List Of Name Reactions in Organic Chemistry With Mechanism

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z 

List of Name Reactions in Chemistry

A

  1. Acetoacetic-Ester Synthesis
  2. Acetoacetic-Ester Condensation (Claisen Condensation)
  3. Appel Reaction
  4. Acyloin Condensation
  5. Alder (Ene) Reaction (Hydro-Allyl Addition)
  6. Aldol Reaction
  7. Alkene (Olefin) Metathesis
  8. Alkyne Metathesis
  9. Amadori Reaction/Rearrangement
  10. Arbuzov Reaction (Michaelis-Arbuzov Reaction)
  11. Arndt-Eistert Homologation/Synthesis
  12. Aza-Claisen Rearrangement
  13. Aza-Cope Rearrangement
  14. Aza-Wittig Reaction
  15. Aza-[2,3]-Wittig Rearrangement
  16. Alkylation Enyne Metathesis.

B

  1. Baeyer-Villiger Oxidation/Rearrangement
  2. Baker-Venkataraman Rearrangement
  3. Baldwin’s Rules/Guidelines for Ring-Closing Reactions
  4. Balz-Schiemann Reaction (Schiemann Reaction)
  5. Bamford-Stevens-Shapiro Olefination
  6. Barbier Coupling Reaction
  7. Bartoli Indole synthesis
  8. Barton Nitrite Ester Reaction
  9. Barton Radical Decarboxylation Reaction
  10. Barton-McCombie Radical Deoxygenation Reaction
  11. Baylis-Hillman Reaction Beckmann Rearrangement
  12. Beckmann Rearrangement
  13. Benzilic Acid Rearrangement
  14. Benzoin and Retro-Benzoin Condensation
  15. Bergman Cycloaromatization Reaction
  16. Biginelli Reaction.
  17. Birch Reduction.
  18. Bischler-Napieralski Isoquinoline Synthesis
  19. Brook Rearrangement
  20. Brown Hydroboration Reaction
  21. Buchner Method of Ring Expansion (Buchner Reaction)
  22. Buchwald-Hartwig Cross-Coupling
  23. Burgess Dehydration Reaction

C

  1. Cannizzaro Reaction
  2. Carroll Rearrangement (Kimel-Cope Rearrangement)
  3. Castro-Stephens Coupling
  4. Chichibabin Amination Reaction (Chichibabin Reaction)
  5. Chugaev Elimination Reaction (Xanthate Ester Pyrolysis)
  6. Ciamician-Dennstedt Rearrangement
  7. Claisen Condensation/Claisen Reaction
  8. Claisen Rearrangement
  9. Claisen-Ireland Rearrangement
  10. Clemmensen Reduction
  11. Combes Quinoline Synthesis
  12. Cope Elimination / Cope Reaction
  13. Cope Rearrangement
  14. Corey-Bakshi-Shibata Reduction (CBS Reduction)
  15. Corey-Chaykovsky Epoxidation and Cyclopropanation
  16. Corey-Fuchs Alkyne Synthesis
  17. Corey-Kim Oxidation
  18. Corey-Nicolaou Macrolactonization
  19. Corey-Winter Olefination Cornforth Rearrangement
  20. Criegee Oxidation
  21. Curtius Rearrangement

D

  1. Dakin Oxidation
  2. Dakin-West Reaction
  3. Danheiser Benzannulation
  4. Danheiser Cyclopentene Annulation
  5. Danishefsky’s Diene Cycloaddition
  6. Darzens Glycidic Ester Condensation
  7. Davis’ Oxaziridine Oxidations
  8. De Mayo Cycloaddition (Enone-Alkene [2+2] Photocycloaddition)
  9. Demjanov Rearrangement and Tiffeneau-Demjanov Rearrangement
  10. Dess-Martin Oxidation
  11. Dieckmann Condensation
  12. Diels-Alder Cycloaddition
  13. Dienone-Phenol Rearrangement
  14. Dimroth Rearrangement
  15. Doering-LaFlamme Allene Synthesis
  16. Dötz Benzannulation Reaction Enders SAMP/RAMP Hydrazone

E

  1. Eschenmoser Methenylation
  2. Eschenmoser-Claisen Rearrangement
  3. Eschenmoser-Tanabe Fragmentation
  4. Eschweiler-Clarke Methylation (Reductive Alkylation)
  5. Evans Aldol Reaction

