An efficient multicomponent sequential process, which occurs in mild condition has been exploited for the synthesis of systematically modified amphiphilic molecules where the cationic head is tethered to a lipophilic tail through a dihydroorotic acid linker. The process is operatively simple, high yielding, and flexible. Such a strategy could impact combinatorial synthesis of wide libraries of amphiphilic molecules to be tested as transfection agents and/or as antimicrobials.

Multi-Component Sequential Synthesis of Dihydroorotic Acid-Based Amphiphilic Molecules / M. Sani, M.C. Bellucci, A. Volonterio. - In: SYNTHESIS. - ISSN 1764-6103. - 54:23(2022 Dec), pp. 5311-5323. [10.1055/a-1913-3105]

Multi-Component Sequential Synthesis of Dihydroorotic Acid-Based Amphiphilic Molecules

M.C. Bellucci
Secondo
;
2022

Abstract

An efficient multicomponent sequential process, which occurs in mild condition has been exploited for the synthesis of systematically modified amphiphilic molecules where the cationic head is tethered to a lipophilic tail through a dihydroorotic acid linker. The process is operatively simple, high yielding, and flexible. Such a strategy could impact combinatorial synthesis of wide libraries of amphiphilic molecules to be tested as transfection agents and/or as antimicrobials.
multicomponent reactions; domino process; amphiphilic molecules; cationic lipids; antibacterial;
Settore CHIM/06 - Chimica Organica
dic-2022
ago-2022
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1020226
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