Zobrazeno 1 - 10
of 120
pro vyhledávání: '"G M, Shutske"'
Autor:
J. D. Iv Tomer, G. M. Shutske
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::610cf656ad7b7462ded279af644857f3
https://doi.org/10.1002/chin.199333178
https://doi.org/10.1002/chin.199333178
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66cd7cef10ec838b43fdefa235cc1d3e
https://doi.org/10.1002/chin.199819174
https://doi.org/10.1002/chin.199819174
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 18(5)
Tacrine (THA) is a potent cholinesterase inhibitor being studied for the treatment of Alzheimer's disease. The metabolism and excretion of THA were studied in rats following a single oral dose of 20 mg/kg of THA. The results show THA was extensively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef84c395dd8bb8dd9469f7bb4f3a2820
https://pubmed.ncbi.nlm.nih.gov/1981736
https://pubmed.ncbi.nlm.nih.gov/1981736
Autor:
G. M. Shutske, E. Campaigne
Publikováno v:
Journal of Heterocyclic Chemistry. 12:67-74
By a combination of hydrolysis, decarboxylation, and methylation diethyl 1-methyl-3-hydroxy-5-phenylpyrrole-2,4-dicarboxylate was converted into 1-methyl-3-methoxy-5-phenyl-pyrrole-2,4-dicarboxylic acid (5) and into the isomeric compounds ethyl 1-met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f826dffa48f6103f7a86773c7e4396e9
https://doi.org/10.1002/jhet.5570120111
https://doi.org/10.1002/jhet.5570120111
Autor:
E. Campaigne, G. M. Shutske
Publikováno v:
Journal of Heterocyclic Chemistry. 11:929-936
Diethyl 1-methyl-3-hydroxy-5-phenylpyrrole-2,4-dicarboxylate has been synthesized in good yield from readily available materials, diethyl benzylidenemalonate and ethyl sarcosinate. It was found to react with oxygen in aqueous base to give two oxidati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df5e99ace943e163268df0bcbd02d0d6
https://doi.org/10.1002/jhet.5570110614
https://doi.org/10.1002/jhet.5570110614
Autor:
E. Campaigne, G. M. Shutske
Publikováno v:
Journal of Heterocyclic Chemistry. 13:497-503
Three new dipyrromethenes have been synthesized as analogs of prodigiosin: 3-methoxy-5-phenyl-2,2′-dipyrromethene (10a), 3-methoxy-4 -pentyl-5-phenyl-5′-methyl-2,2′-dipyrromethene (10b), and 3-methoxy-4′-pentyl-5′-methyl-5-(2″-thienyl)-2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ae2bb8ecfe9eb5cb42e8d1f83cc5604
https://doi.org/10.1002/jhet.5570130315
https://doi.org/10.1002/jhet.5570130315
Autor:
Escorihuela, Jorge1 (AUTHOR) jorge.escorihuela@uv.es, Fustero, Santos1 (AUTHOR) santos.fustero@uv.es
Publikováno v:
Chemical Record. Sep2023, Vol. 23 Issue 9, p1-25. 25p.
Autor:
Jung, Min‐Jung1 (AUTHOR), Paladhi, Sushovan1,2 (AUTHOR), Song, Choong Eui1 (AUTHOR) s1673@skku.edu
Publikováno v:
Bulletin of the Korean Chemical Society. May2023, Vol. 44 Issue 5, p420-424. 5p.
Publikováno v:
Journal of Heterocyclic Chemistry. 14:329-331
Ethyl sarcosinate adds to 2, −3- and 4-pyridylmethylidenemalonates to produce the Michael adducts, which can be conveniently cyclized to oxopyrrolidine diesters under Dieckmann conditions. Mild oxidation converted the crude adducts to the isomeric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03b5815dd61d219aae8900b0f6110890
https://doi.org/10.1002/jhet.5570140235
https://doi.org/10.1002/jhet.5570140235
Autor:
G. M. Shutske, E. Campaigne
Publikováno v:
Journal of Heterocyclic Chemistry. 12:317-319
Three new rnethoxypyrrole esters, ethyl 1-methyl-3-methoxy-5-phenylpyrrole-2-earboxylate, diethyl l-methyl-3-methoxy-5-phenylpyrrole-2,4-diearboxylate, and ethyl l-methyl-2-phenyl-4-methoxypyrrole-3-carboxylate were reduced with diborane/tetrahydrofu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce53c067864e7107bb752234d4dfd4d2
https://doi.org/10.1002/jhet.5570120221
https://doi.org/10.1002/jhet.5570120221