Dr Chris A Russell

Chemistry

1. Heterocyclic Compound 100%
2. Oxidative Addition 80%
3. Phosphorus 80%
4. Transition Metal 61%
5. Chemistry 60%
6. Borane 60%
7. Ambient Reaction Temperature 56%
8. NMR Spectroscopy 50%
9. Ethylene 40%
10. Carbonylation 40%
11. Biphenylene 40%
12. formation 40%
13. pre-catalyst 40%
14. dimer 35%
15. Biaryl 33%
16. Reductive Elimination Reaction 30%
17. Selenium 30%
18. Biphenyl 30%
19. Crystal Structure 30%
20. Density Functional Theory 30%
21. Table Salt 30%
22. Alkene 26%
23. aromaticity 26%
24. Kinetic Isotope Effect 20%
25. Titanocene 20%
26. Hydroboration 20%
27. Diborane(4) 20%
28. N-Heterocyclic Carbene 20%
29. Coordination Chemistry 20%
30. Thermal Stability 20%
31. Transmetalation 20%
32. Ring Expansion 20%
33. Diastereomer 20%
34. Dehydrogenation 20%
35. Cleavage 20%
36. Phosphonium 20%
37. Carbene 20%
38. Lithium 20%
39. Metallocene 20%
40. Triple Bond 20%
41. Tin 20%
42. Electron Donor 20%
43. Styrene 20%
44. Sulfuration 20%
45. Moessbauer Spectroscopy 20%
46. Hydrogen 20%
47. X-Ray Crystallography 20%
48. Borazine 20%
49. Pnictogen 20%
50. Cyclopentadienyl 20%