F

  1. Favorskii and Homo-Favorskii Rearrangement
  2. Favorskii Rearrangement
  3. Feist-Bénary Furan Synthesis Ferrier Reaction/Rearrangement
  4. Finkelstein Reaction
  5. Fischer Indole Synthesis
  6. Fleming-Tamao Oxidation
  7. Friedel-Crafts Acylation
  8. Friedel-Crafts Alkylation
  9. Fries-, Photo-Fries, and Anionic Ortho-Fries Rearrangement

G

  1. Gabriel Synthesis
  2. Gattermann and Gattermann-Koch Formylation
  3. Glaser Coupling
  4. Grignard Reaction
  5. Grob Fragmentation

H

  1. Hajos-Parrish Reaction
  2. Hantzsch Dihydropyridine Synthesis
  3. Heck Reaction
  4. Heine Reaction.
  5. Hell-Volhard-Zelinsky Reaction
  6. Henry Reaction
  7. Hetero Diels-Alder Cycloaddition (HDA)
  8. Hofmann Elimination
  9. Hofmann-Löffler-Freytag Reaction (Remote Functionalization)
  10. Hofmann Rearrangement
  11. Horner-Wadsworth-Emmons Olefination
  12. Horner-Wadsworth-Emmons Olefination – Still-Gennari Modification
  13. Houben-Hoesch Reaction/Synthesis
  14. Hunsdiecker Reaction

J

  1. Jacobsen Hydrolytic Kinetic Resolution
  2. Jacobsen-Katsuki Epoxidation
  3. Japp-Klingemann Reaction
  4. Johnson-Claisen Rearrangement
  5. Jones Oxidation/Oxidation of Alcohols by Chromium Reagents
  6. Julia-Lythgoe Olefination.

K

  1. Kagan-Molander Samarium Diiodide-Mediated Coupling
  2. Kahne Glycosidation
  3. Keck Asymmetric Allylation
  4. Keck Macrolactonization
  5. Keck Radical Allylation
  6. Knoevenagel Condensation Knorr Pyrrole Synthesis
  7. Koenigs-Knorr Glycosidation
  8. Kolbe-Schmitt Reaction
  9. Kornblum Oxidation
  10. Krapcho Dealkoxycarbonylation (Krapcho reaction)
  11. Kröhnke Pyridine Synthesis
  12. Kulinkovich Reaction
  13. Kumada Cross-Coupling
  14. Larock Indole Synthesis

L

  1. Ley Oxidation
  2. Lieben Haloform Reaction
  3. Lossen Rearrangement
  4. Luche Reduction

M

  1. Madelung Indole Synthesis
  2. Malonic Ester Synthesis
  3. Mannich Reaction
  4. McMurry Coupling
  5. Meerwein Arylation
  6. Meerwein-Ponndorf-Verley Reduction
  7. Meisenheimer Rearrangement
  8. Meyer-Schuster and Rupe Rearrangement
  9. Michael Addition Reaction
  10. Midland Alpine Borane Reduction
  11. Minisci Reaction
  12. Mislow-Evans Rearrangement
  13. Mitsunobu Reaction
  14. Miyaura Boration
  15. Mukaiyama Aldol Reaction
  16. Myers Asymmetric Alkylation

N

  1. Nagata Hydrocyanation
  2. Nazarov Cyclization
  3. Neber Rearrangement
  4. Nef Reaction
  5. Negishi Cross-Coupling
  6. Nenitzescu Indole Synthesis
  7. Nicholas Reaction
  8. Noyori Asymmetric Hydrogenation
  9. Nozaki-Hiyama-Kishi Reaction

O

  1. Oppenauer Oxidation
  2. Overman Rearrangement
  3. Oxy-Cope Rearrangement
  4. Anionic Oxy-Cope Rearrangement

P

  1. Paal-Knorr Furan Synthesis
  2. Paal-Knorr Pyrrole Synthesis
  3. Passerini Multicomponent Reaction
  4. Paterno-Büchi Reaction
  5. Pauson-Khand Reaction
  6. Payne Rearrangement
  7. Perkin Reaction
  8. Petasis Boronic Acid-Mannich Reaction
  9. Petasis-Ferrier Rearrangement
  10. Peterson Olefination
  11. Pfitzner-Moffatt Oxidation
  12. Pictet-Spengler Tetrahydroisoquinoline Synthesis
  13. Pinacol and Semi-pinacol Rearrangement
  14. Pinner Reaction
  15. Pinnick Oxidation
  16. Polonovski Reaction
  17. Pomeranz-Fritsch Reaction
  18. Prévost Reaction
  19. Prilezhaev Reaction
  20. Prins Reaction
  21. Prins-Pinacol Rearrangement
  22. Pummerer Rearrangement

