Nuno Maulide

Chemistry

1. Carboxamide 100%
2. Chemoselectivity 54%
3. Arylation 50%
4. Alkene 39%
5. formation 36%
6. Umpolung 36%
7. Sulfonium 34%
8. Nucleophile 33%
9. Ylide 28%
10. Sulfoxide 26%
11. Cycloaddition 26%
12. Alkyne 26%
13. amination 26%
14. Ynamide 24%
15. Ketones 23%
16. Enolates 19%
17. Allylic Alkylation 17%
18. cyclopropanation 17%
19. Carbonyl Compound 16%
20. Electrophile 16%
21. Palladium 16%
22. Chirality 16%
23. Carbocation 15%
24. Lactone 15%
25. Heterocyclic Compound 14%
26. Sulfur Ylide 14%
27. Bronsted Acid 14%
28. Thioester 13%
29. Carboxylic Acid 13%
30. Ring Opening Reaction 13%
31. Cyclobutene 12%
32. stability 12%
33. olefination 12%
34. Enantiomer 11%
35. Protecting Groups 10%
36. Stereoselectivity 10%
37. Mechanistic Study 10%
38. Transition Metal 10%
39. Enamide 10%
40. Triflate 10%
41. Lewis Base 10%
42. Alkylation 9%
43. Selenium 9%
44. Carbonyl Group 9%
45. Ketone 9%
46. Enantioselectivity 9%
47. Isomerization 8%
48. Pyrone 8%
49. Diastereoselectivity 8%
50. Allene 8%