The stereo-and regioselective elaboration of a bromohydrin from an olefinic precursor and Pummerer ene reaction for carbon carbon bond formation are the key steps in a novel and flexible synthesis of xylo-phytosphingosine and threo-sphingosine.
β¦ LIBER β¦
Enantioselective total synthesis of (2S,3R,4R)-d-xylo-phytosphingosine from substituted azetidin-2-one
β Scribed by Ganesh Pandey; Dharmendra Kumar Tiwari
- Book ID
- 108285419
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 197 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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