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- W2950714251 abstract "Publisher Summary This chapter discusses the mechanism of oxidative coupling, which is an important reaction in the biosynthesis of secondary plant metabolites; it has been estimated that the biosynthesis of more than 10% of alkaloids involves one or more oxidative coupling steps. A more or less complete list of such compounds compiled from the Dictionary of Natural Products is given as an appendix in the chapter. Curare alkaloids are the dimers of l-benzyl-1,2,3,4-tetrahydroisoquinolines linked by one, two, or even three ether bridges positioned in a most varied manner. Both diary1 and diarylether type compounds occur in aromatic carboxylic acids. Monocyclic phenols readily form dimmers and oligomers involving both C–C and diaryl ether bonds. Oxidative dimerization of two molecules of gallic acid give rise to ellagic acid, which is, in the dicarboxylic acid form, the basic building block of a very large number of highly complex natural products containing at least one, but usually two or more, molecules of ellagic acid linked to glucose or some of its transformation products." @default.
- W2950714251 created "2019-06-27" @default.
- W2950714251 creator A5022888378 @default.
- W2950714251 creator A5065240177 @default.
- W2950714251 date "1997-01-01" @default.
- W2950714251 modified "2023-10-18" @default.
- W2950714251 title "Natural products by oxidative phenolic coupling phytochemistry, biosynthesis and synthesis" @default.
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