Search results for "ferrocenyl"

showing 10 items of 89 documents

CCDC 1417556: Experimental Crystal Structure Determination

2015

Related Article: Tania Romero-Morcillo, Francisco Javier Valverde-Muñoz, Lucía Piñeiro-López, M. Carmen Muñoz, Tomás Romero, Pedro Molina, José A. Real|2015|Dalton Trans.|44|18911|doi:10.1039/C5DT03084F

Space GroupCrystallographybis(2-(1-Ferrocenyl-1H-123-triazol-4-yl)pyridine)-bis(isoselenocyanato)-iron(ii) chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1417555: Experimental Crystal Structure Determination

2015

Related Article: Tania Romero-Morcillo, Francisco Javier Valverde-Muñoz, Lucía Piñeiro-López, M. Carmen Muñoz, Tomás Romero, Pedro Molina, José A. Real|2015|Dalton Trans.|44|18911|doi:10.1039/C5DT03084F

Space GroupCrystallographybis(2-(1-Ferrocenyl-1H-123-triazol-4-yl)pyridine)-bis(isoselenocyanato)-iron(ii) chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 956710: Experimental Crystal Structure Determination

2014

Related Article: Kristina Hüttinger, Christoph Förster, Katja Heinze|2014|Chem.Commun.|50|4285|doi:10.1039/C3CC46919K

Space GroupCrystallographybis(2-(Ferrocenyliminomethyl)pyrrolyl)-dioxo-molybdenum toluene solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1843133: Experimental Crystal Structure Determination

2018

Related Article: Christoph Förster, Patrick M. Becker, Katja Heinze|2018|Z.Anorg.Allg.Chem.|644|1057|doi:10.1002/zaac.201800269

Space GroupCrystallographybis(ferrocenyl(trimethylsilyl)amido)-tin(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 930539: Experimental Crystal Structure Determination

2016

Related Article: Nicholas Lease, Vadim Vasilevski, Monica Carreira, Andreia de Almeida, Mercedes Sanaú, Pipsa Hirva, Angela Casini, María Contel|2013|J.Med.Chem.|56|5806|doi:10.1021/jm4007615

Space GroupCrystallographydichloro-(2-(((diphenyl(ferrocenyl)phosphoranylidene)amino)methyl)pyridine)-palladium(ii) methanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1484852: Experimental Crystal Structure Determination

2016

Related Article: Torben Kienz, Christoph Förster, and Katja Heinze|2016|Organometallics|35|3681|doi:10.1021/acs.organomet.6b00619

Space GroupCrystallographyhexakis(mu-1-(ferrocenylimino)ethanethiolato)-hexa-silverCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1053708: Experimental Crystal Structure Determination

2015

Related Article: Jérôme Bayardon , Julie Bernard , Emmanuelle Rémond , Yoann Rousselin , Raluca Malacea-Kabbara , and Sylvain Jugé|2015|Org.Lett.|17|1216|doi:10.1021/acs.orglett.5b00167

Space GroupCrystallographylambda5-Boranyl(2-(dimesitylboryl)phenyl)ferrocenyl(phenyl)phosphoraneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 768533: Experimental Crystal Structure Determination

2010

Related Article: D.Siebler, C.Forster, T.Gasi, K.Heinze|2010|Chem.Commun.|46|4490|doi:10.1039/c0cc00227e

Space GroupCrystallographytetrakis(1'-methoxycarbonylferrocenyl)tinCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Inhibition of Cancer Derived Cell Lines Proliferation by Synthesized Hydroxylated Stilbenes and New Ferrocenyl-Stilbene Analogs. Comparison with Resv…

2014

Further advances in understanding the mechanism of action of resveratrol and its application require new analogs to identify the structural determinants for the cell proliferation inhibition potency. Therefore, we synthesized new trans-resveratrol derivatives by using the Wittig and Heck methods, thus modifying the hydroxylation and methoxylation patterns of the parent molecule. Moreover, we also synthesized new ferrocenylstilbene analogs by using an original protective group in the Wittig procedure. By performing cell proliferation assays we observed that the resveratrol derivatives show inhibition on the human colorectal tumor SW480 cell line. On the other hand, cell viability/cytotoxicit…

StereochemistryCell SurvivalPharmaceutical ScienceResveratrolresveratrolArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryIntestinal mucosaCell Line TumorDrug DiscoveryStilbenesresveratrol; methoxystilbenes; ferrocenylstilbene analogs; colon cancer; hepatoblastomaHumansViability assayFerrous CompoundsPhysical and Theoretical ChemistrymethoxystilbenesIntestinal MucosaCytotoxicityCell ProliferationCell growthferrocenylstilbene analogsOrganic ChemistryCell CycleEpithelial CellsHep G2 CellsCell cyclehepatoblastomaBiochemistrychemistrycolon cancerChemistry (miscellaneous)Cell cultureCancer cellMolecular MedicineColorectal NeoplasmsMolecules
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Performances of symmetrical achiral ferrocenylphosphine ligands in palladium-catalyzed cross-coupling reactions: A review of syntheses, catalytic app…

2007

Abstract Ferrocene derivatives bearing donor atoms led to the generation of several classes of metallo-ligands, which collectively show an impressive diversity of applications, especially in metal-catalyzed modern organic reactions. Based on the impetus provided by the use of the diphosphine 1,1′-bis(diphenylphosphino)ferrocene (dppf) the investigations directed towards the synthesis of new ferrocenylphosphines remain of fundamental and industrial interest. The present review aims to describe the performances in palladium-catalyzed cross-coupling reactions of symmetrical achiral ferrocenylphosphine ligands, mainly diphosphines. We specifically choose to restrict our review efforts to these …

Steric effectsferrocenylphosphine -palladiumSonogashira couplingBite angle010402 general chemistry01 natural sciencesCoupling reactionInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundcross-coupling reactionsDiphosphinesMaterials ChemistryOrganic chemistrystructurePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUScatalysis010405 organic chemistryNegishi coupling[CHIM.CATA]Chemical Sciences/CatalysisCombinatorial chemistry0104 chemical sciencesreactivityOrganic reactionFerrocenechemistryCoordination Chemistry Reviews
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