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Aflavinine

The formation of aflavazole (381) from the proposed common biosynthetic intermediate, nominine (448), could proceed through aflavinine (451) and 20,26-dihydrooxyaflavinine (452) by way of the transformations depicted in... [Pg.177]

Scheme 3.18. The occurrence of nominine (448), aflavinine (451), 20,25-dihydro-oxyaflavinine (452), and aflavazole (381) in the sclerotia of the same Aspergillus spp. may be considered circumstantial evidence in favor of this biogenetic proposal (347). Scheme 3.18. The occurrence of nominine (448), aflavinine (451), 20,25-dihydro-oxyaflavinine (452), and aflavazole (381) in the sclerotia of the same Aspergillus spp. may be considered circumstantial evidence in favor of this biogenetic proposal (347).
See other pages where Aflavinine is mentioned: [Pg.178]    [Pg.146]    [Pg.18]    [Pg.228]    [Pg.228]    [Pg.229]    [Pg.247]    [Pg.440]    [Pg.178]    [Pg.146]    [Pg.18]    [Pg.228]    [Pg.228]    [Pg.229]    [Pg.247]    [Pg.440]   
See also in sourсe #XX -- [ Pg.228 ]

See also in sourсe #XX -- [ Pg.247 , Pg.249 ]



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Aflavinine, 3-demethylsynthesis Ajmalicine

Aflavinine, 3-demethylsynthesis Knoevenagel reaction

Aflavinine, 3-demethylsynthesis Mannich reaction

Aflavinine, 3-demethylsynthesis synthesis

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