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Isolation general strategy

Zraro-pyridine donors) have been determined,and the fac and mer isomers of [Ru(219)3] + and two diastereomers of [Ru(219)2(bpy)] " " have been isolated using HPLC, and EPR spectroscopic data for the singly reduced species have been analyzed. A general strategy for the synthesis of [Ru(218)3]"+ has been included in a study of routes to tris(bpy), tris(phen), and tris(218) complexes of Ru and A comparison has been made between the photoinduced oxidative... [Pg.625]

The results obtained by Warwel and Winkelmiiller provided the groundwork for the development of product-selective CM. In these reactions, the observed product selectivity was attributed to the diminished CM reactivity of stilbene relative to styrene. Indeed, subjecting an isolated homodimer to CM conditions constitutes a general strategy... [Pg.186]

F. Breviario, C. Garlanda, S. Ramponi, A. Mantovani, and A. Vecchi, A general strategy for isolation of endothelial cells from murine tissues. Characterization of two endothelial cell lines from the murine lung and subcutaneous sponge implants, Arterioscler. Thromb. Vase. Biol. 77 1599-1604 (1997). [Pg.242]

Fig. 7.3-3 General strategy for activity-based protein profiling (ABPP). Proteomes are treated with chemical probes that label active enzymes of a particular class (or classes) in a manner that allows for their detection, isolation, and identification. Active enzymes are denoted by open/unshaded active sites, with their inactive counterparts (e.g., zymogen or inhibitor-bound forms) shaded in black. Fig. 7.3-3 General strategy for activity-based protein profiling (ABPP). Proteomes are treated with chemical probes that label active enzymes of a particular class (or classes) in a manner that allows for their detection, isolation, and identification. Active enzymes are denoted by open/unshaded active sites, with their inactive counterparts (e.g., zymogen or inhibitor-bound forms) shaded in black.
Theonelladins A-D A novel alkylpyridines (15-18) were isolated from Theonella swinhoei and exhibit mild activities in vitro against murine lymphomas and epidermoid carcinoma [29]. Two stereoselective total syntheses of theonelladins A-D have been published to date. A general strategy was used involving the construction of a common carbon skeleton 15a (see Scheme 4). Although the successful completion of the synthesis of 15-18 was achieved, the final introduction of the amino group into the molecule was not a clean step. [Pg.590]

Here, we will discuss the general strategies followed in the isolation, identification, and structure elucidation of alkaloids. The various methods will be briefly discussed separately, with special reference to the applications for alkaloid analysis. We will not try to give a complete review of all work done on the structure elucidation of alkaloids. For reviews on the different classes of alkaloids we refer to the series The Alkaloids, Volumes 1-5 edited by Manske and Holmes (1950-1955), Volumes 6-16 by Manske (1955-1977), Volumes 17-20 by Manske and Rodrigo (1979-1981) and later volumes by Brossi (1983-1992), and Alkaloids Chemical and Biological Perspectives edited by Pelletier (since 1983). Furthermore, numerous review articles on different groups of alkaloids have been published particularly on isoquinoline alkaloids a series of reviews has appeared in the Journal of... [Pg.1]


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