Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rupp Michael J"'
Publikováno v:
東海大学紀要農学部. 38:39-48
Autor:
Rupp, Michael J.
Publikováno v:
熊本大学社会文化研究. 15:271-304
Using data gathered from 1125 Japanese high school students, this study reports on an exploratory factor analysis (EFA) conducted on the Kambara Locus of Control Scale (K-LoC), a widely use instrument for measuring locus of control (LoC) in the Japan
Publikováno v:
Organic Letters. 2:2951-2954
A novel class of 2-fluoro-6-O-propargyl-11,12-carbamate ketolide derivatives of erythromycin has been synthesized for antibacterial SAR studies. Replacement of the C2-hydrogen by a fluorine atom allows the synthesis of 6-O-propargylic ketones and ele
Publikováno v:
Organic letters. 4(6)
[structure: see text] Bifunctional macrolides projecting an anchor group to the right or left spatial position of the lactone ring were synthesized. The regioselectivity of the key [3 + 2] cycloaddition process was controlled by the remote cladinose
Autor:
Patty Ewing, Angela M. Nilius, Leping Li, Ping Zhong, Zhenkun Ma, Peter A. Nemoto, Richard F. Clark, Rupp Michael J, Zhensheng Cao, Daniel T. W. Chu, Michael J. Mitten, Jeff Alder, Robert K. Flamm, Ly Tam Phan, Hong Yong, George Griesgraber, Antony A Brazzale, Sanyi Wang, Jacob J. Plattner, Virginia D. Shortridge, Yat Sun Or, J. Meulbroek, Suoming Zhang, Xiaolin Zhang
Publikováno v:
Journal of medicinal chemistry. 44(24)
A novel series of erythromycin derivatives has been discovered with potent activity against key respiratory pathogens, including those resistant to erythromycin. These compounds are characterized by having an aryl group tethered to the C-6 position o
Publikováno v:
ChemInform. 32
A novel class of 2-fluoro-6-O-propargyl-11,12-carbamate ketolide derivatives of erythromycin has been synthesized for antibacterial SAR studies. Replacement of the C2-hydrogen by a fluorine atom allows the synthesis of 6-O-propargylic ketones and ele
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