Zobrazeno 1 - 10
of 42
pro vyhledávání: '"K Kasdorf"'
Autor:
MJ Alfa, GKM Harding, AR Ronald, RB Light, N MacFarlane, N Olson, P DeGagne, K Kasdorf, A Simor, KS MacDonald, L Louie
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 10, Iss 4, Pp 287-294 (1999)
OBJECTIVE: To monitor prospectively patients with Clostridium difficile-associated diarrhea (CAD) in a six hundred bed tertiary care hospital to determine which factors influenced the recurrence of the diarrhea.
Externí odkaz:
https://doaj.org/article/f3c21cdc5d5d4a84836e1a8c75348c32
Autor:
K Kasdorf, R. B. Light, L Louie, P. Degagne, G.K.M. Harding, Michelle J. Alfa, Kelly S. MacDonald, N. Olson, A. Simor, N MacFarlane, Allan R. Ronald
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 10, Iss 4, Pp 287-294 (1999)
OBJECTIVE: To monitor prospectively patients withClostridium difficile-associated diarrhea (CAD) in a six hundred bed tertiary care hospital to determine which factors influenced the recurrence of the diarrhea.DESIGN: A prospective, nonrandomized stu
Publikováno v:
Pure and Applied Chemistry. 69:383-388
FR-900848 is a pentacyclopropane nucleoside antifungal agent isolated from the fermentation broth of Streptoverricillium fervens. The full structure with relative and absolute stereochemistry of this unusual natural product were established by a comb
Autor:
W. W. Doubleday, David J. Williams, Anthony G. M. Barrett, Andrew J. P. White, G. J. Tustin, K. Kasdorf, Dieter Hamprecht
Publikováno v:
Chemical Communications. :1693-1700
The full structural elucidation of FR-900848, an antifungal pentacyclopropane nucleoside natural product from Streptoverticillum fervens, is reported. A series of model compounds are prepared using multiple asymmetric Simmons–Smith cyclopropanation
Autor:
K. Kasdorf, Anthony G. M. Barrett
Publikováno v:
Journal of the American Chemical Society. 118:11030-11037
Quatercyclopropane 31 was oxidized, homologated, reduced, and monocyclopropanated to provide the pentacyclopropane alcohol 35. Subsequent deoxygenation of alcohol 35 was effected using N-(phenylthio)succinimide (24) and tributylphosphine followed by
Publikováno v:
Journal of Heterocyclic Chemistry. 33:1545-1550
Publikováno v:
The Journal of Organic Chemistry. 61:3280-3288
Full structural elucidation of FR-900848, an antifungal pentacyclopropane nucleoside natural product from Streptoverticillium fervens, is reported. A series of model compounds were prepared using multiple asymmetric Simmons−Smith cyclopropanation r
Publikováno v:
ChemInform. 25
Double asymmetric Simmons–Smith cyclopropanation and Whitham elimination were used to prepare (E)-1,2-bis-[(1S,2S)-2-methylcyclopropyl]ethane, the dicyclopropylethene unit of FR-900848.
Autor:
W. W. Doubleday, David J. Williams, G. J. Tustin, Andrew J. P. White, K. Kasdorf, Anthony G. M. Barrett
Publikováno v:
ChemInform. 26
Two sequential asymmetric bicyclopropanation reactions were used to prepare (1R,3S,4R,6S,7S,9R,10S,12R)-quatercyclopropyl-1,12-dimethanol and (1S,3R,4R,6S,7S,9R,10R,12S)-quatercyclopropyl-1,12-dimethanol.
Publikováno v:
ChemInform. 26
Whitham elimination is used to prepare (Z)-1,2-bis[(1S,2S)-2-methylcyclopropyl]ethene, which along with the corresponding E-alkene, is used as a structural model to determine that the geometry of the dicyclopropylethene unit of FR-900848 is trans.