Handbook of Organic Name Reactions

[Updated in response to the reviews]1: Organic Reaction Mechanism1. Nucleophilic addition to carbon-heteroatoms multiple bonds2. Electrophilic addition to carbon-carbon multiple bonds3. Nucleophilic aliphatic substitution4. Nucleophilic aromatic substitution5. Electrophilic aliphatic, alkenyl and alkynyl substitution6. Electrophilic aromatic substitution reaction7. Elimination reaction2: Reactions of Aldehydes and Ketones1. Aldol condensation reaction1. Cross aldol condensation reaction2. Henry Nitro Aldol Condensation3. Intramolecular Aldol Condensation4. List–Barbas Asymmetric Aldol Reaction5. Mukaiyama aldol reaction2. Bamford-Stevens reaction3. Barton decarboxylation reaction4. Barbier reaction 5. Barbier In Situ Grignard Reaction 6. Baer–Fischer Amino Sugar Synthesis 7. Baylis-Hillman reaction 8. Benzoin condensation 9. Bischler–Napieralski reaction 10. Bouveault-Blanc reduction reaction 11. Brown Anti Aldol via B-enolate 12. Cannizzaro reaction13. Claisen ester condensation 14. Clemmensen reduction reaction 15. Ciamician C=O Photocoupling 16. Crimmins–Heathcock Chiral Anti (Syn) Aldols17. Cross- Cannizzaro reaction 18. Dakin reaction 19. Darzens reaction20. De Mayo C=C Photocycloaddition 21. Dieckmann condensation reaction 22. Fujiwara Arylation Carboxylation 23. Gattermann aldehyde synthesis 24. Gattermann-Koch reaction 25. Haller bauer reaction 26. Haloform reaction 27. Hell-Volhard-Zelinsky reaction 28. Hunsdiecker reaction 29. Hollemann Pinacol Synthesis 30. Julia–Colonna Asymmetric Epoxidation 31. Knoevenagel reaction 32. Kiliani–Fischer Sugar Homologation 33. Mannich reaction 34. Meerwein-Ponndorf-Verley reduction reaction 35. Michael addition reaction 36. Norrish type-I reaction 37. Norrish type-II reaction 38. Paterno buchi reaction 39. Perkin reaction 40. Peterson olefination 41. Prins Reaction 42. Reformatsky reaction 43. Riley Selenium Dioxide Oxidation44. Ruff–Fenton Aldose Degradation45. Robinson annulations reaction 46. Rosenmund reaction 47. Shapiro reaction 48. Stobbe condensation reaction 49. Stork Enamine Alkylation 50. Tabbe reaction 51. Tishchenko Reaction 52. Tollen’s Reaction 53. Vedejs Ketone Hydroxylation 54. Wittig reaction 55. Wolff-Kishner reduction reaction 3: Reaction of Alcohols1. Barton-Mccombie deoxygenation 2. Baeyer–Villiger Aromatic Tritylation 3. Corey winter olefin synthesis 4. Corey–Chan Synthesis 5. Gattermann synthesis reaction 6. Grieco Olefination reaction 7. Houben hoesch reaction 8. Kolbe schmitt reaction 9. Mitsunobu reaction 10. Moffatt oxidation reaction 11. Mukaiyama–Ueno Oxidation 12. Reimer-Tiemann reaction 13. Ritter reaction 14. Swern oxidation reaction15. Sharpless asymmetric epoxidation16. Sharpless Asymmetric Dihydroxylation17. Simmons–Smith Cyclopropanation 4: Reactions of Heterocyclic Compounds1. Algar flynn oyamada reaction 2. Bischler–Mohlau Indole Synthesis 3. Camps Quinoline Synthesis 4. Chichibabin reaction 5. Clauson–Kaas Pyrrole Synthesis 6. Combes Quinoline Synthesis 7. Dimroth Triazole Synthesis 8. Finegan Tetrazole Synthesis 9. Fischer Indole Synthesis 10. Hantzsch Pyrrole Synthesis 11. Hantzsch Thiazole Synthesis 12. Knorr Pyrrole Synthesis 13. Macdonald Porphyrin Synthesis 14. Madelung Indole Synthesis 15. Reissert Indole Synthesis 16. Pfitzinger Quinoline Synthesis 17. Pomeranz–Fritsch–Schlitter Isoquinoline Synthesis18. Skraup synthesis 5: Coupling Reactions 1. Alper Carbonylation2. Buchwald Hartwig Coupling3. Fukuyama Thioester Coupling4. Fűrstner Fe Catalyzed C=C Coupling 5. Glaser–Sondheimer Acetylene Coupling 6. Hiyama Coupling 7. Heck Coupling 8. Knochel Coupling 9. Kumada Coupling 