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
Sarett Oxidation; Collins Oxidation
G. I. Poos, G. E. Arth, R. E. Beyler, L. H. Sarett, J. Am. Chem. Soc. 75, 422 (1953).
Oxidation of primary and secon
Clemmensen Reduction
E. Clemmensen, Ber. 46, 1837 (1913); 47, 51, 681 (1914).
Reduction of carbonyl groups of aldehydes and ketones to methylene groups
Claisen Rearrangement; Eschenmoser-Claisen Rearrangement; Johnson-Claisen Rearrangement; Ireland-Claisen Rearrangement
L. Claisen, Ber. 45, 3157 (1912); L. Claisen, E. Tie
