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Natural products chemical synthesis

Chen, RE. Huang, J. (2005) Reserpine A Challenge for Total Synthesis of Natural Products. Chemical Reviews, 105, 4671-4706. [Pg.198]

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]

Lundt I (2003) Iminosugars, isoiminosugars, and carbasugars from activated carbohydrate lactones efficient synthesis of biologically important compounds. In Witzak ZJ, Tatsuta K (eds) Carbohydrate synthons in natural products chemistry synthesis, functionalization and applications. ACS Symposium Series, vol 841. American Chemical Society, Washington, DC,pp 117-140... [Pg.56]

Oikawa, Y, Nishi, T, Yonemitsu, O, Chiral synthesis of polyketide-derived natural product. Chemical correlation of chiral synthons, derived from D-glucose for the synthesis of erythromycin A, with chemical cleavage products of the natural antibiotic, J. Chem. Soc., Perkin. Trans. 1, 27-33, 1985. [Pg.572]

Witczak, Zbigniew J., Kuniaki Tatsuta, American Chemical Society Division of Carbohydrate Chemistry, and American Chemical Society. Carbohydrate Synthons in Natural Products Chemistry Synthesis, Functionalization, and Applications. ACS Symposium Series, no. 841. Washington, D.C. American Chemical Society, 2003. [Pg.308]

Within the following sections on general methodology, examples of oxindoles with relatively simple substitution patterns have been selected for making reasonable comparisons between different strategies for bond construction. Applications of methods toward the synthesis of densely functionalized oxindoles within sensitive chemical environments appear within the section on natural product total synthesis. [Pg.398]

The synthesis of carbocycles via a two-component cascade reaction in an asymmetric fashion has attracted much attention from the chemical community. Due to his importance in natural products, the synthesis of cyclopropanes, cyclopentanes, and cyclohexanes has been one of the common goals for organocatalytic methodologies. The high stereoselectivity achieved, green procedures, and soft conditions make this organocatalytic approximation one of the most attractive ones to build complex cyclic scaffolds. [Pg.357]

There are essentially three methods to prepare flavors (i) extraction from nature (ii) chemical synthesis and (iii) biotechnological production. [Pg.274]

Chen, D. Y. K., Pouwer, R. H., Richard, J.-A. (2012). Recent advances in the total synthesis of cyclopropane-containing natural products. Chemical Society Reviews, 41,... [Pg.146]

Natural product total synthesis has long served as a motivation for developing new chemical reactions. The converse, in which new reactions inspire efforts in natural product synthesis, is also widely observed. The work that is described in this chapter shows that these efforts can be symbiotic, and that this relationship can be useful for studying the biological activity of complex molecules. [Pg.188]

In summary, based on the above NMR evidence, I committed to structure 9 shown in Figure 6. It is at this point in the story that I draw the readers attention to the fact that it has become increasingly common that natural products that have their chemical structures elucidated by NMR spectroscopy have those structures later revised, usually as a result of a natural product total synthesis campaigns Sleepless night 1. [Pg.255]

FROM BIOSYNTHESIS TO TOTAL SYNTHESIS STRATEGIES TOWARD THE NATURAL PRODUCT CHEMICAL SPACE... [Pg.10]

Molecules with chirality centers are very common both as naturally occurring sub stances and as the products of chemical synthesis (Carbons that are part of a double bond or a triple bond can t be chirality centers)... [Pg.284]

Because there are four chirality centers and no possibility of meso forms there are 2" or 16 stereoisomeric hexoses All 16 are known having been isolated either as natural products or as the products of chemical synthesis... [Pg.306]


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See also in sourсe #XX -- [ Pg.194 , Pg.195 , Pg.196 ]




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