Issue 2, 2024, Issue in Progress

Photocatalytic intermolecular bromonitroalkylation of styrenes: synthesis of cyclopropylamine derivatives and their evaluation as LSD1 inhibitors

Abstract

A mild and efficient method for photoredox-catalyzed bromonitroalkylation of alkenes is described herein. In this reaction, bromonitromethane serves as a source of both nitroalkyl and bromine for direct and regioselective formation of C–Br and C–C bonds from alkenes, and additional cyclization provides C–C bonds to the cyclopropylamine core as an LSD1 inhibitor.

Graphical abstract: Photocatalytic intermolecular bromonitroalkylation of styrenes: synthesis of cyclopropylamine derivatives and their evaluation as LSD1 inhibitors

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2023
Accepted
16 Dec 2023
First published
02 Jan 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 831-835

Photocatalytic intermolecular bromonitroalkylation of styrenes: synthesis of cyclopropylamine derivatives and their evaluation as LSD1 inhibitors

D. Kim, H. Jeon, Y. Kwak, S. J. Lee, T. Nam, J. H. Yu, H. An and K. B. Hong, RSC Adv., 2024, 14, 831 DOI: 10.1039/D3RA07830B

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