Rediscovering aminal chemistry: copper(ii) catalysed formation under mild conditions. Issue 21 (14th October 2020)

• Record Type: Journal Article
• Authors: Pereira, Juliana G.; António, João P. M.; Mendonça, Ricardo; Gomes, Rafael F. A.; Afonso, Carlos A. M.
• Is Part Of: Green chemistry. Volume 22:Issue 21(2020)
• Page Start: 7484
• Page End: 7490
• Publication Date: 2020-10-14
• Subjects: Environmental chemistry -- Industrial applications -- Periodicals; Environmental management -- Periodicals; 660
• DOI: 10.1039/d0gc01977a
• Languages: English
• ISSNs: 1463-9262

Abstract

Abstract : Aminals are an interesting moiety limited by the harsh conditions preceding their preparation. Herein is described a novel procedure for the preparation of aminals under mild conditions and explore their stability and applications. Abstract : Aminals, the N, N analogues of acetals, have been thoroughly explored in organic chemistry, with a particular focus on heteroaromatic aldehyde lithiation. Nevertheless, the existing methodologies for their formation typically employ harsh conditions limiting their usefulness. In this work, we present an efficient and mild methodology for the preparation of aminals from aromatic aldehydes, including furanic platforms. These mild conditions allowed ease of access to a plethora of aminals and as such we set out to explore previously unaccessible potential applications. By studying the stability of various aminals, we were able to develop a simple aldehyde protecting group based on a commercial diamine which is deprotected under mind conditions. We developed a protocol for the scavenging of genotoxic aldehydes by taking advantage of our methodology and a diamine resin, as well as early studies on the development of a stimuli-responsive release system using a salycil aldehyde derived aminal.