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Synfacts 2010(2): 0185-0185
DOI: 10.1055/s-0029-1219100
DOI: 10.1055/s-0029-1219100
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Hydrogenolysis of Benzylic C-C Bonds Catalyzed by Pd/C
A. Wilsily, Y. Nguyen, E. Fillion*
University of Waterloo, Canada
Further Information
Publication History
Publication Date:
21 January 2010 (online)

Significance
While the hydrogenolysis of C-Z bonds (Z = N, O, S, halogen) is well known, the corresponding reactions of unstrained sp³ C-C bonds have been unexplored. Most reports of C-C bond hydrogenolysis require high temperatures/pressures, substrates with strained rings, or aromatization as the driving force. The authors report that a catalytic amount of Pd/C under hydrogen in methanol readily cleaves benzylic C-C bonds of various Meldrum’s acid derivatives to provide tertiary benzylic compounds in good yields. Unfortunately, substrates containing meta-substitution in the aromatic ring were unreactive.