Q

  1. Quasi-Favorskii Rearrangement

R

  1. Ramberg-Bäcklund Rearrangement
  2. Reformatsky Reaction
  3. Regitz Diazo Transfer
  4. Reimer-Tiemann Reaction
  5. Riley Selenium Dioxide Oxidation
  6. Ritter Reaction
  7. Robinson Annulation
  8. Roush Asymmetric Allylation
  9. Rubottom Oxidation

S

  1. Saegusa Oxidation
  2. Sakurai Allylation
  3. Sandmeyer Reaction
  4. Schmidt Reaction
  5. Schotten-Baumann Reaction
  6. Schwartz Hydrozirconation
  7. Seyferth-Gilbert Homologation
  8. Sharpless Asymmetric Aminohydroxylation
  9. Sharpless Asymmetric Dihydroxylation
  10. Sharpless Asymmetric Epoxidation.
  11. Shi Asymmetric Epoxidation
  12. Simmons-Smith Cyclopropanation
  13. Skraup and Doebner-Miller Quinoline Synthesis
  14. Smiles Rearrangement
  15. Smith-Tietze Multicomponent Dithiane Linchpin Coupling
  16. Snieckus Directed Ortho Metalation
  17. Sommelet-Hauser Rearrangement
  18. Sonogashira Cross-Coupling
  19. Staudinger Ketene Cycloaddition
  20. Staudinger Reaction
  21. Stephen Aldehyde Synthesis (Stephen Reduction)
  22. Stetter Reaction
  23. Stevens Rearrangement
  24. Stille Carbonylative Cross-Coupling
  25. Stille Cross-Coupling (Migita-Kosugi-Stille Coupling)
  26. Stille-Kelly Coupling
  27. Stobbe Condensation
  28. Stork Enamine Synthesis
  29. Strecker Reaction
  30. Suzuki Cross-Coupling (Suzuki-Miyaura Cross-Coupling
  31. Swern Oxidation

T

  1. Takai-Utimoto Olefination (Takai Reaction)
  2. Tebbe Olefination/Petasis-Tebbe Olefination
  3. Tishchenko Reaction
  4. Tsuji-Trost Reaction/Allylation
  5. Tsuji-Wilkinson Decarbonylation Reaction

U

  1. Ugi Multicomponent Reaction
  2. Ullmann Biaryl Ether and Biaryl Amine Synthesis
  3. Ullmann Reaction/Coupling/Biaryl Synthesis

V

  1. Vilsmeier-Haack Formylation
  2. Vinylcyclopropane-Cyclopentene Rearrangement
  3. Von Pechman Reaction

W

  1. Wacker Oxidation
  2. Willgerodt-Kindler Reaction
  3. Wagner-Meerwein Rearrangement
  4. Weinreb Ketone Synthesis
  5. Wharton Fragmentation
  6. Wharton Olefin Synthesis (Wharton Transposition)
  7. Williamson Ether Synthesis
  8. Wittig Reaction
  9. Wittig Reaction – Schlosser Modification
  10. Wittig-[1,2]- and [2,3]-Rearrangement
  11. Wohl-Ziegler Bromination
  12. Wolff Rearrangement
  13. Wolff-Kishner Reduction

References :

  1. Name Reactions A Collection of Detailed Reaction Mechanisms By Jie Jack Li · 2013
  2. Name Reactions and Reagents in Organic Synthesis Bradford P. Mundy, Michael G. Ellerd, Frank G. Favaloro, Jr. · 2005
  3. Named Organic Reactions By Thomas Laue, Andreas Plagens · 2005
  4. Name Reactions – Organic Chemistry Portal
  5. Name reaction – Wikipedia
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All A-Z Name Reactions

Related Topic- All Reagents and there Use with mechanism and Examples

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