Palladium-catalyzed oxidative amination of homoallylic alcohols: sequentially installing carbonyl and amino groups along an alkyl chain. Issue 75 (7th September 2017)

• Record Type: Journal Article
• Authors: Ouyang, Lu; Huang, Jiuzhong; Li, Jianxiao; Qi, Chaorong; Wu, Wanqing; Jiang, Huanfeng
• Is Part Of: Chemical communications. Volume 53:Issue 75(2017)
• Page Start: 10422
• Page End: 10425
• Publication Date: 2017-09-07
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c7cc06077g
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : A novel Pd-catalyzed intermolecular oxidative amination of homoallylic alcohols affording valuable β-amino acetones under mild conditions has been developed. Abstract : A novel Pd-catalyzed intermolecular cascade oxidative amination of homoallylic alcohols to yield β-amino ketones has been developed by using TBHP as the terminal oxidant. The synthetic utility of the reaction can be performed by installing the carbonyl and amino groups along an alkyl chain in one step, offering several advantages such as simple starting materials and easy operation. The resultant β-amino ketones should have potential applications in the fields of biopharmaceutical and functional materials.