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Natural products system

Yolk colour plays a role in consumer acceptance, but the preferred colour varies in different countries. Yolk colour has no relation to nutrient content, flavour or freshness, but is often enhanced in conventional production systems by addition of synthetic pigments to the animal feed. In organic production, synthetic yolk pigments are prohibited and this normally results in paler yolks, but may also lead to greater variability in yolk colour intensity. In many European countries paler yolk colour is perceived by consumers as being associated with less natural production systems, an issue that clearly needs to be addressed by improved consumer information. [Pg.123]

Diels-Alder reaction is an extremely useful synthetic tool the reaction displays excellent regio- and stereoselectivity, and these properties have been exploited in the synthesis of many natural product systems.52... [Pg.137]

Several other natural products systems have been studied, some quite extensively, by NMR methodology, however space constraints prohibt detailed discussion of these systems therefore only important leading references will be given. Extensive NMR studies on amino acids and small peptides have been performed by Lauterwein and coworkers [116-119], by Fiat and coworkers [120-123] and others [124]. Several studies have used l O-enriched dioxygen and carbon monoxide to study by NMR techniques the interactions of these biochemically important small molecules with various proteins [125-128]. A number of investigators have explored the properties and interactions of nucleic acid bases [129,130], nucleosides [131,132], nucleotides [133-138] and one report has appeared in which NMR spectroscopy approaches were applied to the study of small molecule-DNA interactions [139]. A recent report describes the careful analysis of the effect of structure on NMR chemical shifts of over forty hydroxyterpenoids [140]. A study of the 1 0 NMR spectroscopy of over thirty steroid ketones, acids, esters and alcohols enriched with has recently appeared [141]. [Pg.593]

If functionality is a requirement, polyhydroxy compounds are common in nature (86). Carbazole and amide types have also been recognized in natural product systems (86) as has nitrogen in many alkaloid systems (84). [Pg.389]

In the case of the classical synthesis of phenolic compounds it is remarkable that in one text on natural products (ref. 2) one quarter of the compounds discussed are concerned with phenols or their methyl ethers. In another general account of organic synthesis (ref. 3) concerned with a vast array of structural types, phenolic systems comprise between 10 and 15% while in a more recent account of synthesis (ref. 4) again of natural products of all types, more than 115 compounds from 613 listed have phenolic or phenolic ether structures. This is a consequence of the prevalence of polyketide biosynthesis in natural product systems (ref. 5). [Pg.558]

Keywords Amaryllidaceae alkaloid plant secondary metabolism alkaloid biosynthesis natural products systems biology galanthamine... [Pg.53]

FIGURE 10.23 Routes to coal from natural product systems. (From Volborth, A., Analytical Methods for Coal and Coal Products, Academic Press, Inc., New York, Vol. Ill, Chapter 55, 1979.)... [Pg.320]

The photoelectrocyclization of stilbene derivatives under oxidative conditions (air or iodine generally used as oxidants) has been largely exploited for the synthesis of various natural product systems. As an example, the benzophenan-thridine ring of kibdelone 15 was best prepared from the stilbene derivative 14 by irradiation in the presence of 1.1 equivalent iodine and excess THF as a trap for the cogenerated HI that would otherwise cause extensive degradation of the products (Scheme 8.4) [4]. [Pg.207]


See other pages where Natural products system is mentioned: [Pg.487]    [Pg.570]    [Pg.473]    [Pg.565]    [Pg.473]    [Pg.565]    [Pg.109]    [Pg.302]    [Pg.310]    [Pg.473]    [Pg.565]    [Pg.567]    [Pg.572]    [Pg.194]    [Pg.277]    [Pg.194]    [Pg.164]    [Pg.564]    [Pg.553]    [Pg.630]   
See also in sourсe #XX -- [ Pg.331 ]




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