The stereoselective synthesis of cyclopropylphosphonate analogs of nucleotides
β Scribed by Jung Hwan Hah; Jun Mo Gil; Dong Young Oh
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 325 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
1-Alkenylphosphonic acid derivatives of purines have been proven to exhibit significant antiviral activity among these series of compounds. Here we disclose the stereoselective synthesis of the constrained analogs of 1-alkenylphosphonate derivatives of purines via intramolecular epoxide opening reaction of \d,6epoxyalkanephosphonates with subsequent Mitsunobu coupling reactions with purine bases.
π SIMILAR VOLUMES
A convenient and general method is proposed for the synthesis of 5\*-nucleotide phosphonate analogs starting from 5-deoxy-1,2-0isopropylidene-d-D-xylo-hexofuranose (I).