102 results on '"Smith, L. H."'
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2. Ten Generations of Corn Breeding
3. Seed Development, Metabolism, and Composition
4. Method 2: Reduction of Esters
5. Method 1: Hydration of Carbonyl Compounds
6. Method 1: Synthesis Using Single-Electron-Transfer Reagents
7. Method 2: Acylation of Ketones
8. Method 3: Synthesis from 1-Acyloxy-1-hydroxy Compounds, Carbonyl Hydrates, or Vinyl Esters
9. Variation 1: Using a Lewis Acid Catalyst
10. Variation 2: Oxidation of Furan Derivatives
11. Method 6: Deprotection of Protected Cyclic Hemiacetals
12. Variation 1: Deprotection of -Alkyl Lactols
13. Product Subclass 3: Carbonyl Hydrates
14. Variation 3: Other Oxidations
15. Variation 2: In the Absence of a Catalyst
16. Method 8: Oxidation of Cyclic Ethers
17. Alkylation of Carboxy Groups
18. Method 3: Oxidation of Diols
19. Method 1: Synthesis Using Hal/Hal Acetal Electrophiles
20. Variation 2: Oxidation Using Selenium Dioxide
21. Method 1: Reduction of Lactones
22. Variation 2: Deprotection of -Acyl Lactols
23. Product Subclass 2: Lactols
24. Variation 3: By Selective Oxidation of Allylic and Benzylic Hydroxy Groups
25. Variation 2: By Selective Oxidation of a Secondary Hydroxy Group
26. Method 2: Addition of Carbon Nucleophiles to Lactones
27. Variation 2: Addition of Nucleophiles Bearing Stabilizing Groups to Esters Bearing Stabilizing Groups
28. Variation 4: Using Borohydride Reagents
29. Oxidative Methods
30. Variation 1: By Selective Oxidation of a Primary Hydroxy Group
31. Method 1: Synthesis from Aldehydes or Ketones by Addition of Alcohols
32. Variation 1: Acid-Catalyzed Hydration of Enol Ethers
33. Variation 1: Oxidation of Benzylic Methyl and Methylene Groups
34. Method 1: Acylation of Aldehydes
35. Variation 3: Synthesis from Strained Ketones
36. Acylation of Carbonyl Compounds
37. Method 5: Addition of Carbon Nucleophiles to Dicarbonyl Compounds
38. Variation 3: Metal Hydride Catalyzed Hydrosilylation
39. Variation 1: Synthesis of Meldrum’s Acid Using a Diacid and a Ketone
40. Method 2: Oxidation of Activated Methyl or Methylene Groups
41. Method 2: Synthesis Using O/Hal Acetal Electrophiles
42. Variation 1: Synthesis from Carbonyl Compounds Bearing Electron-Withdrawing Groups
43. Variation 1: Oxidation Using Dimethyldioxirane
44. Synthesis of Product Class 18
45. Synthesis from Propargyl Esters
46. Variation 1: Addition of Nucleophiles Bearing Stabilizing Groups
47. Method 7: Synthesis From Enol Ethers
48. Variation 2: Using an Oxo Acid
49. Synthesis of Product Subclass 2
50. Variation 3: Deprotection of -Silyl Lactols
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