A convenient method for the synthesis of deoxyribonucleoside 3′-hydrogenphosphonates
✍ Scribed by Mitsuo Sekine; Sin-ichiro Narui; Tsujiaki Hata
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 262 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Evidence will be presented to show that the monofunctional phosphitylating reagents bis(N,N-di-ethylamino)chlorophosphine and salicylchlorophosphine are very effective for the preparation of 5'-O,N-protected d-nucleoside-3'-hydrogenphosphonates.
A simprijidprocedure for the synthesis ~f3,4~r~~-~-[nis(I-methylethyl)sityll-IH-pyrrole (21 is described together with its sequential halogen-metal exchange che&tty to @kd3,4-disubstitutedpwole.f. During efforts relating to the synthesis of analogues of the protein kinase C (PKC) activator,' lyngby