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ChemInform Abstract: Microwave Enhanced Claisen‐Schmidt Condensation: A Green Route to Chalcones.

ChemInform, 2013
AbstractAn Environmentally benign, solvent‐free synthesis of chalcones (III) is developed.
Jayant P. Singh   +5 more
openaire   +1 more source

Bifunctional Nanocrystalline MgO for Chiral Epoxy Ketones via Claisen−Schmidt Condensation−Asymmetric Epoxidation Reactions

Journal of the American Chemical Society, 2004
Design and development of a truly nanobifunctional heterogeneous catalyst for the Claisen-Schmidt condensation (CSC) of benzaldehydes with acetophenones to yield chalcones quantitatively followed by asymmetric epoxidation (AE) to afford chiral epoxy ketones with moderate to good yields and impressive ee's is described.
Boyapati M, Choudary   +4 more
openaire   +2 more sources

Piperidine‐functionalized silica: an efficient and environmentally benign catalyst for Claisen–Schmidt condensation

Applied Organometallic Chemistry, 2014
Piperidine‐functionalized silica as a basic heterogeneous catalyst was synthesized via a simple protocol by condensing silica chloride with piperidine. The catalyst was characterized with various techniques (FT‐IR, solid state NMR, scanning electron microscopy, energy‐dispersive X‐ray, thermogravimetric, elemental, and NH3 and CO2 temperature ...
Kulsum Khan, Zeba N. Siddiqui
openaire   +1 more source

Probing the Rate-Determining Step of the Claisen-Schmidt Condensation by Competition Reactions

Journal of Chemical Education, 2007
Competition experiments are a useful tool for preliminary study of the linear free energy relationship of organic reactions. This article describes a physical organic experiment for upper-level undergraduates to identify the rate-determining step of the Claisen–Schmidt condensation of benzaldehyde and acetophenone by studying the linear free energy ...
Kendrew K. W. Mak   +5 more
openaire   +1 more source

Zeolites as catalysts in organic reactions. Claisen-Schmidt condensation of acetophenone with benzaldehyde

Catalysis Letters, 1990
HY zeolites catalyze the crossed aldol condensation of acetophenone with benzaldehyde, in benzene at 80 °C, to give trans- and cis-chalcones. Together with these expected products, 3,3-diphenylpropiophenone is also produced. In the analogous basic condensation, using phase transfer catalysis, the Michael adduct was not detected, and besides chalcone a ...
M. J. Climent   +3 more
openaire   +1 more source

An Improved Synthesis of ( E )-Cinnamic Acid Derivatives via the Claisen–Schmidt Condensation

Synthetic Communications, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Masanori Hatsuda   +2 more
openaire   +1 more source

Simple and Effective Protocol for Claisen—Schmidt Condensation of Hindered Cyclic Ketones with Aromatic Aldehydes.

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.
Valeriy Vashchenko   +2 more
openaire   +1 more source

Microwave-Assisted Synthesis of Bis-(Hydroxybenzylidene)-Cycloalkanones via Acid Catalyzed Claisen-Schmidt Condensation

Chemistry & Chemical Technology
In the present study, bis-(hydroxybenzylidene)cycloalkanone derivatives were synthesized by Claisen-Schmidt condensation using cycloalkanones and arylaldehydes in the presence of HCl as an acid catalyst. The synthetic reaction was carried out under microwave irradiation.
Eunike Adabella   +4 more
openaire   +1 more source

Stereoselective and Stereospecific Triflate‐Mediated Intramolecular Schmidt Reaction: Ready Access to Alkaloid Skeletons**

Angewandte Chemie - International Edition, 2021
Lars Gnägi, Remo Arnold, Harish Jangra
exaly  

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