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

Sani Monica
Primo
;
Volonterio Alessandro
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.
2022
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
multicomponent reactions
domino process
amphiphilic molecules
cationic lipids
antibacterial
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/417799
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