Meyer Synthesis (Victor Meyer Synthesis)
V. Meyer, O. Stuber, Ber. 5, 203 (1872).
Formation of aliphatic nitrites and nitro derivatives by the reaction
Meyer Reaction
G. Meyer, Ber. 16, 1439 (1883).
Preparation of alkylstannonic acids by reacting alkali stannite with an alkyl iodide. When applied to alk
Tebbe Olefination (Methylenation)
F. N. Tebbe et al., J. Am. Chem. Soc. 100, 3611 (1978); S. H. Pine et al., ibid. 102, 3270 (1980).
Exchange of the oxy
Merrifield Solid-Phase Peptide Synthesis (SPPS)
R. B. Merrifield, J. Am. Chem. Soc. 85, 2149 (1963).
Synthesis of long peptides involving the following
Menschutkin Reaction
N. Menschutkin, Z. Physik. Chem. 5, 589 (1890); 6, 41 (1890).
Reaction of tertiary amines with alkyl halides to form quaternary sal
Meisenheimer Rearrangements
J. Meisenheimer, Ber. 52, 1667 (1919).
Formation of O, N, N-trisubstituted hydroxylamines from tertiary amine oxides via [1,
Meerwein Arylation
H. Meerwein et al., J. Prakt. Chem. 152, 237 (1939).
Formation of arylated olefins on treatment of olefins with diazonium salts in th
Wagner-Meerwein Rearrangement
G. Wagner, J. Russ. Phys. Chem. Soc. 31, 690 (1899); H. Meerwein, Ann. 405, 129 (1914).
-to-carbon migration of alkyl, ary
McMurry Coupling Reaction
J. E. McMurry, M. P. Fleming, J. Am. Chem. Soc. 96, 4708 (1974); S. Tyrlik, I. Wolochowicz, Bull. Soc. Chim. France 1973, 2147; T. Mukaiyama et a
McLafferty Rearrangement
F. W. McLafferty, Anal. Chem. 31, 82 (1959).
Electron-impact-induced cleavage of carbonyl compounds having a hydrogen in the &g
McFadyen-Stevens Reaction
J. S. McFadyen, T. S. Stevens, J. Chem. Soc. 1936, 584.
Base-catalyzed thermal decomposition of acylbenzenesulfonylhydrazines
Martinet Dioxindole Synthesis
A. Guyot, J. Martinet, Compt. Rend. 156, 1625 (1913).
Formation of derivatives of dioxindole from esters of mesoxalic acid
Marschalk Reaction
C. Marschalk et al., Bull. Soc. Chim. France 3, 1545 (1936).
dithionite reduction of 1-hydroxy- or aminoanthraquinones to their leuc
Mannich Reaction
C. Mannich, W. Krosche, Arch. Pharm. 250, 647 (1912).
Reaction of compounds having an active hydrogen with non-enolizable aldehydes and
Malonic Ester Syntheses
Syntheses based on the strongly activated methylene group of malonic esters which on reaction with sodium ethoxide form a resonance-stabilized ion
Madelung Synthesis
W. Madelung, Ber. 45, 1128 (1912).
Formation of derivatives by intramolecular cyclization of an N-(2-alkylphenyl)alkanamide by a str
Lossen Rearrangement
W. Lossen, Ann. 161, 347 (1872); 175, 271, 313 (1874).
Conversion of a hydroxamic acid to an isocyanate via the intermediacy of its
Lobry de Bruyn-van Ekenstein Transformation
C. A. Lobry de Bruyn, Rec. Trav. Chim. 14, 150 (1895); C. A. Lobry de Bruyn, W. A. van Ekenstein, ibid. 195, 203; 16, 262 (1897
