Results 61 to 70 of about 3,985 (232)

Rapid Access to Emission‐Tunable Organelle‐Targeted Aggregation‐Induced Emission Luminogens Through One‐Pot Skeletal Editing

Transformative Chemistry, Volume 1, Issue 1, December 2025.
Herein we report a skeletal editing strategy for rapidly transforming readily available isoquinolines into synthetically challenging (dihydrodibenzo[c,i]phenanthridin‐6‐yl)diphenylphosphine oxides (DHBPPO) derivatives. These DHBPPO derivatives exhibit tunable emission, aggregation‐induced emission (AIE) properties, organelle‐targeted specificity, and ...
Yanling Liu, Chaoyang Li, Yunlong Qin, Yifan Cheng, Jianing Zhang, Yang Zhao, Tianhao Wu, Chenghan He, Cheng Xu, Qilin Wang, Zheng Zhao, Ben Zhong Tang   +11 more
wiley   +1 more source

Mise en évidence d'une résistance aux trypanocides parmi des souches de Trypanosoma congolense récemment isolées au Burkina [PDF]

, 1984
Dix-huit souches de T. congolense ont fait l'objet d'une épreuve de sensibilité à l'acétate de diminazène et à l'isométamidium chez la souris. L'intérêt et les limites de cette épreuve sont discutés. Les 13 souches de T.
Authié, Edith
core  

In Pursuit of Low Energy Phosphorescence: Late Metal Coordination Complexes of the Planar, π‐extended Bipyridyl Ligand 6,6′,7,7′‐Biphenanthridine

Chemistry – A European Journal, Volume 31, Issue 63, November 12, 2025.
Abstract The coordination chemistry of the planar, doubly π‐extended bipyridine analog, 6,6′,7,7′‐biphenanthridine (p‐biphe), is presented. The phenanthridine units in p‐biphe are fused together at the 6‐ and 7‐ positions, and the resulting rigid ligand is compared with the more flexible parent “biphe” fused only at the 6‐positions.
Dion B. Nemez, Robert J. Ortiz, Keighlynn A. Veilleux, J. A. Gareth Williams, David E. Herbert   +4 more
wiley   +1 more source

A terc-amino effektus vizsgálata és kiterjesztése: új típusú, biológiailag aktív policiklusos vegyületek előállítása = The study and the extension of the tert-amino effect: Synthesis of new types of polycyclic compounds with biological activities [PDF]

, 2013
1. Vizsgáltuk a terc-amino effektus 2. típusának kiterjesztését a reakcióban résztvevő vinil és terc-amino csoportot két külön gyűrűn tartalmazó (kondenzált) bi- és triaril - bifenil/fenilpiridazin, trifenil/difenilpiridazin, naftalin illetve ...
Balogh, Balázs, Czompa, Andrea, Dunkel, Petra, Halászné Dajka, Beáta, Krajsovszky, Gábor, Mátyus, Péter, Tapolcsányi, Pál, Túrós, György István, Éliás, Olivér   +8 more
core  

Palladium–mediated organofluorine chemistry [PDF]

