Novel Hybrid Heterocycles Based on 1,4-Diphenylpiperazine Moiety: Synthesis via Hantzsch and Biginelli Reactions, Molecular Docking Simulation, and Antimicrobial Activities. [PDF]
Diab HM +7 more
europepmc +1 more source
2-Azidobenzaldehyde-Enabled Construction of Quinazoline Derivatives: A Review. [PDF]
Qiu W, Zhan D, Ma X, Zhang X.
europepmc +1 more source
Multicomponent Green Synthesis Involving Aryl Aldehydes and Trapped Enols: Dimerization over Cyclization. [PDF]
Zingales SK +9 more
europepmc +1 more source
Competitive cyclization of ethyl trifluoroacetoacetate and methyl ketones with 1,3-diamino-2-propanol into hydrogenated oxazolo- and pyrimido-condensed pyridones. [PDF]
Kushch SO +8 more
europepmc +1 more source
A retrospective 9-years overview of sulfated polyborate as a robust catalyst for organic transformations. [PDF]
Chhaperwal P +4 more
europepmc +1 more source
Innovative synthesis of antimicrobial Biginelli compounds using a recyclable iron oxide-based magnetic nanocatalyst. [PDF]
Taravati A +3 more
europepmc +1 more source
The Biginelli Reaction Is a Urea-Catalyzed Organocatalytic Multicomponent Reaction [PDF]
The recently developed artificial force induced reaction (AFIR) method was applied to search systematically all possible multicomponent pathways for the Biginelli reaction mechanism. The most favorable pathway starts with the condensation of the urea and benzaldehyde, followed by the addition of ethyl acetoacetate.
Maneeporn, Puripat +5 more
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Biginelli reaction: an overview
Tetrahedron Letters, 2016Abstract Biginelli reaction involves acid-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) using easily-accessible starting materials, namely, aldehyde, active methylene compound and (thio)urea. DHPMs have stimulated resurgence of interest in the past two decades due to their wide ranging pharmacological activities and presence ...
Arindam Mukhopadhyay +1 more
exaly +2 more sources
The utilization of the Biginelli reaction, a one-pot condensation of an aldehyde, a β-keto ester, and urea, is described. This reaction involves a number of individual steps, each of which is accessible to first-year organic students. The product, a 3,4-dihydropyrimidinone, is a member of a medicinally useful class of compounds.
Michael S. Holden, R. David Crouch
openaire +1 more source

