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Results: 1-13 |
Results: 13
An expedient synthesis of 6-arylpiperidine-2,4-diones by chain-extension of beta-aryl-beta-aminoacids
Authors: Leflemme, N Dallemagne, P Rault, S
Citation: N. Leflemme et al., An expedient synthesis of 6-arylpiperidine-2,4-diones by chain-extension of beta-aryl-beta-aminoacids, TETRAHEDR L, 42(51), 2001, pp. 8997-8999
Synthesis and preliminary behavioural evaluation in mice of new 3-aryl-3-pyrrol-1-ylpropanamides, analogues of FGIN-1-27 and FGIN-1-43
Authors: Guillon, J Boulouard, M Lelong, V Dallemagne, P Rault, S Jarry, C
Citation: J. Guillon et al., Synthesis and preliminary behavioural evaluation in mice of new 3-aryl-3-pyrrol-1-ylpropanamides, analogues of FGIN-1-27 and FGIN-1-43, J PHARM PHA, 53(11), 2001, pp. 1561-1568
Synthesis of novel pyrazolopyrrolopyrazines, potential analogs of sildenafil
Authors: Kopp, M Lancelot, JC Dallemagne, P Rault, S
Citation: M. Kopp et al., Synthesis of novel pyrazolopyrrolopyrazines, potential analogs of sildenafil, J HETERO CH, 38(5), 2001, pp. 1045-1050
New aromatase inhibitors. Synthesis and biological activity of aryl-substituted pyrrolizine and indolizine derivatives
Authors: Sonnet, P Dallemagne, P Guillon, J Enguehard, C Stiebing, S Tanguy, J Bureau, R Rault, S Auvray, P Moslemi, S Sourdaine, P Seralini, GE
Citation: P. Sonnet et al., New aromatase inhibitors. Synthesis and biological activity of aryl-substituted pyrrolizine and indolizine derivatives, BIO MED CH, 8(5), 2000, pp. 945-955
Efficient synthesis of 2-aryl-6-methyl-2,3-dihydro-1H-pyridin-4-ones
Authors: Renault, O Guillon, J Dallemagne, P Rault, S
Citation: O. Renault et al., Efficient synthesis of 2-aryl-6-methyl-2,3-dihydro-1H-pyridin-4-ones, TETRAHEDR L, 41(5), 2000, pp. 681-683
Synthesis of new 2-(aminomethyl)-4-phenylpyrrolo[1,2-a]quinoxalines and their preliminary in-vivo central dopamine antagonist activity evaluation in mice
Authors: Guillon, J Boulouard, M Lisowski, V Stiebing, S Lelong, V Dallemagne, P Rault, S
Citation: J. Guillon et al., Synthesis of new 2-(aminomethyl)-4-phenylpyrrolo[1,2-a]quinoxalines and their preliminary in-vivo central dopamine antagonist activity evaluation in mice, J PHARM PHA, 52(11), 2000, pp. 1369-1375
New fused pyrazines. Synthesis of pyrido[3 ',2 ': 4,5]thieno[2,3-e]pyrrolo[1,2-a]pyrazine derivatives
Authors: El-Kashef, HS El-Dean, AMK Geies, AA Lancelot, JC Dallemagne, P Rault, S
Citation: Hs. El-kashef et al., New fused pyrazines. Synthesis of pyrido[3 ',2 ': 4,5]thieno[2,3-e]pyrrolo[1,2-a]pyrazine derivatives, J HETERO CH, 37(6), 2000, pp. 1521-1526
MR 20492 and MR 20494: two indolizinone derivatives that strongly inhibit human aromatase
Authors: Auvray, P Sourdaine, P Moslemi, S Seralini, GE Sonnet, P Enguehard, C Guillon, J Dallemagne, P Bureau, R Rault, S
Citation: P. Auvray et al., MR 20492 and MR 20494: two indolizinone derivatives that strongly inhibit human aromatase, J STEROID B, 70(1-3), 1999, pp. 59-71
First synthesis of isothianinhydrin, the second thiophene isostere of ninhydrin
Authors: Khanh, LP Dallemagne, P Rault, S
Citation: Lp. Khanh et al., First synthesis of isothianinhydrin, the second thiophene isostere of ninhydrin, SYNLETT, (9), 1999, pp. 1450-1452
First synthesis of 1-phenyl-3-pyrrol-1-ylindan-2-carboxylic acid, a new scaffold of potential non-peptide endothelin receptor antagonists
Authors: Guillon, J Dallemagne, P Stiebing, S Bovy, PR Rault, S
Citation: J. Guillon et al., First synthesis of 1-phenyl-3-pyrrol-1-ylindan-2-carboxylic acid, a new scaffold of potential non-peptide endothelin receptor antagonists, SYNLETT, (8), 1999, pp. 1263-1264
Synthesis of new phenylpyrrolizinones via a Mannich reaction
Authors: Sonnet, P Miel, H Guillon, J Dallemagne, P Rault, S
Citation: P. Sonnet et al., Synthesis of new phenylpyrrolizinones via a Mannich reaction, HETEROCYC C, 5(1), 1999, pp. 25-26
Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: a general and flexible route to 3-arylindazoles
Authors: Collot, V Dallemagne, P Bovy, PR Rault, S
Citation: V. Collot et al., Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: a general and flexible route to 3-arylindazoles, TETRAHEDRON, 55(22), 1999, pp. 6917-6922
Friedel-Crafts acylation with malonic acids in polyphosphoric acid
Authors: Renault, O Dallemagne, P Rault, S
Citation: O. Renault et al., Friedel-Crafts acylation with malonic acids in polyphosphoric acid, ORG PREP PR, 31(3), 1999, pp. 324-328
Risultati: 1-13 |