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19 results on '"Wiemer DF"'

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1. Diester Prodrugs of a Phosphonate Butyrophilin Ligand Display Improved Cell Potency, Plasma Stability, and Payload Internalization.

2. Efficiency of bis-amidate phosphonate prodrugs.

3. Incorporation of a FRET pair within a phosphonate diester.

4. Novel benzimidazole phosphonates as potential inhibitors of protein prenylation.

5. Stability and Efficiency of Mixed Aryl Phosphonate Prodrugs.

6. Phosphinophosphonates and Their Tris-pivaloyloxymethyl Prodrugs Reveal a Negatively Cooperative Butyrophilin Activation Mechanism.

7. Evaluation of a 7-Methoxycoumarin-3-carboxylic Acid Ester Derivative as a Fluorescent, Cell-Cleavable, Phosphonate Protecting Group.

8. Prodrugs of phosphonates and phosphates: crossing the membrane barrier.

9. Synthesis and reactivity of alkyl-1,1,1-trisphosphonate esters.

10. Direct conversion of benzylic and allylic alcohols to phosphonates.

11. Alpha-phosphono lactone analogues of cytidine and cytosine arabinoside diphosphates: synthesis via ring closing metathesis.

12. Synthesis of 5'-amino-5'-phosphonate analogues of pyrimidine nucleoside monophosphates.

13. Stereoselective synthesis of the 5'-hydroxy-5'-phosphonate derivatives of cytidine and cytosine arabinoside.

14. Alpha-phosphono lactone analogues of farnesyl pyrophosphate: an asymmetric synthesis via ring-closing metathesis.

15. Preparation of alpha-phosphono lactams via electrophilic phosphorus reagents: an application in the synthesis of lactam-based farnesyl transferase Inhibitors.

16. Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside.

17. Phosphonate and bisphosphonate analogues of farnesyl pyrophosphate as potential inhibitors of farnesyl protein transferase.

18. Stereochemistry-dependent inhibition of RAS farnesylation by farnesyl phosphonic acids.

19. Cyclic (1R,3R)-1,3-dimethyltrimethylene [(5R)-2-hydroxy-5-methyl-5-(2- methyl-1,3-dioxolan-2-yl)-1-cyclohexen-1-yl]-phosphonate, a stable enol.

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