Gomberg-Bachmann Reaction
M. Gomberg, W. E. Bachmann, J. Am. Chem. Soc. 46, 2339 (1924).
Alkali dependent formation of diaryl compounds from aryl diazon
Favorskii-Babayan Synthesis
A. E. Favorskii, J. Russ. Phys. Chem. Soc. 37, 643 (1905); Chem. Zentr. 1905, II, 1018; A. Babayan et al., J. Gen. Chem. (USSR) 9, 1631 (1939).
Auwers Synthesis
K. v. Auwers et al., Ber. 41, 4233 (1908); 48, 85 (1915); 49, 809 (1916); K. v. Auwers, P. Pohl, Ann. 405, 243 (1914).
Expansion of cou
Arens-van Dorp Synthesis; Isler Modification
D. A. van Dorp, J. F. Arens, Nature 160, 189 (1947); J. F. Arens et al., Rec. Trav. Chim. 68, 604, 609 (1949); O. Isler et al.
Michaelis-Arbuzov Reaction
A. Michaelis, R. Kaehne, Ber. 31, 1048 (1898); A. E. Arbuzov, J. Russ. Phys. Chem. Soc. 38, 687 (1906); Chem. Zentr. 1906, II, 1639.
Hofmann-Martius Rearrangement ( Rearrangement)
A. W. Hofmann, C. A. Martius, Ber. 4, 742 (1871); A. W. Hofmann, ibid. 5, 720 (1872).
Thermal conversion
Meerwein-Ponndorf-Verley Reduction ( Alkoxide Reduction)
H. Meerwein, R. Schmidt, Ann. 444, 221 (1925); W. Ponndorf, Angew. Chem. 39, 138 (1926); A. Verley, Bull. Soc. Chi
Allylic Rearrangements
L. Claisen, Ber. 45, 3157 (1912).
Migration of a carbon-carbon double bond in a three carbon (allylic) system on treatment with n
Allan-Robinson Reaction
J. Allan, R. Robinson, J. Chem. Soc. 125, 2192 (1924).
Preparation of flavones or isoflavones by condensing o-hydroxyaryl ketone
Algar-Flynn-Oyamada Reaction
J. Algar, J. P. Flynn, Proc. Roy. Irish Acad. 42B, 1 (1934); B. Oyamada, J. Chem. Soc. Japan 55, 1256 (1934).
Alkaline hydr
Aldol Reaction (Condensation)
R. Kane, Ann. Phys. Chem., Ser. 2, 44, 475 (1838); idem, J. Prakt. Chem. 15, 129 (1838).
Traditionally, it is the acid- or
Ene Reaction (Alder-Ene Reaction); Conia Reaction
K. Alder et al., Ber. 76, 27 (1943).
The addition of an alkene having an allylic hydrogen (ene) to a c
Diels-Alder Reaction
O. Diels, K. Alder, Ann. 460, 98 (1928); 470, 62 (1929); Ber. 62, 2081, 2087 (1929).
The 1,4-addition of the double bond of a dieno
Michael Reaction (Addition, Condensation)
A. Michael, J. Prakt. Chem. [2] 35, 349 (1887).
Base-promoted conjugate addition of carbon nucleophiles (donor