Institution
Roussel Uclaf
About: Roussel Uclaf is a based out in . It is known for research contribution in the topics: Alkyl & Alkoxy group. The organization has 1888 authors who have published 2338 publications receiving 36508 citations.
Topics: Alkyl, Alkoxy group, Aryl, Carbon, Carboxylic acid
Papers published on a yearly basis
Papers
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08 Apr 1993TL;DR: The application relates to the products (I): in which: - R represents H, halogen or alkyl which is linear, branched or cyclic, optionally interrupted by one or a number of O, S or N, or R represents optionally substituted aryl or heterocyclic aryls with p = 0 to 6 as mentioned in this paper.
Abstract: The application relates to the products (I): in which: - R represents H, halogen or alkyl which is linear, branched or cyclic, optionally interrupted by one or a number of O, S or N, or R represents optionally substituted aryl, aryloxy or heterocyclic aryl or with p = 0 to 6, or R represents with Ra, Rb and Rc = alkyl or R represents with a and b = H, halogen, OH, alkyl or alkoxy or a and b together form a cycloalkyl and R' has one of the values of R, - R2 and R3 represent H, alkyl or to their process of preparation and to their application as pesticidal agent.
5 citations
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27 Jun 1979TL;DR: In this paper, the Δ4 -androstenes of the formula ##STR1## were considered and the dotted lines in the A and B rings indicated the optional presence of one or two double bonds in the 1(2) and 6(7)-positions with the proviso that when R1 is methyl, R2 is saturated or unsaturated alkyl and the B ring is saturated, Y is methyl having anti-inflammatory activity and novel intermediates.
Abstract: Novel Δ4 -androstenes of the formula ##STR1## wherein R1 is alkyl of 1 to 3 carbon atoms, Y is selected from the group consisting of hydrogen, fluorine and methyl, R2 is selected from the group consisting of saturated and unsaturated alkyl of 1 to 12 carbon atoms, --CF3, aryl of 6 to 12 carbon atoms and aralkyl of 7 to 12 carbon atoms and the dotted lines in the A and B rings indicate the optional presence of one or two double bonds in the 1(2) and 6(7)-positions with the proviso that when R1 is methyl, R2 is saturated or unsaturated alkyl and the B ring is saturated, Y is methyl having anti-inflammatory activity and novel intermediates.
5 citations
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22 Apr 19645 citations
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TL;DR: The present results show that the alpha 2-adrenergic antagonist RU 52583 possesses cognition-enhancing properties in rats with damage to the septohippocampal system.
Abstract: The anti-amnesic action of RU 52583, an alpha 2-adrenergic receptor antagonist, was evaluated through performance of spatial tasks in a radial maze by rats with N-methyl-D-aspartic acid (NMDA) lesion of the medial septal (MS) nuclei. Memory performance of lesioned or sham-operated rats was evaluated by measuring reference memory as long-term maintenance of an acquired performance and working memory or memory for recent events. The lesion: a produced significant impairments of the animals' memory performance, b) significantly reduced the sodium-dependent high-affinity choline uptake in the hippocampal formation, and c) deeply disrupted cholinergic hippocampal theta waves. Oral administration of RU 52583 at 1 and 2 mg/kg (tested doses: 1-5 mg/kg) prior to performance of the task markedly reduced memory impairments, whereas idazoxan, another alpha 2-adrenergic receptor antagonist, had no effect at tested doses (2-5 mg/kg). Cholinergic drugs--arecoline at 0.1 and 1 mg/kg (tested doses: 0.05-1 mg/kg) and physostigmine at 0.02 and 0.1 mg/kg (tested doses: 1, 2, and 5 mg/kg)-administered intraperitoneally showed a tendency to alleviate memory deficits. The present results show that the alpha 2-adrenergic antagonist RU 52583 possesses cognition-enhancing properties in rats with damage to the septohippocampal system.
5 citations
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08 Jan 1982TL;DR: In this article, a process for the preparation of products of formula: in which: R1 = H, Alk C1-4 optionally substituted Alkenyl or alkynyl C2-4 R2 = Alk A, B, C, D optionally bear one or more double bonds and are optionally substituted, starting from products comprising at 17 a radical: R3 =H, protective group, by the action of an acetoxylation agent, then of a hydrolysis agent and finally a deacetoxylating agent.
Abstract: The present application relates to a process for the preparation of products of formula: in which: R1 = H, Alk C1-4 optionally substituted Alkenyl or alkynyl C2-4 R2 = Alk C1-4 A, B, C, D optionally bear one or more double bonds and are optionally substituted, starting from products comprising at 17 a radical: R3 = H, protective group, by the action of an acetoxylation agent, then of a hydrolysis agent and finally a deacetoxylation agent.
5 citations
Authors
Showing all 1888 results
Name | H-index | Papers | Citations |
---|---|---|---|
Fernand Labrie | 110 | 885 | 48308 |
Lionel H. Opie | 84 | 519 | 25964 |
Alain Bélanger | 70 | 244 | 16469 |
Michel J. Tremblay | 53 | 273 | 10485 |
Pierre Monsan | 51 | 216 | 8049 |
Samir Z. Zard | 50 | 575 | 10739 |
Alejandro Aruffo | 47 | 123 | 14084 |
Samuel S.C. Yen | 47 | 96 | 6865 |
Dominique Maraninchi | 47 | 188 | 8108 |
Serge Erlinger | 46 | 152 | 8200 |
Romain Lefebvre | 40 | 221 | 5269 |
William B. Motherwell | 39 | 305 | 6357 |
Jean-Pierre Raynaud | 38 | 104 | 5075 |
André Lemay | 38 | 114 | 4264 |
Patrick J. Creaven | 32 | 102 | 3435 |