𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Dephosphonylation of protected deoxynucleoside and oligodeoxynucleotide H-phosphonates

✍ Scribed by Colin B. Reese; Cristina Visintin

Book ID
104261968
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
211 KB
Volume
40
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

The conversion of four 5'-O-(4,4'-dimethoxytrityl)-2'-deoxyribonucleoside 3'-H-phosphonates 1 (B---4, 5, 6 and 7) into their partially-protected nucleoside precursors 3 (B--4, 5, 6 and 7, respectively) in good isolated yields is described. The procedure used is also suitable for the dephosphonylation of protected oligonucleotide H-phosphonate blocks.

πŸ“œ SIMILAR VOLUMES

Chemistry and Application of H-Phosphona
Chemistry and Application of H-Phosphonates || Reactivity of H-Phosphonates
✍ Troev, Kolio D. (author) πŸ“‚ Article πŸ“… 2006 πŸ› Elsevier 🌐 English βš– 797 KB

**Chemistry and Application of H-Phosphonates** is an excellent source for those planning the synthesis of new phosphorus-containing compounds and in particular derivatives containing a phosphonate, phosphoramide or phosphonic acid diester group. The rich chemistry, low cost and easy availability of

Chemistry and Application of H-Phosphona
Chemistry and Application of H-Phosphonates || Reactivity of H-Phosphonates
✍ Troev, Kolio D. (author) πŸ“‚ Article πŸ“… 2006 πŸ› Elsevier 🌐 English βš– 797 KB

**Chemistry and Application of H-Phosphonates** is an excellent source for those planning the synthesis of new phosphorus-containing compounds and in particular derivatives containing a phosphonate, phosphoramide or phosphonic acid diester group. The rich chemistry, low cost and easy availability of