Results 111 to 120 of about 7,031 (227)

Effect Of Cooking Methods And Conditions On Heterocyclic Amines Content In Satay And Roasted Marinated Chicken [PDF]

open access: yes, 2009
The objectives of this study were to determine the effect of cooking method on HAs concentration of chicken and beef satay and the effect of marinating and different cooking conditions on HAs concentration of roasted chicken.
Mohd Mukhtar, Mohd Safzan
core  

Антивирусное и интерферониндуцирующее действие аминоэтоксидифенилов [PDF]

open access: yes, 2015
Проблематика. Новосинтезованим сполукам 4,4′-біс-(2-R-етокси)біфенілам притаманні як інтеркаляція в ДНК, так і противірусна активність та здатність індукувати інтерферон. Мета дослідження.
Shemendyuk, O. V.   +11 more
core  

2-Phenylthieno[2,3-b]quinoxaline

open access: yesActa Crystallographica Section E Structure Reports Online, 2012
The title compound, C(16)H(10)N(2)S, is almost planar (r.m.s. deviation for all non-H atoms = 0.080 Å). The dihedral angle between the three fused-ring system and the phenyl ring is 9.26 (3)°. The S atom and the opposite C atom of the thio-phene ring are mutually disordered with an occupancy ratio of 0.7706 (19):0.2294 (19).
Youssef Ramli   +4 more
openaire   +3 more sources

Unexpected Reduction of Ethyl 3-Phenylquinoxaline-2- carboxylate 1,4-Di-N-oxide Derivatives by Amines

open access: yesMolecules, 2008
The unexpected tendency of amines and functionalized hydrazines to reduceethyl 3-phenylquinoxaline-2-carboxylate 1,4-di-N-oxide (1) to afford a quinoxaline 1c andmono-oxide quinoxalines 1a and 1b is described. The experimental conditions werestandardized
Antonio Monge   +5 more
doaj   +1 more source

Oxidant-free annulation of α-hydroxy ketones with diamines using aluminum(III) chloride: A supramolecular approach for practical quinoxaline synthesis

open access: yesResults in Chemistry
The conventional reaction of α-hydroxy ketones (acyloins) with arene-1,2-diamines typically requires an oxidant to facilitate a tandem oxidative condensation, resulting in quinoxaline derivatives. In this study, an innovative approach has been introduced
Maryam Farajpour Mojdehi   +5 more
doaj   +1 more source

Связывание катионов триоксадихиноксалина-дииндолизиноциклопентадекафаном и его ациклическим аналогом [PDF]

open access: yes, 2008
Методом циклической вольтамперометрии исследовано связывание ионов Li⁺, Na⁺, K⁺, Cs⁺, Ag⁺, Zn²⁺, Ni²⁺, Co²⁺ (I группа), H⁺, Mg²⁺, Al³⁺, Ga³⁺ (II группа), Ca²⁺, Pb²⁺ (III группа) 2¹,3¹-дифенил-1²,4²-диоксо-7,10,13-триокса-1,4 (3,1)-дихиноксалина-2 (2,3)
Калинин, А. А.   +4 more
core  

Nuovi derivati chinossalinici inibitori della Diidrofolato Reduttasi (DHFR) e della Timidilato Sintetasi (TS) della Leishmania major: risultati preliminari [PDF]

open access: yes, 2004
L’incidenza delle malattie protozoarie imputate al genere Leishmania è aumentata enormemente con la diffusione dell’AIDS. In particolare la forma viscerale della Leishmaniosi sta emergendo come malattia nuova e sempre più frequente.
Carta, Antonio   +5 more
core  

SYNTHESIS, REACTIVITY AND BIOLOGICAL ACTIVITY OF QUINOXALIN-2-ONE DERIVATIVES

open access: yesScientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, 2010
Quinoxalines have a great interest in various fields and particularly in chemistry, biology and pharmacology. It enabled the researchers to develop many methods for their preparations and to seek new fields of application.
El Mokhtar Essassi   +5 more
doaj  

Les ravageurs et maladies du palmier à huile et du cocotier. Protection des pépinières et prépépinières de palmier à huile contre les acariens (Tetranychidae) [PDF]

open access: yes, 1973
L'emploi abusif de traitements chimiques contre les ravageurs des prépépinières et des pépinières risque de détruire l'équilibre biologique et de favoriser la pullulation d'acariens.
De Taffin, Gabriel, Sourou, B.
core  

EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF); Scientific Opinion on Flavouring Group Evaluation 17, Revision 3 (FGE.17Rev3): Pyrazine derivatives from chemical group 24 [PDF]

open access: yes, 2011
Aeschbacher   +90 more
core   +1 more source

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