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- W1983669046 endingPage "126" @default.
- W1983669046 startingPage "81" @default.
- W1983669046 abstract "Abstract The synthesis of a large number of fine chemicals, particularly in the field of flavor and fragrance chemistry [1,2] and pharmaceuticals [3], involves the selective hydrogenation of unsaturated carbonyl intermediates as a critical step. The hydrogenation of α,β-unsaturated carbonyls into saturated carbonyls is comparatively easy to achieve because thermodynamics favor the hydro-genation of the C═C bonds; therefore, research efforts were more directed at improving the selectivity to unsaturated alcohols. When a substituent is present on the carbon atom of the carbonyl group (i.e. with ketones), there is no chance to hydrogenate selectively the C═O bond, and saturated ketones are obtained with a high yield. This review is thus mostly restricted to the hydrogenation of α, β-unsaturated aldehydes into the corresponding unsaturated alcohols." @default.
- W1983669046 created "2016-06-24" @default.
- W1983669046 creator A5062576325 @default.
- W1983669046 creator A5074169256 @default.
- W1983669046 date "1998-02-01" @default.
- W1983669046 modified "2023-10-17" @default.
- W1983669046 title "Selective Hydrogenation of α,β-Unsaturated Aldehydes" @default.
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