshi Maeda
, Photochem. Photobiol. Sci.
, 2018
, 17
, 315