TY - JOUR
T1 - Biomass derived Cu2O nanoparticles for N-atom insertion reactions
T2 - a base-free synthesis of quinazolinones with a green approach
AU - Thrilokraj, R.
AU - Małecki, Jan Grzegorz
AU - Budagumpi, Srinivasa
AU - Kshirsagar, Umesh A.
AU - Dateer, Ramesh B.
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/3/6
Y1 - 2024/3/6
N2 - The present study describes the use of a novel and eco-friendly biogenic approach for the synthesis of copper oxide nanoparticles (Cu2O NPs) utilizing Cucumis melo (musk melon) peel extract for the first time. The extract was discovered to consist of active chemical constituents that function as both reducing and stabilizing agents. The successful synthesis of Cu2O NPs is authenticated by several analytical and spectroscopic characterization methods. Furthermore, the catalytic performance of Cu2O NPs was examined for a cost-effective, sustainable and base-free synthesis of pharmaceutically important quinazolinone derivatives without the use of external ligands or additives. Significantly, the molecular complexation of the synthesized N-heterocycles is being examined, and successful synthesis of targets on a gram scale has been accomplished. Furthermore, the recyclability of the catalyst, control experiments, and the clarification of the underlying mechanisms were discussed in detail.
AB - The present study describes the use of a novel and eco-friendly biogenic approach for the synthesis of copper oxide nanoparticles (Cu2O NPs) utilizing Cucumis melo (musk melon) peel extract for the first time. The extract was discovered to consist of active chemical constituents that function as both reducing and stabilizing agents. The successful synthesis of Cu2O NPs is authenticated by several analytical and spectroscopic characterization methods. Furthermore, the catalytic performance of Cu2O NPs was examined for a cost-effective, sustainable and base-free synthesis of pharmaceutically important quinazolinone derivatives without the use of external ligands or additives. Significantly, the molecular complexation of the synthesized N-heterocycles is being examined, and successful synthesis of targets on a gram scale has been accomplished. Furthermore, the recyclability of the catalyst, control experiments, and the clarification of the underlying mechanisms were discussed in detail.
UR - http://www.scopus.com/inward/record.url?scp=85187986068&partnerID=8YFLogxK
U2 - 10.1039/d4gc00569d
DO - 10.1039/d4gc00569d
M3 - Article
AN - SCOPUS:85187986068
SN - 1463-9262
VL - 26
SP - 4723
EP - 4732
JO - Green Chemistry
JF - Green Chemistry
IS - 8
ER -