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1998 alkylation, arylation, dealkylation, dearylation, C-acylation, olefination alkylation, arylation, dealkylation, dearylation, C-acylation, olefination O 0280 49 - 084 Novel Carbonyl-Dependent Regioselective Allylation via Diethylzinc- Mediated Umpolung of π-Allylpalladium. The allylation of carbonyl compounds with allyl esters such as (I) in the presence of diethylzinc and catalytic Pd(0) is investigated. With benzaldehyde mainly α-allylation products (III) are obtained, whereas acetone and ethyl acetate yield γ-allylation products (VII) and (IX). — (KIMURA, M.; OGAWA, Y.; SHIMIZU, M.; SUEISHI, M.; TANAKA, S.; TAMARU, Y.; Tetrahedron Lett. 39 (1998) 38, 6903-6906; Dep. Appl. Chem., Fac. Eng., Nagasaki Univ., Bunkyo, Nagasaki 852, Japan; EN) 1

ChemInform Abstract: Novel Carbonyl-Dependent Regioselective Allylation via Diethylzinc-Mediated Umpolung of π-Allylpalladium

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1998 alkylation, arylation, dealkylation, dearylation, C-acylation, olefination

alkylation, arylation, dealkylation, dearylation, C-acylation, olefinationO 0280

49 - 084Novel Carbonyl-Dependent Regioselective Allylation via Diethylzinc-Mediated Umpolung of π-Allylpalladium. — The allylation ofcarbonyl compounds with allyl esters such as (I) in the presence of diethylzincand catalytic Pd(0) is investigated. With benzaldehyde mainly α-allylationproducts (III) are obtained, whereas acetone and ethyl acetate yield γ-allylationproducts (VII) and (IX). — (KIMURA, M.; OGAWA, Y.; SHIMIZU, M.;SUEISHI, M.; TANAKA, S.; TAMARU, Y.; Tetrahedron Lett. 39 (1998) 38,6903-6906; Dep. Appl. Chem., Fac. Eng., Nagasaki Univ., Bunkyo, Nagasaki852, Japan; EN)

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