## Abstract Ketide side chains (C~4~) were attached to the naphthoquinone 3 by reaction with the dienes 4 or 14 followed by BakerβVenkataraman rearrangement of esters 8 and 17 to attach the second protected Ξ²βdiketo side chain. Linear anellations of the corresponding naphthoquinone precursors 9 and
β¦ LIBER β¦
Synthesis of 4-Deoxyaklanonic acid and Its Microbial Conversion into Anthracyclinones
β Scribed by Prof. Dr. Karsten Krohn; Dr. Ernst Roemer; Michael Top; Dr. Christina Wagner
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 264 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0044-8249
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