Work

Continuous flow photolysis of aryl azides: Preparation of 3H-azepinones

Year: 2011

Type: article

Abstract: Photolysis of aryl azides to give nitrenes, and their subsequent rearrangement in the presence of water to give 3H-azepinones, is performed in continuous flow in a photoreactor constructed of fluorinated ethylene polymer (FEP) tubing. Fine tuning of the reaction conditions using the flow reactor allowed minimization of secondary photochemical reactions.

Source: Beilstein Journal of Organic Chemistry

DOI: 10.3762/bjoc.7.129

Authors: Farhan R Bou-Hamdan, François Lévesque, Alexander G O'Brien, Peter H Seeberger

Institutions: Max Planck Institute of Colloids and Interfaces, Freie Universität Berlin

Language: English

Topic: Chemical Reactions and Mechanisms

Subfield: Physical and Theoretical Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: diamond

Funders: AstraZeneca, Max-Planck-Gesellschaft

OpenAlex ID: W2160382893