Mukaiyama Aldol Reaction
T. Mukaiyama et al., Chem Lett. 1973, 1011; idem et al., ibid. 1974, 323; eidem, J. Am. Chem. Soc. 96, 7503 (1974).
Formation o
Wessely-Moser Rearrangement
F. Wessely, G. H. Moser, Monatsh. 56, 97 (1930).
Rearrangement of flavones and flavanones possessing a 5-hydroxyl group, thr
Moore Myers Cyclization; Moore Cyclization; Myers Cyclization
J. O. Karlsson et al., J. Am. Chem. Soc. 107, 3392 (1985); A. G. Myers et al., ibid. 111, 8057 (1989); R. Nag
Swern Oxidation (Moffatt-Swern Oxidation)
K. Omura, D. Swern, Tetrahedron 34, 1651 (1978).
Mild oxidation of primary and secondary alcohols, promoted by
Pfitzner-Moffatt Oxidation (Moffatt Oxidation)
K. E. Pfitzner, J. G. Moffatt, J. Am. Chem. Soc. 85, 3027 (1963).
Mild oxidation of primary and secondary
Mitsunobu Reaction
O. Mitsunobu et al., Bull. Chem. Soc. Japan 40, 935 (1967); O. Mitsunobu, Y. Yamada, ibid. 2380.
Condensation of alcohols and acidic
Milas Hydroxylation of Olefins
N. A. Milas et al., J. Am. Chem. Soc. 58, 1302 (1936); 59, 543, 2342, 2345 (1937); 61, 1844 (1939); 62, 1841 (1940).
Form
Mignonac Reaction
G. Mignonac, Compt. Rend. 172, 223 (1921).
Formation of amines by catalytic hydrogenation of aldehydes or ketones in liquid ammonia an
Miescher Degradation
C. Meystre et al., Helv. Chim. Acta 27, 1815 (1944).
Adaptation of the Barbier-Wieland degradation, q.v., to permit simultaneous el
Mukaiyama-Michael Reaction
K. Narasaka et al., Bull. Chem. Soc. Japan 49, 779 (1976).
Formation of 1,5-dicarbonyl compounds by reaction of ketene silyl
Meyers Aldehyde Synthesis
A. I. Meyers et al., J. Am. Chem. Soc. 91, 763 (1969); eidem, J. Org. Chem. 38, 36 (1973).
Synthesis of aldehydes from alkylha
Meyer-Schuster Rearrangement; Rupe Rearrangement
K. H. Meyer, K. Schuster, Ber. 55, 819 (1922); H. Rupe, E. Kambli, Helv. Chim. Acta 9, 672 (1926).
Acid
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
