chempirical
Reaction database

Reduction reactions

3,374 reactions: 10 worked examples with a reagent table you can scale, 503 named reactions and 2,861 checked procedures from Organic Syntheses.

1–24 of 44

  1. N-Acetyl-N-phenylhydroxylamine via catalytic transfer hydrogenation of nitrobenzene using hydrazine and rhodium on carbonReduction Org. Synth. Coll. Vol. 8, p. 16; Vol. 67, p. 187 · Oxley et al.
  2. Acetylenic ethers from alcohols and their reduction to Z- and E-enol ethers: preparation of 1-menthoxy-1-butyne from menthol and conversion to (Z)- and (E)-1-menthoxy-1-buteneReduction Org. Synth. Coll. Vol. 9, p. 533; Vol. 74, p. 13 · Kann et al.
  3. Aldehydes from acid chlorides by modified Rosenmund reduction: 3,4,5-trimethoxybenzaldehydeReduction Org. Synth. Coll. Vol. 6, p. 1007; Vol. 51, p. 8 · Rachlin et al.
  4. Aldehydes from acid chlorides by reduction of ester-mesylates with sodium borohydride: cyclobutanecarboxaldehydeReduction Org. Synth. Coll. Vol. 6, p. 312; Vol. 51, p. 11 · Johnson and Rickborn
  5. Alkylation of the anion from Birch reduction of o-anisic acid: 2-heptyl-2-cyclohexenoneReduction Org. Synth. Coll. Vol. 7, p. 249; Vol. 61, p. 59 · Taber et al.
  6. Apparatus for catalytic reductionReduction Org. Synth. Coll. Vol. 1, p. 61; Vol. 8, p. 10 · Adams and Voorhees
  7. Asymmetric hydrogenation of 3-oxo carboxylates using BINAP-ruthenium complexes: (R)-(−)-methyl 3-hydroxybutanoateReduction Org. Synth. Coll. Vol. 9, p. 589; Vol. 71, p. 1 · Kitamura et al.
  8. Asymmetric hydrogenation of allylic alcohols using BINAP-ruthenium complexes: (S)-(−)-citronellolReduction Org. Synth. Coll. Vol. 9, p. 169; Vol. 72, p. 74 · Takaya et al.
  9. Asymmetric hydrogenation of ketopantoyl lactone: D-(−)-pantoyl lactoneReduction Org. Synth. Coll. Vol. 7, p. 417; Vol. 63, p. 18 · Ojima et al.
  10. Asymmetric reduction of α,β-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane: (R)-(+)-1-octyn-3-olReduction Org. Synth. Coll. Vol. 7, p. 402; Vol. 63, p. 57 · Midland and Graham
  11. Catalytic enantioselective borane reduction of benzyl oximes: preparation of (S)-1-pyridin-3-yl-ethylamine bis hydrochlorideReduction Org. Synth. Vol. 87, p. 36 · Huang and Ortiz-Marciales
  12. Catalytic reduction of amides to amines with hydrosilanes using a triruthenium carbonyl cluster as the catalystReduction Org. Synth. Vol. 82, p. 188 · Motoyama et al.
  13. Conjugate reduction of α,β-unsaturated p-toluenesulfonylhydrazones to alkenes with catecholborane: 5β-cholest-3-eneReduction Org. Synth. Coll. Vol. 6, p. 293; Vol. 59, p. 42 · Kabalka et al.
  14. Controlled-potential electrolytic reduction: 1,1-bis(bromomethyl)cyclopropaneReduction Org. Synth. Coll. Vol. 6, p. 153; Vol. 52, p. 22 · Rifi
  15. Directed homogeneous hydrogenation: methyl anti-3-hydroxy-2-methylpentanoateReduction Org. Synth. Coll. Vol. 8, p. 420; Vol. 68, p. 64 · Brown et al.
  16. erythro-Directed reduction of a β-keto amide: erythro-1-(3-hydroxy-2-methyl-3-phenylpropanoyl)piperidineReduction Org. Synth. Coll. Vol. 8, p. 326; Vol. 69, p. 44 · Fujita and Hiyama
  17. Discussion Addendum for: palladium-catalyzed reduction of vinyl trifluoromethanesulfonates to alkenes: cholesta-3,5-dieneReduction Org. Synth. Vol. 88, p. 260 · Cacchi et al.
  18. Enone reduction-enolate alkylation sequence: 2-allyl-3-methylcyclohexanoneReduction Org. Synth. Coll. Vol. 6, p. 51; Vol. 56, p. 52 · Caine et al.
  19. Homogeneous catalytic hydrogenation: dihydrocarvoneReduction Org. Synth. Coll. Vol. 6, p. 459; Vol. 53, p. 63 · Ireland and Bey
  20. Hydrogenation of aromatic nuclei: 1-decalolReduction Org. Synth. Coll. Vol. 6, p. 371; Vol. 51, p. 103 · Meyers et al.
  21. Indium/ammonium chloride-mediated selective reduction of aromatic nitro compounds: ethyl 4-aminobenzoateReduction Org. Synth. Vol. 81, p. 188 · Banik et al.
  22. Indoles from 2-methylnitrobenzenes by condensation with formamide acetals followed by reduction: 4-benzyloxyindoleReduction Org. Synth. Coll. Vol. 7, p. 34; Vol. 63, p. 214 · Batcho and Leimgruber
  23. Methyl groups by reduction of aromatic carboxylic acids with trichlorosilane - tri-n-propylamine: 2-methylbiphenylReduction Org. Synth. Coll. Vol. 6, p. 747; Vol. 56, p. 83 · Li et al.
  24. Modified Clemmensen reduction: cholestaneReduction Org. Synth. Coll. Vol. 6, p. 289; Vol. 53, p. 86 · Yamamura et al.