The C-glycosidic analogue of ct-L-rhamnose l-phosphate has been stereoselectively synthesised reacting 2,3,4-tri-O-benzyl-L-rhamnopyranose with tetraethyl methylenediphosphonate and sodium hydride in diglyme, and then deproteeting with iodotrimethylsilane.
A theoretical study of the conformational behavior of analogues of α-l-rhamnose-1-phosphate
✍ Scribed by Federica Compostella; Franca Marinone Albini; Fiamma Ronchetti; Lucio Toma
- Book ID
- 108080129
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 426 KB
- Volume
- 339
- Category
- Article
- ISSN
- 0008-6215
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