GREEN SWITCHABLE MULTICOMPONENT REACTIONS FOR SUSTAINABLE HETEROCYCLE SYNTHESIS

4th International Symposium On Biotechnology (2026),  [pp. 873-880]
 
AUTHOR(S) / АУТОР(И): Srđan Tufegdžić , Marijana Živković
 
Download Full Pdf   

DOI: https://doi.org/10.46793/SBT26.873T

ABSTRACT / САЖЕТАК:

An enzyme-assisted green approach was developed for Hantzsch and Biginelli multicomponent reactions using benzaldehyde, acetylacetone, and urea in a glycerol–water buffer. Two known compounds were prepared using identical temperature profiles, citrate buffers, MgSO₄, and glycerol as an emulsion stabilizer. Product chemoselectivity was controlled by tuning pH, reagent ratios, MgSO₄ concentration, and the presence or absence of urease. The results demonstrate biotechnology-assisted pathway control in competing multicomponent reactions within a sustainable synthetic framework. Reactions at 65 °C afforded ~40% yields, with fluorescence properties confirming product formation.

KEYWORDS / КЉУЧНЕ РЕЧИ:

green chemistry, heterocyclic chemistry, Biginelli reaction, Hantzsch reaction, urease (Canavalia ensiformis)

ACKNOWLEDGEMENT / ПРОЈЕКАТ:

The research presented in this article was financially supported by the Ministry for Science, Technological Development and Innovation of the Republic of Serbia (Grant no. 451-03-136/2025-03/200026)

REFERENCES / ЛИТЕРАТУРA:

  • Siva S. Panda, Pankaj Khanna and Leena Khanna (2012) Biginelli Reaction: A Green Perspective, Current Organic Chemistry, 16, 507-520
  • Fatemeh Tamaddon, Somayeh Ghazi (2015) Urease: A highly biocompatible catalyst for switchable Biginelli reaction and synthesis of 1,4-dihydropyridines from the in situ formed ammonia. Catalysis Communications, 72, 63-67.
  • Fatemeh Tamaddon, Davood Arab, Ehsan Ahmadi-AhmadAbadi (2020) Urease immobilization on magnetic micro/nano-cellulose dialdehydes: Urease inhibitory of Biginelli product in Hantzsch reaction by urea. Carbohydrate Polymers, 229, 115471-115480.
  • Gan Zhu, Yiqun Li (2021) Urease: a highly efficient biocatalyst for synthesis of polyhydroquinolines and polyhydroacridines from the ammonia formed in situ. Molecular Diversity, 25, 2149-2159.