10. Mcmurry Coupling 11. Morita–Baylis–Hillman 12. Negishi Coupling 13. Nozaki-Hiyama Reaction 14. Sonogashira Coupling 15. Stille Coupling 16. Suzuki Coupling 17. Suzuki–Miyaura 18. Stephens–Castro Acetylene Coupling 6: Rearrangements, Participation and Fragmentation Reactions 1. Arndt-Eistert Homologation 2. Amadori Glucosamine Rearrangement 3. Auwers–Inhoffen Dienone–Phenol Rearrangement 4. Baeyer-Villiger Oxidation Reaction 5. Beckmann Rearrangement 6. Benzidine Rearrangement 7. Benzil-benzillic acid rearrangement 8. Brook rearrangement 9. Sigmatropic rearrangements 1. Aza-Cope rearrangements 2. Claisen rearrangement 3. Cope rearrangement 4. Intramolecular Aldol Condensation 5. Ireland–Claisen rearrangement 6. Oxy-Cope rearrangements 10. Carroll Allyl B-Ketoester Rearrangement 11. Chan Acyloxyacetic Ester Rearrangement 12. Chapman Rearrangement 13. Curtius Rearrangement 14. Demjanov Diazonium Rearrangement 15. Eschenmoser fragmentation reaction 16. Favorskii rearrangement 17. Fittig Pinacol-Pinacolone rearrangement18. Fries rearrangement 19. Grob fragmentation 20. Hofmann rearrangement 21. Hofmann–Loffler Rearrangement 22. Lossen rearrangement 23. Nazarov cyclization 24. Neber Rearrangement 25. Photofries rearrangement 26. Pummerer rearrangement 27. Pschorr cyclization 28. Payne Rearrangement 29. Semipinacol rearrangement 30. Schmidt rearrangement 31. Smiles rearrangement 32. Sommelet-Hauser rearrangement 33. Stevens Rearrangement 34. Stieglitz and Related Rearrangements 35. Tiffeneau–Demyanov ring expansion 36. Tiffeneau Aminoalcohol Rearrangement 37. Von-Richter rearrangement 38. Wagner Meerwein rearrangement 39. Wittig Rearrangement 40. Wolff rearrangement 41. Zimmerman Di-Π Methane Rearrangement 7: Reaction of amines, carboxylic acid and derivatives 1. Arbuzov Synthesis2. Buchwald–Hartwig Amination3. Breckport B-Lactam Synthesis4. Bouveault–Blanc Ester Reduction 5. Chugaev reaction 6. Darapski Amino Acid Synthesis 7. Erlenmeyer–Bergmann Amino Acid Synthesis 8. Eschenmoser-Tanabe reaction 9. Gabriel Synthesis 10. Gabriel phthalimide reaction 11. Hofmann Quaternary Ammonium Elimination 12. Hofmann–Loeffler–Freytag Synthesis 13. Kametani Oxidation 14. Prelog–Stoll Acyloin Condensation 15. Pschorr Arylation 16. Reissert Reaction 17. Vilsmeier haack reaction 18. Sandmeyer–Gattermann reaction 19. Strecker Aminoacid Synthesis 20. Tamao–Fleming Hydroxylation 21. Weinreb Ketone Synthesis 8: Miscellaneous Reactions 1. Alder (Ene) Reaction 2. Anti-Markovnikov's Regioselectivity 3. Auwers Flavone Synthesis 4. Barton Reaction 5. Borsche–Beech Synthesis 6. Balson reaction 7. Birch reduction 8. Click (Fokin) Synthesis 9. Diels alder reaction 10. Dakin–West Ketone Synthesis 11. Darzens Epoxide Synthesis 12. Dutt–Wormall Azide Synthesis 13. Etard reaction 14. Fischer Carbene reaction 15. Felkin Cyclization 16. Fittig reaction 17. Friedel crafts alkylation reaction 18. Friedel crafts acylation reaction 19. Gomberg –Bachmann reaction 20. Grubbs Olefin Metathesis 21. Hauser–Beak Ortho Lithiation 22. Koch reaction 23. Kucherov–Deniges Hydration 24. Lemieux–Johnson reaction 25. Markovnikov's Regioselectivity 26. Nef reaction 27. Oppolzer Synthesis 28. Pauson–Khand Annulation 29. Petasis Titanocene Carbene Olefination 30. Peterson Olefination 31. Pfau–Plattner Synthesis 32. Prevost reaction 33. Prevost–Woodward reaction 34. Ramberg–Backlund Reaction 35. Simon smith reaction 36. Stephen reaction 37. Story synthesis 38. Sandmeyer reaction 39. Staudinger Cycloaddition 40. Stille Synthesis 41. Stork Radical Cyclization 42. Ullmann reaction 43. Williamson ether synthesis 44. Wurtz reaction 45. Wurtz fittig reaction