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 

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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