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  1. Oxymercuration-reduction: alcohols from olefins: 1-methylcyclohexanolReduction Org. Synth. Coll. Vol. 6, p. 766; Vol. 53, p. 94 · Jerkunica and Traylor
  2. Palladium catalyst for partial reduction of acetylenes1Reduction Org. Synth. Coll. Vol. 5, p. 880; Vol. 46, p. 89 · Lindlar and Dubuis
  3. Palladium-catalyzed reduction of vinyl trifluoromethanesulfonates to alkenes: cholesta-3,5-dieneReduction Org. Synth. Coll. Vol. 8, p. 126; Vol. 68, p. 138 · Cacchi et al.
  4. Platinum catalyst for reductionsReduction Org. Synth. Coll. Vol. 1, p. 463; Vol. 8, p. 92 · Adams et al.
  5. Reduction of alkyl halides and tosylates with sodium cyanoborohydride in hexamethylphosphoric triamide (HMPA):A. 1-Iododecane to n-decaneb. 1-Dodecyl tosylate to n-dodecaneReduction Org. Synth. Coll. Vol. 6, p. 376; Vol. 53, p. 107 · Hutchins et al.
  6. Reduction of carboxylic acids to aldehydes: 6-oxodecanalReduction Org. Synth. Coll. Vol. 8, p. 498; Vol. 66, p. 121 · Fujisawa and Sato
  7. Reduction of conjugated alkenes with chromium(II) sulfate: diethyl succinateReduction Org. Synth. Coll. Vol. 5, p. 993; Vol. 49, p. 98 · Zurqiyah and Castro
  8. Reduction of ketones by use of the tosylhydrazone derivatives: androstan-17 β-olReduction Org. Synth. Coll. Vol. 6, p. 62; Vol. 52, p. 122 · Caglioti
  9. Reduction of ketones to hydrocarbons with triethylsilane: m-nitroethylbenzeneReduction Org. Synth. Coll. Vol. 7, p. 393; Vol. 60, p. 108 · Fry et al.
  10. Reduction of organic halides. Chlorobenzene to benzeneReduction Org. Synth. Coll. Vol. 5, p. 998; Vol. 47, p. 103 · Bryce-Smith and Wakefield
  11. Reduction of quinones with hydriodic acid: benz[a]anthraceneReduction Org. Synth. Coll. Vol. 7, p. 18; Vol. 62, p. 165 · Konieczny and Harvey
  12. Reduction of sulfonyl halides with zinc powder: S-methyl methanethiosulfonateReduction Org. Synth. Vol. 78, p. 99 · Chemla and Karoyan
  13. Reduction of α-amino acids: L-valinolReduction Org. Synth. Coll. Vol. 7, p. 530; Vol. 63, p. 136 · Dickman et al.
  14. Removal of Nα-benzyloxycarbonyl groups from sulfur-containing peptides by catalytic hydrogenation in liquid ammonia: O-tert-butyl-L-seryl-S-tert-butyl-L-cysteine tert-butyl esterReduction Org. Synth. Coll. Vol. 6, p. 252; Vol. 59, p. 159 · Felix et al.
  15. Stereospecific reduction of propargyl alcohols: (E)-3-trimethylsilyl-2-propen-1-olReduction Org. Synth. Coll. Vol. 7, p. 524; Vol. 64, p. 182 · Jones and Denmark
  16. Synthesis and ru(II)-BINAP reduction of a ketoester derived from hydroxyproline: 2(S)-(β-tert-butoxycarbonyl-α-(S) and α-(R)-hydroxyethyl)-4(R)-hydroxypyrrolidine-1-carboxylic acid, tert-butyl esterReduction Org. Synth. Vol. 81, p. 178 · King et al.
  17. Synthesis of 4-triisopropylsilyl-3-butyn-2-ol by asymmetric transfer hydrogenationReduction Org. Synth. Vol. 84, p. 120 · Marshall et al.
  18. Synthesis of Highly Enantiomerically Enriched Amines by Asymmetric Transfer Hydrogenation of N-(tert-Butylsulfinyl)IminesReduction Org. Synth. Vol. 90, p. 338 · Guijarro et al.
  19. Yeast reduction of 2,2-dimethylcyclohexane-1,3-dione: (S)-(+)-3-hydroxy-2,2-dimethylcyclohexanone)Reduction Org. Synth. Coll. Vol. 8, p. 312; Vol. 68, p. 56 · Mori and Mori
  20. Yeast reduction of ethyl acetoacetate: (S)-(+)-ethyl 3-hydroxybutanoateReduction Org. Synth. Coll. Vol. 7, p. 215; Vol. 63, p. 1 · Seebach et al.