Synthesis of N -Phosphonamidothionate Derivatives of Glutamic Acid
β Scribed by Lu, Haiyan; Mlodnosky, Karyn L.; Dinh, Trang T.; Dastgah, Azar; Lam, Vinh Q.; Berkman, Clifford E.
- Book ID
- 126165790
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 56 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
The acquisition of the individual stereoisomers of chiral phosphonothioic acids is anticipated to reveal the significance of phosphorus stereochemistry upon the inhibition of metallocarboxypeptidases as well as their utility as chiral and stereoselective inhibitory probes. Two methods for preparing
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Novel aryl Nβphosphonamidothionate derivatives of nucleosides as membraneβsoluble prodrugs of bioactive free nucleotides have been prepared by phosphochloridothioate chemistry. Unprotected nucleosides, for example uridine and adenosine, were used; phosphorylation took place selectively