ScholarLens Back to search
2021•Letters in Organic ChemistryRequires access

Direct Synthesis of Aromatic Imine Schiff Bases from β-Phenol Hydroxy Ketone

Chang Liu, Haomin Wu, Feng Feng, Wenyuan Liu, Xueyang Jiang

Open publisher page 0 citations

Abstract

Abstract: A facile methodology has been developed to build carbon nitrogen double bond from ketones promoted by the hydroxyl groups in β-phenol hydroxy ketone. It is noteworthy that the halogenated β-phenol hydroxy ketone can chemoselectively react with the amine to afford halogenated phenol imine. It is suitable for certain natural products and also suitable for water-based heteroamines. The method possesses low toxicity and is widely applicable. This strategy is usually used to obtain moderate to good yields of aromatic amine Schiff base.

About this research paper

What this paper is about

Abstract: A facile methodology has been developed to build carbon nitrogen double bond from ketones promoted by the hydroxyl groups in β-phenol hydroxy ketone. It is noteworthy that the halogenated β-phenol hydroxy ketone can chemoselectively react with the amine to afford halogenated phenol imine. It is suitable for certain natural products and also suitable for water-based heteroamines. The method possesses low toxicity and is widely applicable. This strategy is usually used to obtain moderate to good yields of aromatic amine Schiff base.

Why it matters

A significance statement is not available in the OpenAlex record.

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: A facile methodology has been developed to build carbon nitrogen double bond from ketones promoted by the hydroxyl groups in β-phenol hydroxy ketone. It is noteworthy that the halogenated β-phenol hydroxy ketone can chemoselectively react with the amine to afford halogenated phenol imine. It is suitable for certain natural products and also suitable for water-based heteroamines. The method possesses low toxicity and is widely applicable. This strategy is usually used to obtain moderate to good yields of aromatic amine Schiff base.

Key concepts: Chemistry, Phenol, Ketone, Imine, Schiff base, Amine gas treating, Organic chemistry, Polymer chemistry

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
Direct Synthesis of Aromatic Imine Schiff Bases from β-Phenol Hydroxy Ketone — Research Paper | ScholarLens