- Cannizzaro Reaction
-
Cannizzaro Reaction
S. Cannizzaro, Ann. 88, 129 (1853); K. List, H. Limpricht, Ann. 90, 180 (1854).
Base-catalyzed disproportionation reaction of aromatic or aliphatic aldehydes with no α-hydrogen to corresponding acid and alcohol. If the aldehydes are different, the reaction is called the “crossed Cannizarro reaction”:

T. A. Geissman, Org. React. 2, 94 (1944); F. P. B. Van der Maeden et al., Rec. Trav. Chim. Pays-Bas 91(2), 221 (1972); C. G. Swain et al., J. Am. Chem. Soc. 101, 3576 (1979); R. S. McDonald, C. E. Sibley, Can. J. Chem. 59, 1061 (1981). Review: T. Lane, A. Plagens, Named Organic Reactions (John Wiley & Sons, Chichester, 1998) p 40-42. Cf. Meerwein-Ponndorf-Verley Reduction; Oppenauer Oxidation; Tishchenko Reaction.
Prev: Hofmann Isonitrile Synthesis
Next: Camps Quinoline Synthesis - 【Back】【Close 】【Print】【Add to favorite 】
-
Health and Chemical more >
-
Hot Products
- 12604-92-1 Nickel alloy,base,Ni,Fe,Mn (Nimalloy)
- 571-44-8 4-Androsten-3b-ol-17-one
- 91-68-9 3-Diethylaminophenol
- 4238-84-0 d-LYSERGIC ACID DIMETHYLAMIDE
- 156192-32-4 Z-LEU-ARG-7-AMINO-4-METHYLCOUMARIN
- 131595-16-9 Tinolux BBS
- 27214-00-2 Glycerol phosphate calcium salt
- 76095-16-4 Enalapril maleate
- 16096-31-4 1,6-Hexanediol diglycidyl ether
- 182410-00-0 Beta-cyclodextrin Sulfobutyl Ether Sodium
- 67922-59-2 Oxirane, ethyl-, polymer with oxirane, monodecyl ether (EO 10 mol and BO 1,5 mol)
- 1530-32-1 Ethyltriphenylphosphonium bromide


