Cinnamyl acetate hydrogenolysis

Vinylogs of benzylic alcohols, e.g. cinnamyl alcohol, undergo easy saturation of the double bond by catalytic hydrogenation over platinum, rhodium-platinum and palladium oxides [39] or by reduction with lithium aluminum hydride [609]. In the presence of acids, catalytic hydrogenolysis of the allylic hydroxyl takes place, especially over platinum oxide in acetic acid and hydrochloric acid [39]. 

---

See also in sourсe #XX -- [ ]

See also in sourсe #XX -- [ ]

See also in sourсe #XX -- [ ]

---