Abstract
The C-glycosidic analogue of α-L-rhamnose 1-phosphate has been stereoselectively synthesised reacting 2,3,4-tri-O-benzyl-L-rhamnopyranose with tetraethyl methylenediphosphonate and sodium hydride in diglyme, and then deprotecting with iodotrimethylsilane.
Original language | English |
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Pages (from-to) | 5567-5568 |
Number of pages | 2 |
Journal | Tetrahedron Letters |
Volume | 38 |
Issue number | 31 |
DOIs | |
Publication status | Published - 4 Aug 1997 |
Externally published | Yes |