- Meerwein-Ponndorf-Verley Reduction
-
Meerwein-Ponndorf-Verley Reduction ( Alkoxide Reduction)
H. Meerwein, R. Schmidt, Ann. 444, 221 (1925); W. Ponndorf, Angew. Chem. 39, 138 (1926); A. Verley, Bull. Soc. Chim. France 37, 537, 871 (1925).
Reduction of aldehydes or ketones to the corresponding alcohols with aluminum alkoxides (the reverse of the Oppenauer oxidation, q.v.):

Reviews: A. L. Wilds, Org. React. 2, 178-202 (1944); R. M. Kellogg, Comp. Org. Syn. 8, 88-91 (1991); C. F. de Graauw et al., Synthesis 10, 1007-1017 (1994). Enantioselectivity: D. A. Evans et al., J. Am. Chem. Soc. 115, 9800 (1993); M. Node et al., ibid. 122, 1927 (2000). Modified conditions: P. S. Kumbhar et al., Chem. Commun., 1998, 535; T. Ooi et al., J. Am. Chem. Soc. 120, 10790 (1998); Y. Nakano et al., Tetrahedron Letters 41, 1565 (2000). Cf. Cannizzaro Reaction; Tischenko Reaction.
Prev: Amadori Rearrangement
Next: Allylic Rearrangements - 【Back】【Close 】【Print】【Add to favorite 】
-
Health and Chemical more >
-
Hot Products
- 7758-98-7 Sulfuric acidcopper(2+) salt (1:1)
- 87901-60-8 4,4'-BIS(TRIFLUOROMETHYL)DIPHENYLMETHANE
- 1227096-09-4 D Glucose
- 842123-94-8 2-(1,3-Dioxolan-2-ylmethyl)-1-fluorobenzene
- 9086-52-6 Poly(oxy-1,2-ethanediyl), .alpha.-bis(1-phenylethyl)phenyl-.omega.-hydroxy-
- 484-12-8 Osthole
- 105-56-6 Ethyl cyanoacetate
- 66563-30-2 (1S,10aS)-3β-(3-Furyl)-1,3,4,5,6,11,12,12aα-octahydro-1,4aβ-(epoxymethano)-4aH-furo[3',4':4a,5]naphtho[2,1-c]pyran-8(4bαH)-one
- 122-80-5 Acetamide,N-(4-aminophenyl)-
- 22246-18-0 3,4-Dihydro-7-hydroxy-2(1H)-quinolinone
- 61788-37-2 Hexanoic acid, 2-ethyl-, rare earth salts
- 832-09-7 CIS-1,3-DIACETOXYCYCLOHEXANE


