Reduction reactions

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1. 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
2. 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.
3. 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.
4. Controlled-potential electrolytic reduction: 1,1-bis(bromomethyl)cyclopropaneReduction Org. Synth. Coll. Vol. 6, p. 153; Vol. 52, p. 22 · Rifi
5. Directed homogeneous hydrogenation: methyl anti-3-hydroxy-2-methylpentanoateReduction Org. Synth. Coll. Vol. 8, p. 420; Vol. 68, p. 64 · Brown et al.
6. 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
7. Discussion Addendum for: palladium-catalyzed reduction of vinyl trifluoromethanesulfonates to alkenes: cholesta-3,5-dieneReduction Org. Synth. Vol. 88, p. 260 · Cacchi et al.
8. Enone reduction-enolate alkylation sequence: 2-allyl-3-methylcyclohexanoneReduction Org. Synth. Coll. Vol. 6, p. 51; Vol. 56, p. 52 · Caine et al.
9. Homogeneous catalytic hydrogenation: dihydrocarvoneReduction Org. Synth. Coll. Vol. 6, p. 459; Vol. 53, p. 63 · Ireland and Bey
10. Hydrogenation of aromatic nuclei: 1-decalolReduction Org. Synth. Coll. Vol. 6, p. 371; Vol. 51, p. 103 · Meyers et al.
11. Indium/ammonium chloride-mediated selective reduction of aromatic nitro compounds: ethyl 4-aminobenzoateReduction Org. Synth. Vol. 81, p. 188 · Banik et al.
12. 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
13. 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.
14. Modified Clemmensen reduction: cholestaneReduction Org. Synth. Coll. Vol. 6, p. 289; Vol. 53, p. 86 · Yamamura et al.
15. Oxymercuration-reduction: alcohols from olefins: 1-methylcyclohexanolReduction Org. Synth. Coll. Vol. 6, p. 766; Vol. 53, p. 94 · Jerkunica and Traylor
16. Palladium catalyst for partial reduction of acetylenes1Reduction Org. Synth. Coll. Vol. 5, p. 880; Vol. 46, p. 89 · Lindlar and Dubuis
17. 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.
18. Platinum catalyst for reductionsReduction Org. Synth. Coll. Vol. 1, p. 463; Vol. 8, p. 92 · Adams et al.
19. 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.
20. Reduction of carboxylic acids to aldehydes: 6-oxodecanalReduction Org. Synth. Coll. Vol. 8, p. 498; Vol. 66, p. 121 · Fujisawa and Sato
21. Reduction of conjugated alkenes with chromium(II) sulfate: diethyl succinateReduction Org. Synth. Coll. Vol. 5, p. 993; Vol. 49, p. 98 · Zurqiyah and Castro
22. 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
23. Reduction of ketones to hydrocarbons with triethylsilane: m-nitroethylbenzeneReduction Org. Synth. Coll. Vol. 7, p. 393; Vol. 60, p. 108 · Fry et al.
24. Reduction of organic halides. Chlorobenzene to benzeneReduction Org. Synth. Coll. Vol. 5, p. 998; Vol. 47, p. 103 · Bryce-Smith and Wakefield