Chiral Cu(II)‐N 4 Complex Catalyzed Asymmetric Aza‐Henry Reaction and Its Application in the Synthesis of β ‐Diamine
Tusharkumar Menapara, Raj Kumar Tak, Eswaran Chinnaraja, Rukhsana I. Kureshy, Parth Patel, Noor‐ul H. Khan
Abstract
Tusharkumar Menapara, Raj Kumar Tak, Eswaran Chinnaraja, Rukhsana I. Kureshy, Parth Patel, Noor‐ul H. Khan
Abstract
Abstract Chiral Cu(II)‐L 3 complex was generated In situ to catalyze the asymmetric aza‐Henry reaction of various isatin derived N ‐Boc ketimines with nitromethane, nitroethane and 1‐nitropropane as nucleophiles at room temperature. High yield (up to 84 %) and excellent chiral induction (ee, up to 99 %) of β ‐nitroamine was obtained in 13 h. The β ‐nitroamine (1 g) was conveniently hydrogenated to enantiomerically pure ( S )‐ β ‐diamine in good yield and high enantioselectivity. The kinetic investigation was undertaken to understand the reaction mechanism of the catalytic aza‐Henry reaction using Cu(II)‐L 3 as catalyst, with nitromethane and isatin N ‐Boc ketimine (1 g) as a representative substrate.
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Abstract Chiral Cu(II)‐L 3 complex was generated In situ to catalyze the asymmetric aza‐Henry reaction of various isatin derived N ‐Boc ketimines with nitromethane, nitroethane and 1‐nitropropane as nucleophiles at room temperature. High yield (up to 84 %) and excellent chiral induction (ee, up to 99 %) of β ‐nitroamine was obtained in 13 h. The β ‐nitroamine (1 g) was conveniently hydrogenated to enantiomerically pure ( S )‐ β ‐diamine in good yield and high enantioselectivity. The kinetic investigation was undertaken to understand the reaction mechanism of the catalytic aza‐Henry reaction using Cu(II)‐L 3 as catalyst, with nitromethane and isatin N ‐Boc ketimine (1 g) as a representative substrate.
Key concepts: Nitromethane, Nitroaldol reaction, Nitroethane, Catalysis, Chemistry, Yield (engineering), Isatin, Nucleophile