22 results on '"Powell, William S."'
Search Results
2. A novel PGD 2 receptor expressed in eosinophils
3. Structure-activity relationship study of β-oxidation resistant indole-based 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) receptor antagonists
4. A convenient strategy for the synthesis of β,γ-unsaturated aldehydes and acids. A construction of skipped dienes
5. A new method for the preparation of olefins from vicinal diols
6. Stereoselective synthesis of two highly potent 5-oxo-ETE receptor antagonists
7. Base-dependent formation of cis and trans olefins and their application in the synthesis of 5-oxo-ETE receptor antagonists
8. C 20-trifluoro-5-oxo-ETE: A metabolically stable 5-oxo-ETE derivative
9. 5-Oxo-15-HETE: Total synthesis and bioactivity
10. A new approach to the synthesis of polyunsaturated deuterated isoprostanes: Total synthesis of d 4-5- epi-8,12- iso-iPF 3α-VI and d 4-8,12- iso-iPF 3α-VI
11. Eicosapentaenoic-acid-derived isoprostanes: Synthesis and discovery of two major isoprostanes
12. Synthesis of 15R-PGD 2: a potential DP 2 receptor agonist
13. iPF 2α-III-17,18,19,20- d4: Total synthesis and metabolism
14. A new synthetic approach for 4( S)-hydroxycyclopent-2-enone: a precursor to prostanoid synthesis
15. An efficient preparation of stereospecific β-hydroxy nitriles
16. Silyl group deprotection by Pd/C/H 2. A facile and selective method
17. An efficient approach to the synthesis of LTB 4 and ω-substituted LTB 4 metabolites
18. A photoaffinity probe for 5-hydroxyeicosanoid dehydrogenase suitable for radioiodination
19. The synthesis of a 5-HETE photoaffinity ligand
20. The design and synthesis of a 5-HETE affinity chromatography ligand for 5-hydroxyeicosanoid dehydrogenase
21. Intramolecular sulfur-assisted NaBH 4 reduction of esters synthesis of 5-oxo-ETE and 5-oxo-12-HETE
22. Total synthesis of proinflammatory dihydro-12-KETE metabolites
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.