P-chiral phosphorothioate analogs of thymidine and adenosine nucleotides are transformed in high yield with retention of configuration by [180]chloral and [l80]styrene oxide into corresponding nucleoside [l\*O]phosphates. It has been shown in our recent reports that 18 0-labelled reagents such as di
โฆ LIBER โฆ
The stereospecific conversion of P-chiral dialkyl phosphorothioates into [18O]-phosphates
โ Scribed by Paul M. Cullis
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 211 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
S-&thy1 thymidine (SP)-3',5'-cyclic phosphorothioate and S-methyl 5'-O+hyaudyl 3'thymidyl (Rp)-phosphorothioate are readily converted by means of sodium ["Ol-hydroxide into the corresponding ["Ol-phosphate diesters stereospecifically with retention of configuration at phosphorus.
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