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ChemInform Abstract: Asymmetric Synthesis of Chiral Amines via Nucleophilic Addition to Ferrocenylalkyl Substituted Imines.

Dorothy M. David, Leon A. P. Kane‐Maguire, Stephen G. Pyne

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Abstract

Abstract The isomerically pure imine (III) undergoes nucleophilic attack to give the diastereomeric compounds (V) and (VI) from which the amine (VIII) (yield not given) is released and the chiral ferrocenyl auxiliary is regenerated as the acetate (IX).

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What this paper is about

Abstract The isomerically pure imine (III) undergoes nucleophilic attack to give the diastereomeric compounds (V) and (VI) from which the amine (VIII) (yield not given) is released and the chiral ferrocenyl auxiliary is regenerated as the acetate (IX).

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Available abstract

Abstract The isomerically pure imine (III) undergoes nucleophilic attack to give the diastereomeric compounds (V) and (VI) from which the amine (VIII) (yield not given) is released and the chiral ferrocenyl auxiliary is regenerated as the acetate (IX).

Key concepts: Chemistry, Diastereomer, Imine, Nucleophile, Nucleophilic addition, Yield (engineering), Amine gas treating, Chiral auxiliary

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ChemInform Abstract: Asymmetric Synthesis of Chiral Amines via Nucleophilic Addition to Ferrocenylalkyl Substituted Imines. — Research Paper | ScholarLens