Tiemann Rearrangement F. Tiemann, Ber. 24, 4162 (1891). Rearrangement of amide oximes (available from nitriles and hydroxylamine) to monosubstituted ure

Ziegler Method (Thorpe-Ziegler Method) K. Ziegler et al., Ann. 504, 94 (1933). Cyclization of dinitriles at high dilution in dialkyl ether in the presen

Thorpe Reaction H. Baron, et al., J. Chem. Soc. 85, 1726 (1904); K. Ziegler et al., Ann. 504, 94 (1933). Base-catalyzed self-condensation of nitriles to

Thiele Reaction (Thiele-Winter Acetoxylation) J. Thiele, Ber. 31, 1247 (1898). Formation of triacetoxy aromatic compounds by the reaction of quinones wi

Tafel Rearrangement J. Tafel, H. Hahl, Ber. 40, 3312 (1907). Rearrangement of the carbon skeleton of substituted acetoacetic esters to hydrocarbons with

Swarts Reaction F. Swartx, Bull. Acad. Roy. Belg. 24, 309 (1892). Fluorination of organic polyhalides with antimony trifluoride (or zinc and mercury flu

Suzuki Coupling N. Miyaura et al., Tetrahedron Letters 1979, 3437; N. Miyaura, A. Suzuki, Chem. Commun. 1979, 866. -catalyzed cross coupling of organic

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