A green and sustainable oxime ether formation method via the visible-light-promoted O–H
functionalization of oximes with diazo esters is described. The reaction occurs under very …

Previously synthesized novel chalcone oxime ethers (COEs) were evaluated for inhibitory
activities against monoamine oxidases (MAOs) and acetylcholinesterase (AChE). Twenty …

The [1, 3]-nitrogen rearrangement reactions of O-aryl ketoximes were promoted by N-
heterocyclic carbene (NHC)-copper catalysts and BF3· OEt2 as an additive, affording ortho …

This study describes an efficient approach to access oxime ethers via P (III)-mediated O–H
bond insertion reaction of oximes with α-keto esters. The strategy involves the protonation of …

A panel of 30 chalcone derivatives, including 19 aldoxime-chalcone ethers (ACE), and 11
hydroxyl‑chalcones (HC), previously synthesized using a Pd-catalyzed C–O cross-coupling …

Main observation and conclusion A facile copper‐based catalytic system has been
developed to enable efficient cyclization of methylketoximes and alkynals. This protocol …

An unprecedented copper-catalyzed oxidative dehydrogenative [3+ 2] annulation of O-acyl
oximes containing α-C (sp3)–H bonds with α-amino ketones for the preparation of 3 …

Oxime ethers are extensively present as key components in numerous active
pharmaceutical ingredients and many other synthetically viable organic compounds. Herein …

A mild and efficient one-pot method has been developed for the synthesis of oxime ether
derivatives with up to 85% yield by employing tert-butyl nitrite (TBN) as nitrogen source …

Abstract A series of 1, 3-diarylprop-2-en-1-one oximes (7-12) were synthesized via reaction
of 1, 3-diarylprop-2-en-1-one (1-6) with NH2OH. HCl in dry pyridine. In order to produce the …