Search results for "Nap"

showing 10 items of 2226 documents

CCDC 1428734: Experimental Crystal Structure Determination

2015

Related Article: Nora M. Kaluza, Dieter Schollmeyer, Udo Nubbemeyer|2016|Eur.J.Org.Chem.|2016|357|doi:10.1002/ejoc.201501341

(RR)-2-(6-((t-butyl(dimethyl)silyl)oxy)-2-methylhex-1-en-3-yl)-6-methoxy-34-dihydronaphthalen-1(2H)-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 250963: Experimental Crystal Structure Determination

2005

Related Article: J.F.Schneider, M.Nieger, K.Nattinen, B.Lewall, E.Niecke, K.H.Dotz|2005|Eur.J.Org.Chem.|2005|1541|doi:10.1002/ejoc.200400800

(RS)-1013-Dibromo-44-di-t-butyl-dinaphtho(21-d:1'2'-f)(132)-dioxasilepinSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 173987: Experimental Crystal Structure Determination

2003

Related Article: K.H.Dotz, N.Szesni, M.Nieger, K.Nattinen|2003|J.Organomet.Chem.|671|58|doi:10.1016/S0022-328X(03)00045-7

(RS)-Tricarbonyl-(eta^6^-1-(t-butyl(dimethyl)siloxy)-2-(trimethylsilyl)-4-methoxynaphthalene)-chromium(0)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 261600: Experimental Crystal Structure Determination

2005

Related Article: F.Lauterwasser, M.Nieger, H.Mansikkamaki, K.Nattinen, S.Brase|2005|Chem.-Eur.J.|11|4509|doi:10.1002/chem.200500146

(RpS)-5-(1-(1'-(2-naphthyl)ethylimino)ethyl)-4-hydroxy(2.2)paracyclophaneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 941095: Experimental Crystal Structure Determination

2013

Related Article: Christoph Gütz, Rainer Hovorka, Caroline Stobe, Niklas Struch, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Org.Chem.|2014|206|doi:10.1002/ejoc.201301314

(mu2-(M)-44'-((22'-bis(Methoxymethoxy)-11'-binaphthalene-66'-diyl)diethyne-21-diyl)dipyridine)-(mu2-(P)-44'-((22'-bis(methoxymethoxy)-11'-binaphthalene-66'-diyl)diethyne-21-diyl)dipyridine)-bis(13-bis(diphenylphosphino)propane)-di-palladium(ii) tetrakis(trifluoromethanesulfonate) tetrahydropyran solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Due note etimologiche circostanziali circa il Ms.II.D.54 (BNN) attribuito a Baffi

2019

Within the investigations on the attribution of some manuscripts to the famous philologist P. Baffi and now kept at the National Library of Naples (BNN), this brief contribution investigates in detail some of the passages contained in Ms.II.D.54 (f. 234r et f. 325r), in order to understand its meaning and to evaluate and validate its attributing hypotheses.

//pages.uv.es/SPhV/cas/numero21.wiki [Etymological notes ? Baffi ? Ms.II.D.54 (BNN) 5 21 https]UNESCO::CIENCIAS DE LAS ARTES Y LAS LETRASin order to understand its meaning and to evaluate and validate its attributing hypotheses. Note etimologiche ? Baffi ? Ms.II.D.54 (BNN)this brief contribution investigates in detail some of the passages contained in Ms.II.D.54 (f. 234r et f. 325r):CIENCIAS DE LAS ARTES Y LAS LETRAS [UNESCO]Nikola Within the investigations on the attribution of some manuscripts to the famous philologist P. Baffi and now kept at the National Library of Naples (BNN)Etymological notes ? Baffi ? Ms.II.D.54 (BNN) 5 21 https://pages.uv.es/SPhV/cas/numero21.wiki1135-9560 8276 Studia philologica valentina 536436 2019 21 7225810 Due note etimologiche circostanziali circa il Ms.II.D.54 (BNN) attribuito a Baffi Bellucci
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Enantioselective synthesis of 4H-pyranonaphthoquinones via sequential squaramide and silver catalysis

2015

Chemical communications 52(8), 1669-1672(2016). doi:10.1039/C5CC09592A

010402 general chemistry01 natural sciencescatalystsCatalysisCatalysisMichael additionMaterials ChemistryOrganic chemistryenantioselective synthesista116Hydroalkoxylation010405 organic chemistryChemistryMetals and AlloysSquaramideEnantioselective synthesisGeneral Chemistry540hydroalkoxylation0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialspyranonaphthoquinonesddc:540Ceramics and CompositesMichael reactionChemical Communications
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Practical Syntheses of Terrylene Chromophores from Naphthalene and Perylene Building Blocks

2017

A facile and efficient method to synthesize terrylene imides, a unique class of chromophores, and their derivatives from commercially available naphthalene and perylene building blocks is reported. We developed an extremely efficient Suzuki/C-H-arylation coupling cascade with Pd2(dba)3/PCy3 (dba = dibenzylidenacetone, Cy = cyclohexyl) as the catalyst and highly soluble naphthalene derivatives as starting materials. This efficiency allows purification via precipitation and crystallization, avoiding time-consuming column chromatography. For the first time, the highly soluble 3,4,11,12-terrylene tetraester was prepared in gram scale with yields up to 75 % which thus becomes a versatile startin…

010405 organic chemistryChemistryGeneral ChemistryChromophore010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionCatalysischemistry.chemical_compoundColumn chromatographylawOrganic chemistryCrystallizationPeryleneNaphthaleneAdvanced Synthesis & Catalysis
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Synthesis of 1,3-bis(trimethylcyclam) and 1,3-bis(trimethylcyclen) substituted benzenes

2009

Pd-catalyzed amination of 1,3-dibromobenzene with N,N',N''-trimethylcyclam and N,N',N''-trimethylcyclen provided corresponding 1,3-bis(tetraazamacrocyclic) derivatives of benzene in 25-32% yields. The dependence of the products yields on the phosphine ligand applied (BINAP, DavePHOS) as well as on the stoichiometry of starting compounds was established. Scope and limitations for the synthesis of N-phenyl and N-(3-bromophenyl) derivatives of trimethylcyclam and trimethylcyclen were demonstrated.

010405 organic chemistryLigandPd catalysis[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistryamination[CHIM.ORGA] Chemical Sciences/Organic chemistry010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical Chemistryaryl halideschemistry.chemical_compoundchemistrytetraazamacrocycles[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryBenzenePhosphineStoichiometryAminationComputingMilieux_MISCELLANEOUSBINAP
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6-Polyamino-substituted quinolines: synthesis and multiple metal (CuII, HgIIand ZnII) monitoring in aqueous media

2019

Chemoselective palladium-catalyzed arylation of polyamines with 6-bromoquinoline has been explored to prepare chelators for the detection of metal cations in aqueous media. The introduction of a single aromatic moiety into non-protected polyamine molecules was achieved using the commercially available Pd(dba)2/BINAP precatalyst to afford nitrogen chelators, in which the aromatic signalling unit is directly attached to the polyamine residue. Water-soluble receptors were then synthesized using N-alkylation of these polyamines by hydrophilic coordinating residues. By combining rich photophysical properties of the 6-aminoquinoline unit with a high coordination affinity of chelating polyamines a…

010405 organic chemistryMetal ions in aqueous solutionOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistryFluorescence0104 chemical sciencesMetalchemistry.chemical_compoundResidue (chemistry)chemistryvisual_artvisual_art.visual_art_mediumMoleculeChelationPhysical and Theoretical ChemistryPolyamineBINAPOrganic & Biomolecular Chemistry
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