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Selectivity chemo

This chapter will briefly survey some basic physical and chemical properties of water as well as the possible relevance of these properties to aqueous organic chemistry in terms of reactivity, selectivity (chemo-, regio-, and stereo-), and phase-separations. [Pg.22]

In organic synthesis, chemical transformation with a negative volume of activation (AVI) can be improved by application of high pressure, leading in many cases to an increase of the yield, an enhancement of the reaction rate, and an improvement of the selectivity (chemo-, regio- and stereoselectivity). This is especially true for cycloadditions with AVt values of approximately -50 cm3 mol"1 [1]. [Pg.566]

Since the first Symposium was held, research activities have rapidly expanded as has the support provided by industry. Thus 104 Abstracts were submitted (an increase of 44 on the first symposium), closely related to the symposium theme. Moreover, the scientific contribution made by industry was also greater than at the previous symposium since this time a third of the papers was presented by researchers solely from industry (5 papers) or in collaboration with researchers from Universities (16 papers). The transformations studied were this time much more complex, covering all aspects of selectivity chemo, regio and stereo-selectivity having been frequently considered. [Pg.622]

In attacking a synthetic target, the critical question about the suitability of any method involves selectivity chemo-, regio-, diastereo- and enantio-selectivity. Both from an educational point-of-view for the reader who wants to leam about a new field, and an experimental viewpoint for the practitioner who seeks a reference source for practical information, an organization of the chapters along the theme of selectivity becomes most informative. [Pg.1313]

Fig. 12 First enantio-selective, chemo-enzymatic synthesis of the monoterpenoid indole alkaloid (-)-akagerine, member of the family of Strychnos alkaloids... Fig. 12 First enantio-selective, chemo-enzymatic synthesis of the monoterpenoid indole alkaloid (-)-akagerine, member of the family of Strychnos alkaloids...
Messersmith, E. K., Leonardo, E. D., Shatz, C. J., Tessier-Lavigne, M., Goodman, C. S., and Kolodkin, A. L. (1995). Semaphorin III can function as a selective chemo-repellent to pattern sensory projections in the spinal cord. Neuron 14, 949-959. [Pg.104]

Because of the large variety of sulfur compounds, this chapter will be limited to thioacetals, sulfides, sulfoxides and sulfones. Many examples, selected from recent total syntheses of natural products, will emphasize the selectivity (chemo-, regio-, diastereo- and enantio-selectivity) of these reactions. [Pg.134]

More selective (types of selectivity chemo-selectivity, regio-selectivity, diastereo-selectivity, and enantio-selectivity)... [Pg.102]

Control of selectivity (chemo, regio, stereo, and enantioselectivity) is among the most important objective in organic synthesis. The efficient use of reaction conditions (temperature, time, solvent, etc.), kinetic or thermodynamic control, protecting or activating groups (for example chiral auxiliaries), and catalysts (including chiral catalysts) have all been used to obtain the desired isomer. [Pg.220]

Does the solvated species react more efficaciously and selectively (chemo, enantio, regioselectively)... [Pg.320]

Over the last few decades, transition-metal complexes have emerged as extremely useful synthetic tools for forming heterocycles. They often impart high selectivities (chemo, regio and stereo) seldom observed in classical synthetic methods. Moreover, the efficacy of these reactions, the possibility of employing mild conditions, and in many cases their use in catalytic quantities, all place metals as attractive precursors for orchestrating these transformations. ... [Pg.104]


See other pages where Selectivity chemo is mentioned: [Pg.25]    [Pg.81]    [Pg.263]    [Pg.764]    [Pg.67]    [Pg.508]    [Pg.807]    [Pg.114]    [Pg.508]    [Pg.81]    [Pg.7]    [Pg.1]    [Pg.157]    [Pg.377]    [Pg.1]    [Pg.337]    [Pg.764]    [Pg.186]    [Pg.77]    [Pg.1]   
See also in sourсe #XX -- [ Pg.15 , Pg.319 ]




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