Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bowman, Phil B."'
Autor:
Thomas J. Thamann, Jane E. Guido, Bowman Phil B, Kathleen A. Farley, Frank W. Crow, Brenda S. Vonderwell, Russell H. Robins, Gary E. Martin, Richard F. Smith, Wayne K. Duholke, Sandra M. Sims, Jay C. Brumfield
Publikováno v:
Magnetic Resonance in Chemistry. 36:S11-S16
A method is described for unequivocally establishing the site of N-oxidation which relies on the relatively large downfield shift of aliphatic nitrogen resonances following oxidation. The technique described is based on 15N at natural abundance and d
Autor:
Martin, Gary E., Robins, Russell H., Bowman, Phil B., Duholke, Wayne K., Farley, Kathleen A., Kaluzny, Brian D., Guido, Jane E., Sims, Sandra M., Thamann, Thomas J., Thompson, Brian E., Nishimura, Toshihide, Noro, Yukimi, Tahara, Tsutoma
Publikováno v:
Journal of Heterocyclic Chemistry; Jan1999, Vol. 36 Issue 1, p265-270, 6p
Publikováno v:
Journal of Chromatography A. 283:281-287
An absorption high-performance liquid chromatography assay for the quantitative determination of prostaglandins A1 and B1 in alprostadil (prostaglandin E1) and in Prostin VR Pediatric Sterile Solution was developed. Prostaglandins A1 and B1 have been
Autor:
Peter W Dame, Bowman Phil B
Publikováno v:
Journal of AOAC INTERNATIONAL. 57:1128-1131
A procedure is described for the determination of trichlorfon in a soluble powder formulation by gas-liquid chromatography. Silylation prevents on-column degradation of trichlorfon to dichlorvos. The procedure provides quantitative recovery from the
Autor:
Bowman Phil B, Patrick A. Hartman
Publikováno v:
Journal of Chromatography A. 291:283-290
Two complementary high-performance liquid chromatographic assays for the quantitation of epoprostenol sodium (PGI 2 ) and seven potential impurities in epoprostenol sodium bulk drug are described. A reversed-phase assay using a mobile phase of aceton
Publikováno v:
Journal of Chromatography A. 283:273-280
An adsorption high-performance liquid chromatographic method suitable for the quantitative determination of the purity of alprostadil (prostaglandin E1) bulk drug and of the concentration of alprostadil in Prostin V.R. Pediatric® Sterile Solution is
Autor:
Martin, Gary E., Robins, Russell H., Bowman, Phil B., Duholke, Wayne K., Farley, Kathleen A., Kaluzny, Brian D., Guido, Jane E., Sims, Sandra M., Thamann, Thomas J., Thompson, Brian E., Nishimura, Toshihide, Noro, Yukimi, Tahara, Tsutoma
Publikováno v:
Journal of Heterocyclic Chemistry; January 1999, Vol. 36 Issue: 1 p265-270, 6p
Autor:
Farley, Kathleen A., Bowman, Phil B., Brumfield, Jay C., Crow, Frank W., Duholke, Wayne K., Guido, Jane E., Robins, Russell H., Sims, Sandra M., Smith, Richard F., Thamann, Thomas J., Vonderwell, Brenda S., Martin, Gary E.
Publikováno v:
Magnetic Resonance in Chemistry; June 1998, Vol. 36 Issue: Supplement 1 pS11-S16, 6p
Autor:
Bowman Phil B, Leo W. Brown
Publikováno v:
Journal of chromatographic science. 12(6)
Publikováno v:
Journal of chromatography. 408
An isocratic high-performance liquid chromatographic (HPLC) method was developed to determine the enantiomeric purity of a benzindene prostaglandin (U-62,840) which is currently being evaluated for pharmaceutical applications. The enantiomers were co