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Chemical Syntheses of Biosynthetic Intermediates

Works concerning the chemical synthesis of intermediates along the ajma-line (1) biosynthesis pathway, as significant as parts of alkaloid biosynthesis research, were also mentioned here. [Pg.7]

Elegant chemical synthesis of geissoschizine (46) and geissoschizine-type derivatives which are important for early steps in Rauvolfia alkaloid biosynthesis, have been reported decades ago by Winterfeldt and coworkers. [Pg.8]

First enantiospecific total syntheses of biogenetic intermediates on the way to sarpagine (5), such as polyneuridine aldehyde (46) or 16-epi-vellosimine (49), have been reported recently by Cook and coworkers. For most recent publications see Refs 43,44. [Pg.9]

A very interesting enantioselectively synthetic approach to sarpagine alkaloids, developed very recently by Gaich and coworkers needs to be mentioned here. For a review in this field see Ref 46. [Pg.9]


See other pages where Chemical Syntheses of Biosynthetic Intermediates is mentioned: [Pg.7]   


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