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Comparative Effectiveness of Cladribine and S1P Receptor Modulators in Treatment-Naive Relapsing-Remitting MS.

JAMA Netw Open
Haggiag S, Prosperini L, Filippi M, Rocca MA, Iaffaldano P, Patti F, Inglese M, Borriello G, Totaro R, Lus G, Fantozzi R, Brescia Morra V, Romano S, Frau J, Marfia GA, Maniscalco GT, Amato MP, Di Sapio A, De Luca G, Crisafulli SG, Curti E, Foschi M, Cavalla P, Salemi G, Conte A, Valentino P, Ferraro D, Lugaresi A, Realmuto S, Perini P, Ferraro E, Montepietra S, Avolio C, Vianello M, Gazzola P, Marinelli F, Pasquali L, Bucello S, Vecchio D, Protti A, Sangalli F, Rovaris M, Grimaldi L, De Riz M, Barone P, Scarano V, Ardito B, Sinisi L, Immovilli P, Pesci I, Colombo E, Capobianco MA, Fioretti C, Coniglio MG, Giordano A, Tassinari T, Cargnelutti D, Matta F, Falcini M, Gatto M, Mascoli N, Balgera R, Sessa E, Iodice R, Solaro C, Plewnia K, Santangelo M, Barcella V, Ferrò MT, Sica F, Cerqua R, Santuccio G, Corea F, Leone A, Nasuelli D, Rini AM, Brichetto G, Cottone S, Ulivelli M, Pizzorno M, Rossi P, Milano E, Zuliani L, Ruggieri S, Gasperini C, Trojano M, Tortorella C.   +86 more
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Polymers with indan units

Macromolecular Symposia, 1995
AbstractCationic polymerisation of 1, 4‐diisopropenyl benzene, 1, 4‐(2‐chloro‐isopropyl)benzene and related compounds yields soluble polymers with repeating units of indan.High performance polymers with indan units are available via nucleophilic substitution of halogenated aromatic monomers containing a central indan element, which are synthesized from
Oskar Nuyken, Gerhard Maier, Michael Leitner, Dazhong Yang, Martin Wolf   +4 more
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NEW CARBOCYCLIC NUCLEOSIDES DERIVED FROM INDAN

Nucleosides, Nucleotides and Nucleic Acids, 2001
Seven new carbocyclic nucleosides derived from indan (1a-g) were efficiently prepared from 1,2-indanedimethanol vía Mitsunobu reaction with 6-chloroadenine and subsequent introduction of the appropriate substituent.
F, Abad, F, Alvarez, F, Fernández, X, García-Mera, J E, Rodríguez-Borges   +4 more
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2-(2-Thiazolylhydrazono)indan-1,3-dione

Acta Crystallographica Section C Crystal Structure Communications, 1997
The structural results clearly indicate that 2-(2-thiazolylhydrazono)indan-1,3-dione, C12H7N3O2S, exists as a keto-hydrazone tautomer in the solid state. The indandione and thiazolylhydrazone groups are connected by a C=N bond and the H atom bonded to N1 refines with a normal temperature factor. The entire molecule is essentially planar.
Ozgun, BH, Ozbey, S, Ertan, N, Temel, A
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2-Spiro-indan-1,3-dione

Monatshefte f�r Chemie, 1981
The reaction of 1,3-indandione, formaldehyde and primary amines does not gives doubleMannich bases as described in literature, but the title compounds.
Hans M�hrle, Sigrid D�rnbrack, Hans-Joachim Novak   +2 more
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Heteropolyalanes, ‐Gallanes, ‐Indanes, and ‐Thallanes

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Werner Uhl, Herbert W. Roesky
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Vapor-pressure and enthalpy of vaporization of indan and five methyl-substituted indans

The Journal of Chemical Thermodynamics, 1978
Abstract Vapor-pressure determinations were made for indan, 1,1-dimethylindan, 4,6-dimethylindan, 4,7-dimethylindan, 1,1,4,6-tetramethylindan, and 1,1,4,7-tetramethylindan. The results were used to obtain derived values of enthalpy of vaporization.
A.G. Osborn, D.W. Scott
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Spiro-indans from Cannabis sativa

Phytochemistry, 1986
Abstract Three new spiro-indans were isolated from hashish (Cannabis sativa). Their chemical structures were established by spectroscopic means, and by chemical correlation with cannabispiran and iso-cannabispiran. They were found to be 7-hydroxy-5-methoxyindan-1-spiro-cyclohexane, its isomer 5-hydroxy-7-methoxyindan-1-spirocyclo-hexane and 5,7 ...
Farouk S. El-Feraly, Moshera M. El-Sherei, Farid J. Al-Muhtadi   +2 more
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Polyketones containing indane structure elements

Polymer Bulletin, 1992
Polyketones with indane structure elements were prepared by Friedel-Crafts polycondensation in three different reaction media. Only oligomers or insoluble material could be obtained, probably due to a side reaction of the indane ring, which leads to crosslinking at high conversion.
Gerhard Maier, Dazhong Yang, Oskar Nuyken   +2 more
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Indan-2,2-dicarboxylic acid, C11H10O4

Acta Crystallographica Section C Crystal Structure Communications, 1994
The cyclopentene ring has an envelope conformation with the C atom carrying the carboxyl group lying 0.355 (2) A out of the best plane of the other four C atoms. The cyclopentene torsion angle along the fusion of both rings has a magnitude of -2.5 (3) o .
J. G. Garcia, J. D. Enas, F. R. Fronczek
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