, 2014
Producción CientíficaThe substitution of fluorine for hydrogen in a molecule may result in profound changes in its properties and behaviour. Fluorine does not introduce special steric constraints since the F atom has a small size. However, the changes in
Adonis, Akkerman, Albeniz, Albeniz, Albeniz, Albeniz, Albe´niz, Albe´niz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Albéniz, Algarra, Alonso, Amii, Anstaett, Ara, Aspin, Babudri, Bahmanyar, Bakhmutov, Ball, Ball, Ball, Bandini, Barluenga, Beweries, Birkholz, Bonaterra, Bosque, Braun, Braun, Braun, Braun, Breyer, Breyer, Brisdon, Brothers, Bélanger, Cardone, Cargill, Carrera, Carrio´n, Carsten, Casado, Casado, Casado, Casado, Casado, Casado, Casado, Casado, Casares, Casares, Casares, Casares, Casares, Casares, Chan, Chaouche, Chen, Chen, Chen, Chen, Chen, Chen, Cho, Cho, Clot, Clot, Collings, Cronin, Csapó, Culkin, Dankwardt, Darses, Davis, Deeg, delPozo, delPozo, Dilman, Doyle, Du, Dutheuil, Eddarir, Eisenberger, Engle, Erb, Espinet, Espinet, Fan, Fan, Fan, Fang, Feng, Feng, Feng, Feng, Filippini, Filippini, Flemming, Fraser, Frohn, Frohn, Fuentes, Fujikawa, Fukuzumi, Furuya, Furuya, Furuya, Garcia-Melchor, García-Cuadrado, García-Monforte, García-Monforte, Gerfaud, Gorelski, Granberg, Grushin, Grushin, Grushin, Grushin, Grushin, Grushin, Grushin, Grushin, Guihaumé, Guo, Gurung, Gurung, Hajipour, Hamashima, Hamashima, Hamashima, Hartwig, Hazari, He, He, He, Heinze, Heitz, Hollingworth, Huang, Huang, Hudlicky, Hughes, Hughes, Hughes, Hull, Högermeier, Ichikawa, Ichikawa, Ishihara, Ishikawa, Jakt, Jasim, Jiang, Jiao, Jin, Johnson, Kakino, Kamer, Kashiwabara, Kaspi, Katcher, Katcher, Kawatsura, Kieltsch, Kim, Kim, Kim, Kiplinger, Kirsch, Kitazume, Kitazume, Kitazume, Komatsu, Korenaga, Koroniak, Kuehnel, Kurosawa, Lafrance, Lafrance, Lanteri, Larini, Lechel, Lee, Lee, Lee, Leng, Li, Li, Li, Li, Liang, Liang, Lim, Liu, Liu, Liu, Liu, Liu, Liu, Liu, Loo, Loy, Lundgren, Luo, Ma, Ma, Macgregor, Maimone, Manabe, Marshall, Marshall, Martínez-Arranz, Martínez-Prieto, Matoušek, Matsubara, Mazzotti, McClinton, Mikami, Min, Molina de la Torre, Motoda, Mu, Mu, Murphy, Narumi, Nguyen, Ni, Nie, Niedermann, Nova, Nova, Noël, Ohashi, Ohashi, Ohashi, Ojima, Orbach, Orbach, Pan, Paquin, Paull, Peng, Pigeon, Pilon, Powers, Powers, Prakash, Prakash, Purser, Pérez-Rodríguez, Pérez-Temprano, Pérez-Temprano, Pérez-Temprano, Pérez-Temprano, Qing, Qiu, Qiu, Qiu, Qui, Racowski, Racowski, Robbins, Roche, Roche, Roe, Roemer, Roy, Ruppert, Sabater, Saeki, Sakakura, Sakoda, Sato, Sato, Scharf, Schaub, Sharif, Shen, Sheppard, Shigeoka, Shimizu, Stuart, Sun, Sun, Surapanich, Taguchi, Tannaci, Tellier, Tomashenko, Torrens, Uberman, Uberman, Ukisu, Umemoto, Usón, Usón, Usón, Usón, Usón, Usón, Usón, van Asselt, Vigalok, Von Werner, Wang, Wang, Wang, Wang, Watson, Wei, Widdovson, Widdovson, Wilhelm, Wilson, Wu, Wójtowicz-Rajchel, Xu, Xu, Yahav, Yamada, Yandulov, Yang, Yang, Yang, Yang, Yang, Yang, Yang, Ye, Ye, Yokomatsu, Yokota, Yu, Yu, Yu, Yuan, Zatolochnaya, Zemmouri, Zhang, Zhang, Zhang, Zhao, Zhao, Zhao, Zhu   +360 more
core   +2 more sources

Multistep Reactions Initiated by Amine‐Based Organometallic Methods

European Journal of Organic Chemistry, Volume 28, Issue 40, October 29, 2025.
The advent of C–H activation and other organometallic methodologies making use of transient directing groups or free amines themselves for the elaboration of amine substrates provides unique access to cascade‐type reactions that can generate significant molecular complexity in one pot. The pursuit of atom‐ and step‐economical pathways to access complex
Victoria D. Ho, Olutayo N. Farinde, Kendra K. Shrestha, Michael C. Young   +3 more
wiley   +1 more source

Studies in the phenanthridine series. Part IV. 1:10-dimethyl phenanthridines

Journal and proceedings of the Royal Society of New South Wales, 1945
(Uploaded by Plazi from the Biodiversity Heritage Library) No abstract provided.
openaire   +1 more source

Trypanosoma brucei aquaglyceroporin 2 is a high-affinity transporter for pentamidine and melaminophenyl arsenic drugs and the main genetic determinant of resistance to these drugs [PDF]

, 2017
Objectives Trypanosoma brucei drug transporters include the TbAT1/P2 aminopurine transporter and the high-affinity pentamidine transporter (HAPT1), but the genetic identity of HAPT1 is unknown. We recently reported that loss of T. brucei aquaglyceroporin
Aguinaga Andrés, David, Baker, Nicola, Barrett, Michael P., Burchmore, Richard J. S., Clucas, Caroline, De Koning, Harry P., Eze, Anthonius A., Glover, Lucy, Graf, Fabrice E., Horn, David, Lee, Rebecca S., Ludin, Philipp, MacLeod, Annette, McDonald, Jennifer, Munday, Jane C., Mäser, Pascal, Natto, Manal J., Tait, Andy, Teka, Ibrahim A., Turner, C. Michael R.   +19 more
core  

Visible Light-assisted Deconstruction/Refunctionalization of Strained and Unstrained N-Cycloalkylanilines [PDF]

, 2022
The exploitation of ring strain as a driving force to facilitate chemical reactions is a well-appreciated principle in organic chemistry. Of the strained carbocycles frequently explored in this respect, cyclopropane ring systems have drawn considerably ...
Boateng, Elvis Duah
core   +1 more source

Synthesis of Quinolino[4,3‐ j]phenanthridines and their Photophysical Characterization [PDF]

Quinolino[4,3-j]phenanthridines were synthesized from para-terphenyl-2,2′′-diamines, which were obtained by cross-coupling reactions. The diamines were converted into amides and ortho-cyclized to quinolino[4,3-j]phenanthridines using Morgan-Walls ...
Podlech, Joachim, Schumann, Felix R.
core   +2 more sources