The pseudo tetrasaccharide 2 was designed to mimic diol 3 was enantioselectively synthesized by an asymmetric Diels-Alder reaction, followed by dihydroxylation of the ganglioside GM1, the membrane receptor of both the cholera toxin and of the heat-labile toxin of E. coli. Compound 2 resulting cycloh
โฆ LIBER โฆ
Synthesis of Ceramide Mimics with a Pseudo Cyclic Framework.
โ Scribed by Hikokazu Suzuki; Michiko Mori; Motonari Shibakami
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 54 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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