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Possible biosynthetic pathways for streptovaricins

Possible biosynthetic pathways from a 2,6-disubstituted piperidine to various dendrobatid alkaloids. The absolute configuration suggested for the precursor of gephyrotoxin 223AB is arbitrary. The absolute configuration of gephyrotoxin is based on x-ray

Possible biosynthetic pathways from L-lysine to pipecolic acid

Possible biosynthetic pathways leading to asparagusic acid .

Possible biosynthetic pathways leading to ipsdienol .

Possible biosynthetic pathways leading to sulcatone .

Possible biosynthetic pathways of aconitine-type Ci9-diterpenoid alkaloids

Possible biosynthetic pathways of gentianine

Possible biosynthetic pathways of noncondensed aromatic lichen polyketides from a -polyoxomethylene chain. The starting positions are indicated by heavy lines, while the dotted lines indicate the theoretically still possible formation of such compounds from two separate units.

Possible biosynthetic pathways of vasicine .

Possible biosynthetic pathways to Fe24

Possible biosynthetic pathways to mammalian -reticuline.

Possible biosynthetic pathways to pipecolic acid .

Possible biosynthetic relationship between Lachnanthe,

Possible biosynthetic relationship between naphthyl isoquinoline alkaloids and cooccurring naphthoquinones.

Possible biosynthetic route to mulinane, azorellane, yaretane, and madreporane carbon skeletons of diteipenes isolated from high elevation Azorella cushion plants, according to Loyola et al., 2002. Note the unusual demethylation step in the azorellane - yaretane conversion.

Possible biosynthetic route to mulinane, azorellane, yaretane, and madreporane carbon skeletons of diterpenes isolated from high elevation Azorella cushion plants, according to Loyola et ah, 2002. Note the unusual demethylation step in the azorellane - yaretane conversion.

Possible biosynthetic route to skyrin and rugulosin

Possible biosynthetic route to the Cephalotaxus alkaloids.

Possible biosynthetic route towards coumarin. dimethylallyl transferase and or UV light. The enzymes have not yet been identified.

Possible biosynthetic routes leading from dopa to the betalain pigments of toadstools.

Possible biosynthetic routes leading from the shikimic acid pathway to betalains and the coexisting flavonoids in betalain-bearing members of the Caryophyl-lales.

Possible biosynthetic sequence for O-linked oligosaccharides. The sequential addition of monosaccharide units for the O-linked oligosaccharide synthesis is exemplified for some core structures with an initial N-acetylglucosamine residue. Glycosylation may continue with stepwise addition of Gal, GlcNAc, Fuc and Sia. The linear codes are used

Possible biotransfonnation of orellanine to orelline.

Possible biotransformation pathway from bisbenzyltetrahydroisoquinolines



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