AbstracL A versatile, efficient route to ribosylhopane with control over all asymmetric carbon atoms of the side-chain is presented. The synthesis is based on two chain elongations starting from diploptene by subsequent additions of two acetylenic moieties. In a key step a keto-propiolate is stereos
β¦ LIBER β¦
ChemInform Abstract: Synthesis of Ribosylhopane (I), the Putative Biosynthetic Precursor of Bacterial Triterpenoids of the Hopane Series.
β Scribed by Tore Duvold; Michel Rohmer
- Book ID
- 101888860
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 25 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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