Na/Hg
Nitrostyrene reduced to amphetamine
G.A. Alles, Salts of 1-phenyl-2-aminopropane.
Patent US1879003
Sept. 1932. C.A. 27: 373 (1933).
LiAlH4
Nitrostyrene reduced to amphetamine
R.T. Gilsdorf and F.F. Nord, Reverse addition of lithium aluminum hydride to nitroolefins.
J. Am. Chem. Soc., 74 (1952) 1837-1843.
Post 443723
(GC_MS: "Reverse Addition of LAH to Nitroölefins - A", Novel Discourse)Raney Nickel (Ni-Al)
Nitrostyrene reduced to amphetamine
J.B. Tindall, Reduction of nitro olefins.
Patent US2636901
Apr. 28, 1953. C.A. 48: 2771f (1954).
Nitrostyrene reduced to amphetamine
G. Stochdorph and O. Schickh, Saturated amines.
Patent DE848197
, Sept. 1, 1952. C.A. 47: 5438b (1953).
Urushibara Ni
https://www.thevespiary.org/rhodium/Rhodium/chemistry/amph.urushibara.txt
Red-Al
https://www.thevespiary.org/rhodium/Rhodium/chemistry/red-al.html
Al/Hg
https://www.thevespiary.org/rhodium/Rhodium/chemistry/znhg.alhg.reductions.txt
diisobutylaluminum hydride (DIBAH)- should work
https://www.thevespiary.org/rhodium/Rhodium/chemistry/phenethylamines.dibah.html
ZnBH4
https://www.thevespiary.org/rhodium/Rhodium/archive/zinc.borohydride.pdf
Nickel Boride/N2H2
https://www.thevespiary.org/rhodium/Rhodium/chemistry/it-290.html
Platinum on Carbon
Bacteria
Reduction of nitroolefin using microorganisms.
Chemical and Pharmaceutical Bulletin 38(12), 3449-51 (1990)
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