The development of a visible light-mediated Giese-type reaction using arylboronic acids as aryl radical source is described. The synthetic protocol capitalizes on the employment of environmentally benign metal-free catalyst to forge Csp2-Csp3 bonds. Applications of the methodology to the synthesis of aminoesters and the anti-inflammatory drug nabumetone, either in batch or in flow, are also reported.

Use of acridinium-based photocatalyst in the Giese-type coupling of arylboronic acids with electron poor olefins / M. Caldarelli, L. Laze, L. Piazza, G. Caputo, M. De Amici, G. Papeo. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 103:(2022 Aug 03), pp. 153978.1-153978.5. [10.1016/j.tetlet.2022.153978]

Use of acridinium-based photocatalyst in the Giese-type coupling of arylboronic acids with electron poor olefins

M. De Amici
Penultimo
;
2022

Abstract

The development of a visible light-mediated Giese-type reaction using arylboronic acids as aryl radical source is described. The synthetic protocol capitalizes on the employment of environmentally benign metal-free catalyst to forge Csp2-Csp3 bonds. Applications of the methodology to the synthesis of aminoesters and the anti-inflammatory drug nabumetone, either in batch or in flow, are also reported.
Visible light photocatalysis; Boronic acids; Giese reaction; Metal free; Nabumetone;
Settore CHIM/08 - Chimica Farmaceutica
Settore CHIM/06 - Chimica Organica
3-ago-2022
3-lug-2022
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/933006
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