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• W2953128918 abstract "The palladium-induced cleavage at room temperature of (2-methyl-1-tetralenyl) benzyl carbonate under bubbling of hydrogen led to (R) 2-methyltetral-1-one with 90% chemical yield and 64% enantiomeric excess in the presence of catalytic amounts of (+) endo-2-hydroxy-endo-3-aminobornane." @default.
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• W2953128918 date "1995-08-01" @default.
• W2953128918 modified "2023-09-25" @default.
• W2953128918 title "Palladium-mediated enantioselective formation of 2-methyltetral-1-one from the corresponding allyl or benzyl enol carbonate in the presence of enantiopure aminoalcohols" @default.
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• W2953128918 doi "https://doi.org/10.1016/0957-4166(95)00238-k" @default.
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