Zobrazeno 1 - 10 of 46 pro vyhledávání: '"J. B. Bremner"'
1
5-Substituted 3,4-dihydro-3-amino-2H-1-benzopyran derivatives: synthesis and interaction with serotoninergic receptors
Autor: B. Pfeiffer, René Misslin, P Delagrange, R. Rezaie, J. B. Bremner, G. Guillaumet, Pierre Renard, C Kopp, Benoît Joseph
Publikováno v: Journal of Pharmacy and Pharmacology. 53:959-968
A new series of 3,4-dihydro-3-amino-2H-1-benzopyran derivatives (1 and 2) bearing various substituents on the 5-position was successfully prepared via palladium-mediated cross-coupling reactions. Some of the new compounds showed high affinity for 5-H
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b4876db7ba779982f18061f1284f369
https://doi.org/10.1211/0022357011776388
Zobrazit plný text záznamu
2
ChemInform Abstract: Synthesis of the 3-Aza(9)metacyclophane System by Oxidative Cleavage of a 3-Aza(6)(1,7)naphthalenophane Derivative
Autor: W. Jaturonrusmee, J. B. Bremner
Publikováno v: ChemInform. 22
Reaction of 10,11-dimethoxy-1,4,5,6-tetrahydro-7,9-ethano-3-benzazecine-3(2H)- carbonitrile (3) with ozone at -78°, followed by destruction of the ozonide with dimethyl sulfide, gave, in 82% yield, 15-formyl-12,13-dimethoxy-8-oxo-4-azabicyclo[9.3.1]
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5c6095c4ca88c5e0e7cd8ac8bf133bda
https://doi.org/10.1002/chin.199117161
Zobrazit plný text záznamu
5
Modelling of adrenoceptor ligand targets based on novel medium- or macro-sized fused nitrogen heterocyclic systems
Autor: R, Griffith, J B, Bremner
Publikováno v: Journal of computer-aided molecular design. 13(1)
Novel medium- and macro-sized heterocyclic compounds were assessed for their potential as subtype-selective adrenergic ligands. Their conformational flexibilities were investigated and their geometric shapes were compared to rigid lead compounds of k
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c224289cfc1ca30924b827d13b1c095d
https://pubmed.ncbi.nlm.nih.gov/10087501
Zobrazit plný text záznamu
6
The action of 1,2,3,5,6,11b-hexahydro-[1]benzothieno [3,2-g]indolizine hydrochloride (ADT 16) on peripheral and central responses mediated by 5-hydroxytryptaminergic and adrenergic systems of the rat
Autor: I. M. Leitch, E. J. Browne, A. Rawlow, J. B. Bremner, R. G. King, A.L.A. Boura
Publikováno v: The Journal of pharmacy and pharmacology. 46(10)
Some acute pharmacological effects have been examined of racemic ADT 16 (1,2,3,5,6,11b-hexahydro[1]benzothieno[3,2-g]indolizine hydrochloride), on peripheral and central responses mediated by 5-HT and adrenergic systems in the rat. In-vitro, ADT 16(1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e5541b0d00e87faeed8a923059d446
https://pubmed.ncbi.nlm.nih.gov/7699570
Zobrazit plný text záznamu
7
Hepatotoxic constituents in the rumen of Brachiaria decumbens intoxicated sheep
Autor: A S, Abdullah, N H, Lajis, J B, Bremner, N W, Davies, W, Mustapha, M A, Rajion
Publikováno v: Veterinary and human toxicology. 34(2)
Spectroscopic examinations of purified extracts of the rumen content of sheep intoxicated by Brachiaria decumbens revealed the presence of a mixture of sapogenins, identified as 3-spirostanols. These isomeric steroid sapogenins (C27H44O3) are believe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ff761b93c131cc4c6641ef7df9ac6706
https://pubmed.ncbi.nlm.nih.gov/1509678
Zobrazit plný text záznamu
8
ChemInform Abstract: Manganese(III) Acetate-Induced Formation of a Fused, Chloro-Substituted β-Lactam Derivative from a Chloroacetamide
Autor: J. B. Bremner, W. Jaturonrusmee
Publikováno v: ChemInform. 21
Reaction of 1-chloroacetyl-5-methoxy-2,3-dihydro-1H-dibenzo[de,h]quinoline (1) with manganese(III) acetate in acetic acid at 50° gave the novel fused spiro derivative 11-chloro-4-methoxy-1,2-dihydro-6H-azeto[2,1-f]dibenzo[de,h]quinoline-6,12(11H)-di
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e09cf4471233153162eb8f455460b4fc
https://doi.org/10.1002/chin.199050209
Zobrazit plný text záznamu
9
ChemInform Abstract: Synthesis of Some Naphthothiadiazolophanes: Derivatives of 4,10,14-Ethenylylidene-7H-(1,2,3)thiadiazolo(5,4-e)azacyclotridecine and 4,11,15-Ethenylylidene(1,2,3)thiadiazolo(5,4-f)azacyclotetradecine
Autor: J. B. Bremner, W. Jaturonrusmee
Publikováno v: ChemInform. 21
Reaction of 7,8-dimethoxy-1,2,4,5,1lb, 11c-hexahydrobenzo [de]pyrrolo[3,2,1-ij][1,2,3]thiadiazolo[4,5-g]quinoline (3a) and 8,9-dimethoxy-2,3,5,6,12b,12c-hexahydro-1H-[1,2,3]thiadiazolo-[5',4':3,4]naphtho[2,1,8-ijalquinoline (3b) with cyanogen bromide
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6e17b469f70cef4abb621e749c77287d
https://doi.org/10.1002/chin.199013223
Zobrazit plný text záznamu
10
Synthesis of the 3-Aza[9]metacyclophane System by Oxidative Cleavage of a 3-Aza[6](1,7)naphthalenophane Derivative
Autor: J. B. Bremner, W. Jaturonrusmee
Publikováno v: Australian Journal of Chemistry. 44:135
Reaction of 10,11-dimethoxy-1,4,5,6-tetrahydro-7,9-ethano-3-benzazecine-3(2H)- carbonitrile (3) with ozone at -78°, followed by destruction of the ozonide with dimethyl sulfide, gave, in 82% yield, 15-formyl-12,13-dimethoxy-8-oxo-4-azabicyclo[9.3.1]
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4b3c8bf4dfdb51a2deb1620ef3450c3c
https://doi.org/10.1071/ch9910135
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje