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• W1972689596 abstract "Catalyst-controlled asymmetric ring opening of a racemic oxabicyclic alkene leads to two readily separable regioisomeric products both in excellent ee. A cationic Rh catalyst, with added NH(4)BF(4) to modulate reactivity, was required to obtain synthetically useful yields. The utility of each substituted aminotetralin product has been demonstrated by their conversion to different biologically relevant molecules in a highly efficient and practical manner." @default.
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• W1972689596 date "2010-11-02" @default.
• W1972689596 modified "2023-09-30" @default.
• W1972689596 title "Practical Asymmetric Synthesis of Bioactive Aminotetralins from a Racemic Precursor Using a Regiodivergent Resolution" @default.
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• W1972689596 doi "https://doi.org/10.1021/ol1022239" @default.
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