HERON Rearrangement (Heteroatom Rearrangements on )
J. M. Buccigross et al., Aust. J. Chem. 48, 353 (1995); J. M. Buccigross, S. A. Glover, J. Chem. Soc. Perkin Trans. II
Henry Reaction (Nitroaldol Reaction)
L. Henry, Compt. Rend. 120, 1265 (1895); J. Kamlet, US 2151517 (1939).
Base-catalyzed aldol-type condensation, q.v.
Helferich Method
B. Helferich, E. Schmitz-Hillebrecht, Ber. 66, 378 (1933).
Glycosidation of an acetylated sugar by heating with a phenol in the presenc
Heck Reaction
R. F. Heck, J. P. Nolley, Jr., J. Org. Chem. 37, 2320 (1972).
Stereospecific palladium-catalyzed coupling of alkenes with organic halides
Hayashi Rearrangement
M. Hayashi, J. Chem. Soc. 1927, 2516; 1930, 1513, 1520, 1524.
Rearrangement of o-benzoylbenzoic acids in the presence of sulfuric
Haworth Synthesis
R. D. Haworth, J. Chem. Soc. 1932, 1125, 2717, idem et al., ibid. 1784, 2248, 2720; 1934, 454.
Preparation of phenanthrenes from naph
Haworth Methylation
W. N. Haworth, J. Chem. Soc. 107, 13 (1915).
Formation of methylated methyl glycosides from monosaccharides with dimethyl sulfate an
Harries Ozonide Reaction (Ozonolysis)
C. Harries, Ann. 343, 311 (1905).
Treatment of olefins with ozone as a method of cleaving olefinic linkages. On hy
Lieben Iodoform Reaction (Haloform Reaction)
A. Lieben, Ann. (Suppl.) 7, 218 (1870).
Cleavage of methyl ketones with halogens (mostly iodine) and base t
Koch-Haaf Carboxylations
H. Koch, Brennstoff Chem. 36, 321 (1955); H. Koch, W. Haaf, Ann. 618, 251 (1958).
Formation of tertiary carboxylic acids by tre
Vilsmeier-Haack Reaction
A. Vilsmeier, A. Haack, Ber. 60, 119 (1927).
Formylation of activated aromatic or heterocyclic compounds with disubstituted for
