Search results for "Benzyl"
showing 10 items of 878 documents
CCDC 1427937: Experimental Crystal Structure Determination
2017
Related Article: Luca Leoni, Rakesh Puttreddy, Ondřej Jurček, Andrea Mele, Ilaria Giannicchi, Francesco Yafteh Mihan, Kari Rissanen, Antonella Dalla Cort|2016|Chem.-Eur.J.|22|18714|doi:10.1002/chem.201604313
CCDC 1033416: Experimental Crystal Structure Determination
2015
Related Article: Ayan Patra, Shobhraj Haldar, Gonela Vijay Kumar, Luca Carrella, Aloke Kumar Ghosh, Manindranath Bera|2015|Inorg.Chim.Acta|436|195|doi:10.1016/j.ica.2015.07.039
CCDC 115540: Experimental Crystal Structure Determination
2000
Related Article: M.Schurmann, A.Silvestri, G.Ruisi, M.A.Girasolo, A.B.Paulsen, F.Huber, R.Barbieri|1999|J.Organomet.Chem.|584|293|doi:10.1016/S0022-328X(99)00166-7
CCDC 840684: Experimental Crystal Structure Determination
2013
Related Article: E.Laurila,L.Oresmaa,E.Kalenius,P.Hirva,M.Haukka|2013|Polyhedron|52|1231|doi:10.1016/j.poly.2012.06.036
CCDC 2066260: Experimental Crystal Structure Determination
2021
Related Article: Tushar S. Basu Baul, Anurag Chaurasiya, Banteilang Lyngdoh Nonglait, Antonin Lyčka, Dieter Schollmeyer, Klaus Jurkschat|2021|J.Organomet.Chem.|946-947|121898|doi:10.1016/j.jorganchem.2021.121898
CCDC 1590298: Experimental Crystal Structure Determination
2018
Related Article: Petr Švec, Hélène Cattey, Zdeňka Růžičková, Josef Holub, Aleš Růžička, Laurent Plasseraud|2018|New J.Chem.|42|8253|doi:10.1039/C7NJ05058E
CCDC 831306: Experimental Crystal Structure Determination
2012
Related Article: M.Giese, M.Albrecht, G.Ivanova, A.Valkonen, K.Rissanen|2012|Supramol.Chem.|24|48|doi:10.1080/10610278.2011.622384
The introduction of fluorine atoms or trifluoromethyl groups in short cationic peptides enhances their antimicrobial activity
2006
The effect of introducing fluorine atoms or trifluoromethyl groups in either the peptidic chain or the C-terminal end of cationic pentapeptides is reported. Three series of amide and ester peptides were synthesised and their antimicrobial properties evaluated. An enhanced activity was found in those derivatives whose structure contained fluorine, suggesting an increase in their hydrophobicity.
Synthesis and Reactivity toward Isonitriles of (2-Aminoaryl)palladium(II) Complexes
2001
Mixtures of “Pd(dba)2” (dba = dibenzylideneacetone) and 2,2‘-bipyridine (bpy; 1:2) or N,N,N‘,N‘-tetramethylethylenediamine (tmeda; 1:1) react with 2-bromo-4-nitroaniline to give [Pd{C6H3NH2-2-NO2-5}Br(N−N)] (N−N = bpy (1b), tmeda (1b‘)). Reactions of 2-iodoaniline with mixtures of “Pd(dba)2” and isonitriles RNC (R = C6H3Me2-2,6 (Xy), 2:1:2 molar ratios; R = tBu, 2.9:1:2 molar ratios) result in the formation of the complexes [Pd{κ2C,N-C(NXy)C6H4NH2-2}I(CNXy)] (2a) and trans-[Pd{C(NtBu)C6H4NH2-2}I(CNtBu)2] (3a*). The reactions of [Pd{C6H4NH2-2}I(bpy)] and 1b‘ with RNC give the complexes trans-[Pd{C(NR)C6H3NH2-2-Y-5}}X(CNR)2] (Y = H, X = I, R = Xy (3a), tBu (3a*); Y = NO2, X = Br, R = Xy (3b),…
Gold(I) Biscarbene Complexes Derived from Vascular-Disrupting Combretastatin A-4 Address Different Targets and Show Antimetastatic Potential
2014
Gold N-heterocyclic carbene (NHC) complexes are an emerging class of anticancer drugs. We present a series of gold(I) biscarbene complexes with NHC ligands derived from the plant metabolite combretastatin A-4 (CA-4) that retain its vascular-disrupting effect, yet address different cellular and protein targets. Unlike CA-4, these complexes did not interfere with tubulin, but with the actin cytoskeleton of endothelial and cancer cells. For the highly metastatic 518A2 melanoma cell line this effect was accompanied by a marked accumulation of cells in the G1 phase of the cell cycle and a suppression of active prometastatic matrix metalloproteinase-2. Despite these mechanistic differences the co…