Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Robert E. Gilman"'
Publikováno v:
The Journal of Infectious Diseases. 183:1308-1309
Autor:
Robert E. Gilman, Léo Marion
Publikováno v:
Canadian Journal of Chemistry. 42:2700-2704
The alkaloid indaconitine has been converted into delphinine by replacement of a secondary hydroxyl by hydrogen and substitution of an imino-methyl for the imino-ethyl group originally present. This correlation rigorously establishes the structure of
Publikováno v:
Journal of Chromatography A. 44:563-568
Ten cycloketone 2,4-dinitrophenylhydrazones have been chromatographed by thin-layer techniques using Eastman Chromagram sheets coated with silica gel and developed with benzene in Eastman sandwich apparatus. Good separations of all test compounds fro
Autor:
K. Thomas Finley, Robert E. Gilman
Publikováno v:
Journal of Chromatography A. 22:36-40
Benzaldehyde 2.4-DNPH and 19 mono-sbustituted benzaldehyde 2,4-DNPH's have been chromatographed by thin-layer techniques. Conditions are reported for the separation of ten of the substituted compounds from binary mixtures with benzaldehyde 2,4-DNPH.
Autor:
Robert E. Gilman, Robert C. Elderfield
Publikováno v:
Phytochemistry. 11:339-343
Four indole alkaloids have been isolated and characterized from the tree bark of Alstonia muelleriana Domin. One of these is the previously known dimeric indole alkaloid, villalstonine (I). A second probably dimeric indole alkaloid, alstonisidine (II
Publikováno v:
Journal of the American Chemical Society. 94:2478-2482
Publikováno v:
Journal of Chromatography A. 44:569-572
The thin-layer chromatographic separation of alkyl and halogen substituted benzaldehyde 2,4-dinitrophenylhydrazones has been studied using a zinc carbonate adsorbant on glass plates and a 90% carbon disulfide-10% chloroform solvent mixture as the elu
Autor:
Robert E. Gilman, Léo Marion
Publikováno v:
Canadian Journal of Chemistry. 40:1713-1716
not available
Autor:
Robert E. Gilman, Léo Marion
Publikováno v:
Tetrahedron Letters. 3:923-925
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Die saurekatalysierte Umlagerung des optisch reinen (+)-(S)-Paracyclophans (I) in Dichlormethan bei 0°C liefert das optisch reine (+)-(S)-Metaparacyclophan (II) (52% Ausbeute; Mechanismus).