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Avermectins synthetic approaches

Of the numerous synthetic approaches to the southern half of the avermectins published to date only one (by Danishefsky et al.) has led to a successful total synthesis of a naturally occurring avermectin. The feasibility of this approach, which utilizes a Michael-Aldol sequence to establish the ring system, was first demonstrated by Armistead and Danishefsky [109] in the synthesis of model system 19. In their synthesis, chiral aldehyde 14, which is readily available... [Pg.82]

The preparation of avermectins has been carried out by fermentation, microsomal oxidation of early fermentation compounds and by semi-synthetic methods [57,113]. Approaches to synthesize some avermectins such as abamectin [114] and ivermectin [115-117] have also been published. Recently the total synthesis of aver-mectin [118], avermectin A g [119] and the aglycones of avermectin A g and B g [120,121] have been reported. [Pg.89]


See other pages where Avermectins synthetic approaches is mentioned: [Pg.145]    [Pg.68]    [Pg.74]    [Pg.416]    [Pg.420]    [Pg.554]    [Pg.540]    [Pg.83]    [Pg.97]    [Pg.817]    [Pg.3575]    [Pg.67]   


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