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Aminoheterocycles as synthons for combinatorial Biginelli reactions
Molecular Diversity, 2010Chlorotrimethylsilane (TMSCl) has been utilized as an efficient promoter and water scavenger in the synthesis of diverse dihydropyrimidines via Biginelli type MCR-heterocyclization using aminoheterocycles. High yields and a simple workup of target compounds enable the facile generation of combinatorial libraries comprising more than 2,000 compounds of ...
Sergey V, Ryabukhin +4 more
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Recent progress in asymmetric Biginelli reaction
Molecular Diversity, 2013The Biginelli reaction, which involves the interaction of ethyl acetoacetate, urea, and an appropriate aryl aldehyde, was first discovered by Pietro Biginelli about 120 years ago. The Biginelli products (3,4-dihydropyrimidin-2(1H)-ones) are interesting materials due to their significant pharmacological and structural profiles.
Majid M, Heravi +2 more
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Tandem Hydroformylation-Biginelli Reaction
Synlett, 2013The combination of a tandem process with a multicomponent reaction is a new approach to high atom-economic synthesis. A tandem hydroformylation–Biginelli reaction sequence has been developed leading to a variety of functionalized 4-alkyl-substituted 3,4-dihydropyrimidin-2(1H)-ones.
Fuchs, Daniela +4 more
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ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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Organosilane sulfonated graphene oxide in the Biginelli and Biginelli-like reactions
New Journal of Chemistry, 2016The acid functionalized SSi-GO was used as a highly active, selective and reusable catalyst to improve the formation of pyrimidinones.
Javad Safari +2 more
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Biginelli Reaction: A Green Perspective
Current Organic Chemistry, 2012The Biginelli Reaction is a one-pot acid catalysed cyclocondensation of -keto ester, urea and aromatic aldehyde which leads to the synthesis of functionalised 3,4-dihydro-2(H)-pyrimidinones (DHPMs). This three-component reaction for the synthesis of dihydro- pyrimidinone and corresponding dihydropyrimidinethiones has now been known for more than a ...
Siva S. Panda +2 more
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The Biginelli Reaction Is a Urea-Catalyzed Organocatalytic Multicomponent Reaction
The Journal of Organic Chemistry, 2015The 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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New catalysts of Biginelli reaction
Russian Journal of Organic Chemistry, 2007A synthesis was developed of new imidazole derivatives catalyzing three-component condensation of ethyl acetoacetate, aromatic aldehydes, and urea(or thiourea) by Biginelli reaction.
F. Makaev +5 more
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2-Acylthioacetamides in the Biginelli Reaction
Chemistry of Heterocyclic Compounds, 2014We have demonstrated for the first time a Biginelli reaction of 2-acylthioacetamides with aromatic aldehydes and ureas or thioureas, leading to N-Ar1-4-Ar2-6-R1-1-R2-2-oxo(thioxo)-1,2,3,4-tetrahydro-pyrimidine-5-carbothioamides. The regioselectivity of this process matched the concept of hard/soft Lewis acids and bases.
M. N. Kurmach +2 more
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ChemInform Abstract: Biginelli Reaction
ChemInform, 2008AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Anil Saini +2 more
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