Results 31 to 40 of about 14,380 (267)

Simplified Kinetics and Colour Formation in Sucrose Solutions Based on A-Dicarbonyl Compounds [PDF]

open access: yes, 2007
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence
Fiedler, Thorsten   +3 more
core   +1 more source

Synthesis of new derivants 11h-indeno[1,2-b] - quinoxaline as perspective inhibitors of JNK (C-Jun n-terminalnal kinase) [PDF]

open access: yes, 2017
Various quinoxalines show biological activity and have such properties as antiviral, antibacterial, antimicrobial, anti-inflammatory, anticancer, antidepressant, vermicidal, and act as inhibitors of kinases [1].
Коврижина, А. Р.
core   +2 more sources

the very different redox behaviour of isoelectronic complexes with [PtCl2] and [AuCl2]+ [PDF]

open access: yes, 2011
The new, potentially ambidentate heterocyclic ligand 2,3-bis(1-methylimidazol-2-yl)quinoxaline (bmiq) was obtained from 2,3-bis(1-methylimidazol-2-yl)glyoxal and 1,2-diaminobenzene.
Bulak, Ece   +6 more
core   +1 more source

Small Band Gap Polymers Synthesized via a Modified Nitration of 4,7-Dibromo-2,1,3-benzothiadiazole [PDF]

open access: yes, 2010
The nitration of 4,7-dibromo-2,1,3-benzothiadiazole was modified by using CF3SO3H and HNO3 as the nitrating agent, and the related yield was improved greatly.
Andersson, Mats R.   +7 more
core   +1 more source

Preparation, structures and preliminary host–guest studies of fluorinated syn-bis-quinoxaline molecular tweezers

open access: yesBeilstein Journal of Organic Chemistry, 2010
A series of polycyclic frameworks with fluorinated syn-facial quinoxaline sidewalls has been prepared as potential molecular tweezers for electron-rich guest compounds.
Markus Etzkorn   +4 more
doaj   +1 more source

Synthesis and Antimicrobial Activity of Some New Quinoxaline Derivatives

open access: yesPharmaceuticals, 2010
2-Chloro-3-methylquinoxaline was selected as a nucleus around which various molecular transformations were performed to obtain new compounds expected to possess optimized antimicrobial activity.
Ram Gopal Singhal   +3 more
doaj   +1 more source

Steroidal quinoxalines

open access: yesJournal of Heterocyclic Chemistry, 1973
AbstractThe treatment of 3β‐hydroxy‐16α‐bromo‐5α‐androstan‐17‐one, 3β‐acetoxy‐16α‐bromo‐5‐androsten‐17‐one and 21‐bromo‐5‐pregnen‐3β‐ol‐20‐one with 4,5‐dimethyl‐o‐phenylenediamine gave substituted quinoxalines.Hydrolysis of 3β‐acetoxy‐5‐androsteno[16,17‐b]‐6′,7′‐dimethylquinoxaline produced the corresponding 3β‐hydroxy compound.
openaire   +3 more sources

Bromination of quinoxaline and derivatives: Effective synthesis of some new brominated quinoxalines

open access: yesTetrahedron, 2017
Abstract The synthesis of brominated quinoxaline derivatives starting from several kinds of quinoxaline by different bromination strategies was studied. First the synthesis of some brominated quinoxalines was accomplished along with the development of an alternative and effective synthesis of some known compounds.
Sefa Uçar   +3 more
openaire   +5 more sources

2-(3-Nitrophenoxy)quinoxaline [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
In the title mol-ecule, C(14)H(9)N(3)O(3), the dihedral angle between the quinoxaline and benzene rings is 77.13 (9)°. The mol-ecule is twisted about the ether-benzene O-C bond, with a C-O-C-C torsion angle of -102.8 (2)°. In the crystal, mol-ecules are linked by C-H⋯O hydrogen bonds, forming layers in the ab plane, with one nitro O atom accepting two ...
Hassan, N.D.   +5 more
openaire   +5 more sources

QuinoxalineTacrine QT78, a Cholinesterase Inhibitor as a Potential Ligand for Alzheimer’s Disease Therapy

open access: yesMolecules, 2019
We report the synthesis and relevant pharmacological properties of the quinoxalinetacrine (QT) hybrid QT78 in a project targeted to identify new non-hepatotoxic tacrine derivatives for Alzheimer’s disease therapy.
Eva Ramos   +11 more
doaj   +1 more source

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