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Natural products significance

Tsuji Allylation A significant contribution to the field of asymmetric ketone alkylation is the Tsuji allylation. This method represents one of the only catalytic methods for asymmetric alkylation that has been suitably successful for application in the context of complex natural products. Significantly, this method also allows for the formation of all carbon quaternary stereocenters. [Pg.196]

The odor detection-threshold values of organic compounds, water, and mineral oil have been determined by different investigators (Table 2 and 3) and may vary by as much as 1000, depending on the test methods, because human senses are not invariable in their sensitivity. Human senses are subject to adaption, ie, reduced sensitivity after prolonged response to a stimulus, and habituation, ie, reduced attention to monotonous stimulation. The values give approximate magnitudes and are significant when the same techiriques for evaluation are used. Since 1952, the chemistry of odorous materials has been the subject of intense research (43). Many new compounds have been identified in natural products (37—40,42,44—50) and find use in flavors. [Pg.11]

The optical purities were determined solely from the optical rotations of the (/ -cyanohydrins thus obtained. Only for (/ )-a-hydroxybcnzeneacetonitrile, available from benzaldehyde, was an optical purity determined by comparison with the natural product. Variation of the reaction conditions (pH, temperature, concentration) in water/ethanol led to no appreciable improvementsl4. The use of organic solvents that are not miscible with water, but in which the enzyme-catalyzed reaction can still take place, resulted in suppression of the spontaneous addition to a significant extent, whereas the enzyme-catalyzed formation of cyanohydrins was only slightly slower (Figure l)13. [Pg.668]

An area in which catalytic olefin metathesis could have a significant impact on future natural product-directed work would be the desymmetrization of achiral molecules through asymmetric RCM (ARCM) or asymmetric ROM... [Pg.359]

This series in heterocychc chemistry is being introduced to collectively make available critically and comprehensively reviewed hterature scattered in various journals as papers and review articles. All sorts of heterocyclic compounds originating from synthesis, natural products, marine products, insects, etc. will be covered. Several heterocyclic compounds play a significant role in maintaining life. Blood constituents hemoglobin and purines, as well as pyrimidines, are constituents of nucleic acid (DNA and RNA). Several amino acids, carbohydrates, vitamins, alkaloids, antibiotics, etc. are also heterocyclic compounds that are essential for life. Heterocyclic compounds are widely used in clinical practice as drugs, but all applications of heterocyclic medicines can not be discussed in detail. In addition to such applications, heterocyclic compounds also find several applications in the plastics industry, in photography as sensitizers and developers, and the in dye industry as dyes, etc. [Pg.9]

Interestingly, significant progress has been made for the hydroamination of more reactive substrates such as styrenes, alkynes, dienes, and allenes. Specifically, highly selective catalysts have been discovered for the synthesis of fine chemicals (pharmaceuticals, natural products, chemical intermediates). In this area however, the problem of catalyst stabiUty can also be questioned in several cases. [Pg.132]


See other pages where Natural products significance is mentioned: [Pg.463]    [Pg.649]    [Pg.280]    [Pg.463]    [Pg.649]    [Pg.280]    [Pg.27]    [Pg.29]    [Pg.5]    [Pg.32]    [Pg.33]    [Pg.120]    [Pg.111]    [Pg.61]    [Pg.62]    [Pg.68]    [Pg.71]    [Pg.509]    [Pg.309]    [Pg.209]    [Pg.68]    [Pg.365]    [Pg.262]    [Pg.407]    [Pg.506]    [Pg.562]    [Pg.677]    [Pg.732]    [Pg.735]    [Pg.750]    [Pg.278]    [Pg.512]    [Pg.594]    [Pg.724]    [Pg.240]    [Pg.205]    [Pg.208]    [Pg.119]    [Pg.286]    [Pg.155]    [Pg.440]    [Pg.235]    [Pg.239]    [Pg.724]    [Pg.111]    [Pg.201]    [Pg.61]    [Pg.1231]   
See also in sourсe #XX -- [ Pg.9 , Pg.10 , Pg.11 , Pg.12 ]




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