Transfer hydrogenation is a chemical reaction in which hydrogen is transferred from one molecule to another. It is often used for the reduction of unsaturated organic compounds (e.g., double bonds or carbonyl groups) by using a hydrogen donor, typically a metal catalyst. This process is significant in various industrial and laboratory applications.
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[Ru(η6-Ph(CH2)3-ethylenediamine-N-toluenesulfonyl)Cl]
N-(2-allylcyclohexylidene)(phenyl)methanamine
C78H102N6O12
1-isopropyl-4-methyl-1,2,3,4-tetrahydroquinoline
Benzene, 1-fluoro-4-(nitromethyl)-
(1S,3R,4R)-3-(toluene-4-sulfonyloxymethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester
(S)-4-methoxy-N-(1-p-tolylpropyl)aniline
Phosphorinane, 3-methyl-1-phenyl-, 1-oxide
propan-2-yl 3-(propan-2-yloxy)propanoate
(E)-2-(4-chloro-phenylmethylene)-cyclohexanol
1-(2-thienyl)-N-tosylethanimine
C13H15N2O(1+)*Br(1-)
N-butyl-5-methyl-2-pyrrolidinone
Quinoline, 1,2-dihydro-2,2,4-trimethyl-7-(phenylmethoxy)-
