ke-Suhl Reaction T. Zincke, R. Suhl, Ber. 39, 4148 (1906). -dienone rearrangement of p-cresols by addition of carbon tetrachloride in the presence of al

Sugasawa Reaction T. Sugasawa et al., J. Am. Chem. Soc. 100, 4842 (1978); M. Adachi et al., Chem. Pharm. Bull. 33, 1826 (1985). Ortho acylation of anili

Suarez Reaction (Suarez Fragmentation) J. I. Concepion et al., Tetrahedron Letters 25, 1953 (1984); eidem, J. Org. Chem. 51, 402 (1986). Photoinduced co

Strecker Sulfite Alkylation A. Strecker, Ann. 148, 90 (1868). Formation of alkyl sulfonates by reaction of alkyl halides with alkali or ammonium sulfite

Strecker Degradation A. Strecker, Ann. 123, 363 (1862). Interaction of an α-amino acid with a carbonyl compound in aqueous solution or suspension

Strecker Amino Acid Synthesis A. Strecker, Ann. 75, 27 (1850); 91, 349 (1854). Synthesis of α-amino acids by reaction of aldehydes with ammonia an

Stork Enamine Reaction G. Stork et al., J. Am. Chem. Soc. 76, 2029 (1954); G. Stork, H. Landesman, ibid. 78, 5128 (1956). Synthesis of α-alkyl or

StolléSynthesis R. Stollé, Ber. 46, 3915 (1913); 47, 2120 (1914); J. Prakt. Chem. 105, 137 (1923); 128, 1 (1930). Formation of indole deri

Widman-Stoermer Synthesis O. Widman, Ber. 17, 722 (1884); R. Stoermer, H. Fincke, Ber. 42, 3115 (1909). Synthesis of cinnolines by cyclization of diazot

Stobbe Condensation H. Stobbe, Ber. 26, 2312 (1893); Ann. 282, 280 (1894). Condensation of aldehydes or ketones with diethyl succinate in the presence o

Stille Coupling M. Kosugi et al., Chem. Letters 1977, 301 (1977); D. Milstein, J. K. Stille, J. Am. Chem. Soc. 100, 3636 (1978). -catalyzed cross coupli

Stieglitz Rearrangement J. Stieglitz, P. N. Leech, Ber. 46, 2147 (1913); J. Am. Chem. Soc. 36, 272 (1914). Rearrangement of trityl hydroxylamines to Sch

Stevens Rearrangement T. S. Stevens et al., J. Chem. Soc. 1928, 3193; 1930, 2107, 2119; 1932, 55, 1926, 1932. Migration of an alkyl group from a sulfoni

Stephen Aldehyde Synthesis H. Stephen, J. Chem. Soc. 127, 1874 (1925); T. Stephen, H. Stephen, ibid. 1956, 4695. Reaction sequence employed to convert n

Staudinger Reaction H. Staudinger, J. Meyer, Helv. Chim. Acta 2, 635 (1919). Synthesis of phosphazo compounds by the reaction of tertiary phosphines wit

Sommelet Reaction M. Sommelet, Compt. Rend. 157, 852 (1913); Bull. Soc. Chim. France [4] 23, 95 (1918). Preparation of aldehydes from aralkyl halides by

Smiles Rearrangement; Truce-Smiles Rearrangement A. A. Levi et al., J. Chem. Soc. 1931, 3264; W. J. Evans, S. Smiles, ibid. 1935, 181; 1936, 329. Intram

Skraup Reaction Z. H. Skraup, Ber. 13, 2086 (1880). Synthesis of quinolines from aromatic amines, glycerol, an oxidizing agent and sulfuric acid:

Simonis Chromone Cyclization E. Petschek, H. Simonis, Ber. 46, 2014 (1913). Formation of chromones from phenol and β-keto esters in the presence of

Simonini Reaction A. Simonini, Monatsh. 13, 320 (1892); 14, 81 (1893). The preparation of aliphatic esters by the reaction of the silver salt of a carbo