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Supramolecular Recognition of a DNA Four-Way Junction by an M<sub>2</sub>L<sub>4</sub> Metallo-Cage, Inspired by a Simulation-Guided Design Approach. [PDF]
Dettmer SJ +7 more
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The Journal of Organic Chemistry, 2014
Fifteen substituted maleimide cycloadducts of anthracene derivatives were synthesized in one or two steps from available precursors in yields ranging from 32 to 63%. They differ in the nature of the group on the maleimide nitrogen atom and of the substituents on the anthracene platform.
Ek Raj, Thapaliya +2 more
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Fifteen substituted maleimide cycloadducts of anthracene derivatives were synthesized in one or two steps from available precursors in yields ranging from 32 to 63%. They differ in the nature of the group on the maleimide nitrogen atom and of the substituents on the anthracene platform.
Ek Raj, Thapaliya +2 more
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Diels–Alder reactions of anthracene, 9-substituted anthracenes and 9,10-disubstituted anthracenes
Tetrahedron, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Atherton JCC, Jones S
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Photoionization of anthracene and anthracene derivatives
Journal of Photochemistry and Photobiology A: Chemistry, 1999Anthracene (III) and the derivatives 9-methoxymethylanthracene (IV), 9-cyanoanthracene (V) and (E-3-phenyl-prop-2-ene-1-yl(anthracene-9-methyl)-ether) (I) were subjected to irradiation at inca347 nm in dilute deoxygenated acetonitrile solution at room temperature.
C. Zimmermann +4 more
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ChemInform Abstract: ANTHRACEN‐CYANAT UND ANTHRACEN‐OXAZINONE
Chemischer Informationsdienst. Organische Chemie, 1970AbstractDas aus dem Hydroxy‐anthracen (I) und BrCN in Aceton in Gegenwart von Triäthylamin dargestellte Cyanat (II) gibt in saurer, wäßriger Lösung das Carbamat (III), mit H2S das Thiocarbamat (IV).
MIR HEDAYATULLAH +2 more
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Acta Crystallographica Section C Crystal Structure Communications, 1997
Anthracene-9-carboxylic acid, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic-dimer type about a center of symmetry. The carboxyl O atoms are ordered, as is the carboxyl H atom. The anthracene core is almost planar and shows good agreement with the anthracene core of anthracene-1, 8 ...
L J, Fitzgerald, R E, Gerkin
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Anthracene-9-carboxylic acid, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic-dimer type about a center of symmetry. The carboxyl O atoms are ordered, as is the carboxyl H atom. The anthracene core is almost planar and shows good agreement with the anthracene core of anthracene-1, 8 ...
L J, Fitzgerald, R E, Gerkin
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Acta Crystallographica Section C Crystal Structure Communications, 1997
The title compound, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic dimer type about a center of symmetry. The carboxyl O atoms are ordered as is the carboxyl H atom. The anthracene core, while less nearly planar, shows good agreement with the anthracene cores of anthracene-9 ...
L J, Fitzgerald, R E, Gerkin
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The title compound, C15H10O2, was found to crystallize in the centrosymmetric space group P2(1)/n. The hydrogen bonding is of the cyclic dimer type about a center of symmetry. The carboxyl O atoms are ordered as is the carboxyl H atom. The anthracene core, while less nearly planar, shows good agreement with the anthracene cores of anthracene-9 ...
L J, Fitzgerald, R E, Gerkin
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Anthracene and Anthracene-Tetracene Crystals from Vapor
Molecular Crystals, 1968Abstract Molecular crystals in general are receiving increased attention and anthracene crystals in particular are in demand for use in various studies. Consequently, several techniques have been developed for growing anthracene crystals–most of which have involved growth from the melt.1–3 In those common method is to use a cooled collector plate.3,4 ...
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