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2001 reduction, hydrogenation reduction, hydrogenation O 0220 37 - 064 Chemoselective Control of Hydrogenation Among Aromatic Car- bonyl and Benzyl Alcohol Derivatives Using Pd/C(en) Catalyst. Employing a heterogeneous Pd/ethylenediamine complex catalyst possessing less catalytic activity than the commercial Pd-C catalyst, the chemoselective hydrogenation of various aromatic carbonyl compounds to benzyl alcohols is achieved and the complete conversion to the corresponding methylene derivatives is avoided. In addition, this catalyst is used in the chemoselective deacetoxylation reaction at the benzylic position in the presence of a benzyl al- cohol functionality within the molecule. — (HATTORI, KAZUYUKI; SAJIKI, HIRONAO; HIROTA, KOSAKU; Tetrahedron 57 (2001) 23, 4817-4824; Lab. Med. Chem., Gifu Pharm. Univ., Mitahora, Gifu 502, Japan; EN) 1

ChemInform Abstract: Chemoselective Control of Hydrogenation Among Aromatic Carbonyl and Benzyl Alcohol Derivatives Using Pd/C(en) Catalyst

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Page 1: ChemInform Abstract: Chemoselective Control of Hydrogenation Among Aromatic Carbonyl and Benzyl Alcohol Derivatives Using Pd/C(en) Catalyst

2001 reduction, hydrogenation

reduction, hydrogenationO 0220

37 - 064Chemoselective Control of Hydrogenation Among Aromatic Car-bonyl and Benzyl Alcohol Derivatives Using Pd/C(en) Catalyst. —Employing a heterogeneous Pd/ethylenediamine complex catalyst possessingless catalytic activity than the commercial Pd-C catalyst, the chemoselectivehydrogenation of various aromatic carbonyl compounds to benzyl alcoholsis achieved and the complete conversion to the corresponding methylenederivatives is avoided. In addition, this catalyst is used in the chemoselectivedeacetoxylation reaction at the benzylic position in the presence of a benzyl al-cohol functionality within the molecule. — (HATTORI, KAZUYUKI; SAJIKI,HIRONAO; HIROTA, KOSAKU; Tetrahedron 57 (2001) 23, 4817-4824; Lab.Med. Chem., Gifu Pharm. Univ., Mitahora, Gifu 502, Japan; EN)

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