RESEARCHES ON ALDEHYDES. IV. THE CATALYTIC REDUCTION OF SIMPLE AND OF SUBSTITUTED CINNAMIC ALDEHYDES
MT Bogert, G Powell
Index: Bogert; Powell Journal of the American Chemical Society, 1931 , vol. 53, p. 2747,2752
Full Text: HTML
Citation Number: 7
Abstract
,( ArCH=CRCH3 ArCHzCRHCH20H ) + HZ - ArCHzCRHCH3 In our experiments we followed the process of Skita,4 using colloidal palladium as the catalyst in most cases, since he found that with cinnamic aldehyde itself this process caused neither hydrogenation of the benzene nucleus nor formation of bimolecular compounds, under conditions similar to ours. With one mole of hydrogen per mole of cinnamic aldehyde, he reported that his product was nearly ...
Related Articles:
[Marchetti, Mauro; Minello, Fabiola; Paganelli, Stefano; Piccolo, Oreste Applied Catalysis A: General, 2010 , vol. 373, # 1-2 p. 76 - 80]
[Di Dio, Sabrina; Marchetti, Mauro; Paganelli, Stefano; Piccolo, Oreste Applied Catalysis A: General, 2011 , vol. 399, # 1-2 p. 205 - 210]
A new synthesis of aryl??aliphatic alcohols. IV. Application of the method to bicyclic hydrocarbons
[Drukker; Beets Recueil des Travaux Chimiques des Pays-Bas, 1951 , vol. 70, p. 29,33]
A new synthesis of aryl??aliphatic alcohols. IV. Application of the method to bicyclic hydrocarbons
[Drukker; Beets Recueil des Travaux Chimiques des Pays-Bas, 1951 , vol. 70, p. 29,33]