2017ChemistrySelectRequires access

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

Open publisher page 6 citations

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.

About this research paper

What this paper is about

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.

Why it matters

OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Nitromethane, Nitroaldol reaction, Nitroethane, Catalysis, Chemistry, Yield (engineering), Isatin, Nucleophile

Related papers

Back to paper searchBrowse research topicsOriginal source
Chiral Cu(II)‐N 4 Complex Catalyzed Asymmetric Aza‐Henry Reaction and Its Application in the Synthesis of β ‐Diamine — Research Paper | ScholarLens