“…In the case of hydrogenation of carboxylic acids, selectivity/enantioselectivity to alcohols depends to a great extent on conditions of the heterogeneous catalytic reaction, primarily on the number and type of functional groups in the platform molecule. Impressive selectivities to alcohols were reached in recent years upon hydrogenation of fatty acids [1][2][3][4][5][6][7][8] , bifunctional acids having an additional carbonyl (for example, levulinic acid [9,10] ) or hydroxyl group (lactic acid as a typical example [11,12] ), and dibasic carboxylic acids (mostly succinic acid [9,[13][14][15] ). Products of the indicated reactions -mono-and diatomic alcohols -are the key intermediates for the production of lubricants, surfactants, plasticizers, and other specialty chemicals and polymers.…”