Zobrazeno 1 - 10
of 37
pro vyhledávání: '"V. Askam"'
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 20:1331-1338
A new route for preparing aminoglutethimide labelled at C5 (Scheme I (10)) with 14C is described, which offers the advantage of introducing 14C at a late stage in the synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51cc64335c8251b96389fa50ceeb16ce
https://doi.org/10.1002/jlcr.2580201204
https://doi.org/10.1002/jlcr.2580201204
Autor:
G. Peter Briner, Joseph Miller, H. R. Arthur, W. H. Hui, G. Baddeley, P. G. Nield, D. J. A. Dear, D. D. Eley, R. J. W. Le Fèvre, J. B. Sousa, R. L. Werner, C. M. French, D. Harrison, W. J. Adams, D. K. Patel, V. Petrow, H. Seaman, P. J. Taylor, William A. Waters, V. Askam, W. H. Linnell, John Frederick Grove, A. A. Woolf, E. E. Aynsley, G. Hetherington, W. Lawson, D. A. Everest, N. Greenhalgh, P. A. J. Gorin, L. Hough, J. K. N. Jones, J. F. Cavalla, A. G. Maddock, F. Pinto Coelho, E. G. E. Hawkins, W. E. Nelson
Publikováno v:
J. Chem. Soc.. :4682-4705
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2461a37ed9e175a821f0857b4f0f08fa
https://doi.org/10.1039/jr9540004682
https://doi.org/10.1039/jr9540004682
Publikováno v:
Journal of Pharmacy and Pharmacology. 8:318-322
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc76f9abbd37b5ab68a8fc8c8ff5112
https://doi.org/10.1111/j.2042-7158.1956.tb12162.x
https://doi.org/10.1111/j.2042-7158.1956.tb12162.x
Publikováno v:
J. Chem. Soc. C. :1524-1526
Diels–Alder reaction of 1,2-dihydro-6,7-dimethoxy-4-vinylnaphthalene (1) and 2-methylenecyclohexanone (2), generated from a Mannich base, gave 1,2,3,9,10a-hexahydro-6,7-dimethoxyphenanthrene-2-spirocyclohexan-2′-one (3a) as two diastereoisomers:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c7d12f5d09a815cd45cbca18a0dbbb7
https://doi.org/10.1039/j39710001524
https://doi.org/10.1039/j39710001524
Autor:
V. ASKAM, T. U. QAZI
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4af7f0ce169ba80eeacea7c1997eec4e
https://doi.org/10.1002/chin.197737165
https://doi.org/10.1002/chin.197737165
Publikováno v:
The Journal of pharmacy and pharmacology. 18(3)
Methyl 11-oxo-18 β-A-neo-oleana-3, 12-dien-30-oate and the corresponding 18α-isomer have been prepared and tested for anti-inflammatory and antidiuretic activity. Relative to methyl glycyrrhetinate, both kinds of activity and toxicity are reduced b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca5928f8e727535edd17e19a540c20a
https://pubmed.ncbi.nlm.nih.gov/4163701
https://pubmed.ncbi.nlm.nih.gov/4163701
Autor:
D. M. Bradley, V. Askam
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7f41f93facc4068be76b796fda48fca
https://doi.org/10.1002/chin.197134265
https://doi.org/10.1002/chin.197134265
Autor:
V. Askam, R. H. L. Deeks
Publikováno v:
Journal of the Chemical Society. Perkin transactions 1. 14
When 3-nitro-o-xylene was oxidised with chromyl acetate, the methyl group remote from the nitro-group was attacked, yielding 2-methyl-3-nitrobenzylidene diacetate. The adjacent methyl group reacted with diethyl oxalate under the conditions of the Cla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d67fbfe7273b29592c1d95b2dd4e1c
https://pubmed.ncbi.nlm.nih.gov/5817990
https://pubmed.ncbi.nlm.nih.gov/5817990
Autor:
V. Askam, R. H. L. Deeks
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Durch Alkylierung von 2-Morpholino-inden in DMF mit entsprechenden Bromalkylcarbonsaureathylestern, gefolgt von HC1-Hydrolyse [ein Uberschus an HCl bewirkt bei der Darstellung von (Ib) die Bildung des Lactons (IV) als Hauptprodukt], werden die Indano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7646dcd6e662df059430be918104c677
https://doi.org/10.1002/chin.197101361
https://doi.org/10.1002/chin.197101361
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d391f6037e09e7e7f225cf9d3a995fc
https://doi.org/10.1002/chin.197129213
https://doi.org/10.1002/chin.197129213