Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Herbert Bosshardt"'
Publikováno v:
Journal of Pharmaceutical Sciences. 83:131-136
The dissolution rate profile of a new modified-release (MR) oral tablet of ketotifen (Zaditen SRO tablet, Sandoz Ltd.) was determined under different conditions (pH, rpm, paddle or basket) with the U.S.P. apparatus. Three different variants of MR tab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e165a5c3f478b7c216843645ea784a53
https://doi.org/10.1002/jps.2600830205
https://doi.org/10.1002/jps.2600830205
Autor:
Herbert Bosshardt, Manfred Hesse
Publikováno v:
Angewandte Chemie International Edition in English. 13:252-266
The mass spectral decomposition of di- and polyfunctional alkanes is characterized essentially by two, fundamentally different reactions: On the one hand the structures of the fragment ions are determined by separated degradation of each functional g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88eed66f6bdde4270f092cb42289a826
https://doi.org/10.1002/anie.197402521
https://doi.org/10.1002/anie.197402521
Publikováno v:
Helvetica Chimica Acta. 62:2712-2723
Contribution to the Absolute Configuration of the Spermine Alkaloids O-Methylorantine and Aphelandrine The absolute configuration of the spermine alkaloid O-methylorantine (1) isolated from Chaenorhinum minus (L.) WILLK. ET LGE. and Ch. villosum (L.)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f72be4cc262909eade464bd9ec13e95
https://doi.org/10.1002/hlca.19790620823
https://doi.org/10.1002/hlca.19790620823
Autor:
Manfred Hesse, Herbert Bosshardt
Publikováno v:
Angewandte Chemie. 86:256-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2edd37a4bca3ba3a10d34b806c5abf63
https://doi.org/10.1002/ange.19740860704
https://doi.org/10.1002/ange.19740860704
Publikováno v:
Helvetica Chimica Acta. 61:2646-2671
The structure of the spermine alkaloid aphelandrine from Aphelandra squarrosa NEES The new spermine alkaloid aphelandrine (2) has been isolated from Aphelandra squarrosa NEES. By oxidation of 2 with KMnO4 followed by methylation (CH2N2) 12 and 14 cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5f96e184f73f38e90e3a781740e393e
https://doi.org/10.1002/hlca.19780610735
https://doi.org/10.1002/hlca.19780610735
Autor:
Rattan S. Sood, Fathy S. Matough, James P. Kutney, Brian R. Worth, Vicente E. Ridaura-Sanz, Ying Hung So, John F. Beck, Rodney A. Badger, Herbert Bosshardt
Publikováno v:
Canadian Journal of Chemistry. 57:289-299
A synthesis of 16,17-dihydrosecodin-17-ol and of secodine is described. Various indole derivatives were elaborated to a series of pyridinium salts, potential precursors for 1,2- and 1,6-dihydropyridine compounds exemplifying the proposed biointermedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::462a964b18b6bf376a3082dbceaf023d
https://doi.org/10.1139/v79-048
https://doi.org/10.1139/v79-048
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d569a9e96ed2629def9258b9809c41b
https://doi.org/10.1002/chin.197905303
https://doi.org/10.1002/chin.197905303
Autor:
Manfred Hesse, Herbert Bosshardt
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fdd8b1eeea7c649b00edeb6648e10f8
https://doi.org/10.1002/chin.197423072
https://doi.org/10.1002/chin.197423072
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9125641d8aca85f4e0208d1907ce834d
https://doi.org/10.1002/chin.198014349
https://doi.org/10.1002/chin.198014349
A Facile Route to a Sensitive Terpene Alcohol—Regio-unselective Metalation ofα-Terpinene as Key Step
Publikováno v:
Angewandte Chemie International Edition in English. 19:303-303
Treatment of a-terpinene (I, R = H) with BuLi-KOCMe3 followed by FB(OMe)2 and then alk. H2O2 soln. gave 44% anthemol (I, R = OH). The metalation step of a-terpinene presumably gave 3 pentadiene-K species (II-IV), which reacted with D2O and ClSiMe3 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d86884888f9510d4084a73261145d39f
https://doi.org/10.1002/anie.198003031
https://doi.org/10.1002/anie.198003031