Over the last years, photoredox catalysis has spread as an essential tool to generate radicals under mild and selective conditions and it was applied for the synthesis of heterocyclic structures via cascade cyclizations (10.1021/acs.chemrev.0c00030). Considering this background and the interest of our group in the synthesis of polycyclic indoles, we developed a synthesis of indole-fused 1,4-diazepinones through a cascade radical addition on the C–C double bond of N-indolyl phenylacrylamides, followed by cyclization at indole C2-position (10.1002/adsc.202300708).

Synthesis of indole-fused 1,4-diazepinones through photocatalytic strategies / S. Meraviglia, V. Pirovano, E. Brambilla, G. Abbiati. ((Intervento presentato al 37. convegno New Trends in Organic Synthesis : November, 27th tenutosi a Milan nel 2023.

Synthesis of indole-fused 1,4-diazepinones through photocatalytic strategies

S. Meraviglia
;
V. Pirovano
;
2023

Abstract

Over the last years, photoredox catalysis has spread as an essential tool to generate radicals under mild and selective conditions and it was applied for the synthesis of heterocyclic structures via cascade cyclizations (10.1021/acs.chemrev.0c00030). Considering this background and the interest of our group in the synthesis of polycyclic indoles, we developed a synthesis of indole-fused 1,4-diazepinones through a cascade radical addition on the C–C double bond of N-indolyl phenylacrylamides, followed by cyclization at indole C2-position (10.1002/adsc.202300708).
27-nov-2023
Nitrogen heterocycles; Homogeneous catalysis; Synthetic methods; Radical reactions; Cyclization;
Settore CHIM/06 - Chimica Organica
Società Chimica Italiana (SCI)
Sezione Lombardia Società Chimica Italiana (SCI)
http://www.sintesi.unimi.it/
Synthesis of indole-fused 1,4-diazepinones through photocatalytic strategies / S. Meraviglia, V. Pirovano, E. Brambilla, G. Abbiati. ((Intervento presentato al 37. convegno New Trends in Organic Synthesis : November, 27th tenutosi a Milan nel 2023.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1041763
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