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  • Janovsky Reaction
  • Janovsky Reaction J. V. Janovsky, L. Erb, Ber. 19, 2155 (1886). Reaction of aldehydes and ketones containing α-methylene groups with m-dinitrobenz
  • Jacobsen Rearrangement
  • Jacobsen Rearrangement O. Jacobsen, Ber. 19, 1209 (1886); 20, 901 (1887). Reaction of polymethylbenzenes with concentrated sulfuric acid to give rearran
  • Jacobsen Epoxidation
  • Jacobsen Epoxidation W. Zhang et al., J. Am. Chem. Soc. 112, 2801 (1990); E. N. Jacobsen et al. ibid. 113, 7063 (1991). Chiral (salen)manganese(III)-cat
  • Ivanov Reaction
  • Ivanov Reaction D. Ivanov, A. Spassoff, Bull. Soc. Chim. France 49, 19, 375 (1931); D. Ivanov et al., ibid. 51, 1321, 1325, 1331 (1932). The addition o
  • Purdie Methylation
  • Purdie Methylation (Irvine-Purdie Methylation) T. Purdie, J. C. Irvine, J. Chem. Soc. 83, 1021 (1903). Exhaustive methylation of a methyl glycoside by r
  • Oxo Process
  • Oxo Process (Hydroformylation Reaction) O. Roelen, US 2327066 (1943); R. H. Hasek (Eastman), Org. Chem. Bull. 27, No. 1 (1955). Formation of alcohols fr
  • Hydroboration Reaction
  • Hydroboration Reaction H. C. Brown, B. C. Subba Rao, J. Am. Chem. Soc. 78, 5694 (1956); J. Org. Chem. 22, 1135, 1136 (1957). Addition of boron hydrides
  • Pictet-Hubert Reaction
  • Pictet-Hubert Reaction; Morgan-Walls Reaction A. Pictet, A. Hubert, Ber. 29, 1182 (1896); C. T. Morgan, L. P. Walls, J. Chem. Soc. 1931, 2447; 1932, 2225.
  • Wolff-Kishner Reduction
  • Wolff-Kishner Reduction; Huang-Minlon Modification N. Kishner, J. Russ. Phys. Chem. Soc. 43, 582 (1911), C.A. 6, 347 (1912); L. Wolff, Ann. 394, 86 (1912); Huang-Minlon, J
  • Houdry Cracking Process
  • Houdry Cracking Process E. Houdry, US 1957648 and US 1957649 (1934). Decomposition of or heavy petroleum fractions into more useful lower boiling mater
  • Sakurai Reaction
  • Sakurai Reaction (Hosomi-Sakurai Reaction) A. Hosomi, H. Sakurai, Tetrahedron Letters 1976, 1295; A. Hosomi et al., Chem. Letters 1976, 941. Lewis acid-
  • Hooker Reaction
  • Hooker Reaction S. C. Hooker, J. Am. Chem. Soc. 58, 1174 (1936). Oxidation of 2-hydroxy-3-alkyl-1,4-quinones with dilute alkaline permanganate with shor
  • Hofmann-Sand Reactions
  • Hofmann-Sand Reactions K. A. Hofmann, J. Sand, Ber. 33, 1340, 1353 (1900). Olefin mercuration with mercuric salts (halides, acetates, nitrates, or sulfa
  • Hofmann Reaction
  • Hofmann Reaction A. W. Hofmann, Ber. 14, 2725 (1881). Conversion of primary carboxylic amides to primary amines with one fewer carbon atom upon treatmen
  • Houben-Hoesch Reaction
  • Houben-Hoesch Reaction K. Hoesch, Ber. 48, 1122 (1915); J. Houben, ibid. 59, 2878 (1926). Synthesis of acylphenols from phenols or phenolic ethers by th
  • Nozaki-Hiyama Coupling Reaction
  • Nozaki-Hiyama Coupling Reaction (Nozaki-Hiyama-Kishi Reaction) Y. Okude et al., J. Am. Chem. Soc. 99, 3179 (1977); K. Takai et al., Tetrahedron Letters 24, 5281 (1983).
  • Hinsberg Synthesis of Thiophene Derivatives
  • Hinsberg Synthesis of Derivatives O. Hinsberg, Ber. 43, 901 (1910). Formation of thiophene carboxylic acids from α-diketones and dialkyl thiodiac
  • Hinsberg Sulfone Synthesis
  • Hinsberg Sulfone Synthesis O. Hinsberg, Ber. 27, 3259 (1894); 28, 1315 (1895). Formation of sulfonylquinol derivatives by addition of quinones to cold d
  • Hinsberg Oxindole and Oxiquinoline Synthesis
  • Hinsberg and Oxiquinoline Synthesis O. Hinsberg, Ber. 21, 110 (1888); 25, 2545 (1892); 41, 1367 (1908). Formation of oxindoles from secondary aryl amin
  • Hilbert-Johnson Reaction
  • Hilbert-Johnson Reaction T. B. Johnson, G. E. Hilbert, Science 69, 579 (1929); G. E. Hilbert, T. B. Johnson, J. Am. Chem. Soc. 52, 2001, 4489 (1930). Re
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