Hauptinhalt
Topinformationen
Publikationen 2010
Viologen-based benzylic dendimers: selective synthesis of 3,5-bis(hydroxy-methyl) benzylbromide and conformational analysis of the corresponding viologen dendrimer subunit
Kathiresan, M., Walder, L., Ye, F. and Reuter, H.
Tetrahedron Letters. 2010, 51, 2188-2192.
2-Amino-8-(2-deoxy-2-fluoro-ß-D-arabinofuranosyl)imidazo[1,2-a][1,3,5]-triazin-4[8H]-one monohydrate, a 2′-deoxyguanosine analoque with an altered Watson-Crick recognition site
Jiang, D., Budrow, S., Glacon, V., Eickmeier H., Reuter, H., He, Y and Seela, F.
Acta Cryst. 2010, C66, o194-o197.
(E)-4-(2,3-Dihydro-1,3-benzothiazol-2-ylidene)-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one
Chakibe, I., Zerzouf, A., Essassi E.-M., Reichelt, M. and Reuter, H.
Acta Cryst. 2010, E66, o1096.
Monoorganotin-polyoxometal-compounds. Part IV: Na2[(iPrSn)3(OV)4O10(OH)3] × 5H2O × 3DMSO, a novel branched tetravanadate(V) stabilized by a trimeric monoorganotin-oxo-hydroxo unit
Reuter, H. and Izaaryene, M.
Inorg. Chim. Acta 2010, E66, m1265.
Et2SnCl2 × H2O and the trigonal-biypramidal transition state of a SN2 reaction.
Ye, F. and Reuter, H.
Phosphorus, Sulfur and Silicon 2011, 186, 1367-1369.
[(iPrSn)12O14(OH)6][(iPrSn)3(OV)4O10(OH)3] × 4DMSO: Evidence for the formation of contact ion pairs resulting from the nucleophilic attack on a square pyramidally coordinated tin atom
Izaaryene, M. and Reuter, H.
Phosphorus, Sulfur and Silicon 2011, 186, 1364-1366.
Disodium 4,5,6-trihydroxybenzene-1,3-disulfonate dihydrate
Song, E., Podschun, J., Wilberts, H., Beginn, U. and Reuter, H.
Acta Cryst. 2010, E66, m1265.
7-Amino-1-(3-deoxy-ß-erythro-pentofuranosyl)-1H-1,2,3-triazolo-[4,5-d]pyrimidine: an 8-azaadenine nucleoside with the nucleobase in a syn conformation
Jiang, D., He, Y., Budow, S., Kazimierczuk, Z., Reuter, H. and Eickmeier, H.
Acta Cryst. 2010, E66, o561-o564.
Etude de la condensation du 2-aminothiophenol avec l'acetylacetate d'ethyle
Baryala, Y., Zerzouf, A., Salem, M., Essassi, E.M., Reuter, H.
J. Mar. Chim. Heterocycl. 2010, 9, 26-35.
