Abstract
The reaction of 2,3-isopropylidene-5-trityl-d-ribofuranose with methylenetriphenyl-phosphorane and the subsequent mercuriocyclization, iodomercuriation and Arbuzov reaction, allow a highly stereoselective entry to the phosphono analog of α-d-ribose 1-phosphate.
| Original language | English |
|---|---|
| Pages (from-to) | 5937-5938 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 25 |
| Issue number | 51 |
| DOIs | |
| Publication status | Published - 1984 |
| Externally published | Yes |
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Dive into the research topics of 'High stereoselective synthesis of diethyl (2,3-isopropylidene-5-trityl-α-d-ribofuranosyl)-methanephosphonate, a precursor to the phosphono analog of α-d-ribose 1-phosphate'. Together they form a unique fingerprint.Cite this
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