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- W2015325966 abstract "Key steps of the synthesis of optically active aminotetralins (VI) are the regioselective ring opening of aziridine (II) (or its Cbz analogue) with in situ generated arylcuprate reagents as well as Friedel—Crafts cyclization of the free acids (IV) (not optimized)." @default.
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- W2015325966 date "2011-02-17" @default.
- W2015325966 modified "2023-09-26" @default.
- W2015325966 title "ChemInform Abstract: Synthesis of Substituted (S)-2-Aminotetralins via Ring-Opening of Aziridines Prepared from L-Aspartic Acid β-tert-Butyl Ester." @default.
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- W2015325966 doi "https://doi.org/10.1002/chin.201111106" @default.
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