Results 31 to 40 of about 51,441 (193)

Degradation of chlorinated benzaldehydes in aqueous solutions by UV-irradiation

open access: yesInternational Journal of Photoenergy, 2002
Photoinduced degradation of chlorinated benzaldehydes was investigated using UV light with λ = 253.7 nm in aerated aqueous solutions. Substrate degradation rate as expressed by first order reaction kinetics revealed rate constants, k; 7.45×10−3 min-1, 3 ...
Miray Bekbölet, Nikola Getoff
doaj   +1 more source

Synthesis and Characterization of Chiral Nitrobenzaldehyde - Schiff Base Ligands

open access: yesMolecules, 2003
Three chiral nitrobenzaldehyde/Schiff base ligands (2a-c) were prepared by the reaction of ortho, meta, and para-NO2 substituted benzaldehydes (1a-c) with (1R,2R)-(-)-1,2-diaminocyclohexane. The structures of ligands 2a-c were characterized by IR, 1H-NMR,
Zhuo Zheng, Wen Tao Gao
doaj   +1 more source

Large acceleration under highly concentrated conditions: Synthesis of chalcones using a small amount of DMF or [emim]N(CN)2

open access: yesResults in Chemistry, 2022
A variety of chalcones were synthesized by the reactions between benzaldehydes and acetophenones catalyzed by Ba(OH)2. The reactions in the presence of a small amount of DMF or 1-ethyl-3-methylimidazolium dicyanamide ([emim]N(CN)2) were faster than those
Kiyoshi Tanemura
doaj   +1 more source

Benzaldehyde-Functionalized Polymer Vesicles [PDF]

open access: yesACS Nano, 2009
Polymer vesicles with diameters of ca. 100-600 nm and bearing benzaldehyde functionalities within the vesicular walls were constructed through self-assembly of an amphiphilic block copolymer PEO(45)-b-PVBA(26) in water. The reactivity of the benzaldehyde functionalities was verified by cross-linking the polymersomes and also by a one-pot cross-linking ...
Guorong, Sun   +7 more
openaire   +2 more sources

Tricarbonyl(h6-Arene)Chromium(0) Complexes as Chiral Auxiliaries: Asymmetric Synthesis of b-Lactones

open access: yesMolecules, 2001
The optically pure tricarbonyl(h6-2-substituted benzaldehydes)chromium are used as chiral auxiliaries in the condensation with a series of doubly lithiated carboxylic acids. The intramolecular ring closure of the obtained Cr(CO)3 complexed b-hydroxyacids
Deborah Montrasio, Paola Del Buttero
doaj   +1 more source

Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reaction

open access: yesBeilstein Journal of Organic Chemistry, 2014
Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolcular [1,5]-hydride shift/isomerization reaction has been realized, using the inherent reducing power of 3-pyrrolines.
Chun-Huan Jiang   +6 more
doaj   +1 more source

Síntese de derivados 4-aril-3,4-di-hidrocumarínicos catalisada por NbCl5

open access: yesQuímica Nova, 2013
Multicomponent reactions between phenols, β-diesters and benzaldehydes for the synthesis of 4-aryl-3,4-dihydrocoumarin derivatives were carried out under mild conditions (room temperature) and presented moderate yields (38-88%) and reasonable reaction ...
Willian Henrique dos Santos   +2 more
doaj   +1 more source

Synthesis of Oxygenated ortho-Methylbenzaldehydes via Aryne [2+2] Cycloaddition and Benzocyclobutenol Ring Opening

open access: yesCHIMIA, 2018
Herein, a two-step procedure for the preparation of oxygenated ortho-methylbenzaldehyde derivatives, starting from commercially available bromoarenes, is described.
Mark M. Maturi   +2 more
doaj   +1 more source

On the application of knoevenagel condensation for the synthesis of benzylidene benzothiazine compounds and structural study

open access: yesQuímica Nova, 2006
The synthesis and physico-chemical properties of new 6-acetylamino or 6-benzoyl-amino 2-benzylidene-4-methyl-4H-benzo[1,4]thiazin-3-ones and 6-benzoylamino or 6-nitro 2-benzylidene-4H-benzo[1,4]thiazin-3-ones are described.
Ana Maria Alves de Souza   +6 more
doaj   +3 more sources

Synthesis and Spectral Characterization of Some New Substituted Bis-spirocyclohexanones Derived from Acetone

open access: yesScience Journal of University of Zakho, 2018
Diarylidene acetones (DAA) (1-5) had been prepared by the condensation of acetone with substituted benzaldehydes via Claisen-Schmidt reaction, DAA’s brought to condense with anthrone to afford the title compounds (6-10) through Michael addition.
Mohammed S. Hussein   +2 more
doaj   +1 more source

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