de Mayo Reaction
P. de Mayo et al., Proc. Chem. Soc. London 1962, 119; P. de Mayo, H. Takeshita, Can. J. Chem. 41, 440 (1963).
Synthesis of 1,5-diketone
Darzens-Nenitzescu Synthesis of Ketones
G. Darzens, Compt. Rend. 150, 707 (1910); C. D. Nenitzescu, I. P. Cantuniari, Ann. 510, 269 (1934); C. D. Nenitzescu, C. Cioranescu
Dakin Reaction
H. D. Dakin, Am. Chem. J. 42, 477 (1909).
Replacement of the formyl or acetyl groups in phenolic aldehydes or ketones by a hydroxyl group
Kolbe Electrolytic Synthesis; Crum Brown-Walker Reaction
H. Kolbe, Ann. 69, 257 (1849).
Formation of symmetrical dimers by the electrolysis of carboxyla
Friedel-Crafts Reaction
C. Friedel, J. M. Crafts, Compt. Rend. 84, 1392, 1450 (1877).
The alkylation or acylation of aromatic compounds catalyzed by alu
Perkin Rearrangement (Coumarin-Benzofuran Ring Contraction)
W. H. Perkin, J. Chem. Soc. 23, 368 (1870).
Formation of benzofuran-2-carboxylic acids and b
Cornforth Rearrangement
J. W. Cornforth, The Chemistry of (Princeton University Press, New Jersey, 1949) p 700.
Thermal rearrangement of 4-carbonyl sub
Corey-Winter Olefin Synthesis
E. J. Corey, R. A. E. Winter, J. Am. Chem. Soc. 85, 2677 (1963).
Synthesis of olefins from 1,2-diols and thiocarbonyldiimi
Corey-Kim Oxidation
E. J. Corey, C. U. Kim, J. Am. Chem. Soc. 94, 7586 (1972).
Oxidation of primary and secondary alcohols via their alkoxysulfonium sal
Cope Rearrangement; Oxy-Cope Rearrangement
A. C. Cope et al., J. Am. Chem. Soc. 62, 441 (1940).
Highly stereoselective [3,3]-sigmatropic rearrangement o
Cope Elimination Reaction
A. C. Cope et al., J. Am. Chem. Soc. 71, 3929 (1949); idem et al., ibid. 75, 3212 (1953).
Formation of an olefin and a hydroxy
Sandmeyer Reaction; Gattermann Reaction; Körner-Contardi Reaction
T. Sandmeyer, Ber. 17, 1633, 2650 (1884); L. Gattermann, Ber. 23, 1218 (1890); G. Körner, A. Co
