Results 31 to 40 of about 47,767 (156)

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

Radiation-induced oxidation of substituted benzaldehydes: a pulse radiolysis study

open access: yes, 2004
The reactions of the oxidizing radicals hydroxyl radical (·OH), azidyl radical(N3•) and sulfate radical anion(SO4-•) with hydroxy-, methoxy-, chloro- and nitro-substituted benzaldehydes were studied by pulse radiolysis.
Mohan, H.   +3 more
core   +1 more source

KINETIC STUDIES ON THE ALKYLATING ACTIVITY OF CERTAIN NEW CHALCONES OF ACETYLPYRIDINES [PDF]

open access: yesBulletin of Pharmaceutical Sciences. Assiut University, 1995
The synthesis of a number of chalcones derived from acetylpyridines and some p-substituted benzaldehydes has been accomplished. These compounds were evaluated for their alkylating activity by kinetic studies of their reaction with 2-mercaptoethanol ...
N. El-Koussi
doaj   +1 more source

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

Theoretical Studies on the Fluorescence Enhancement of Benzaldehydes by Intermolecular Hydrogen Bonding

open access: yes, 2019
Density functional theory and its time-dependent extension are employed to investigate the intermolecular hydrogen-bonding- (Inter-HB-) induced fluorescence enhancement of benzaldehydes. The fluorescence quenching mechanism of benzaldehydes in chloroform
Keyao Li (5503166)   +2 more
core   +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

Home - About - Disclaimer - Privacy