Results 41 to 50 of about 8,749 (208)

Investigation of growth stimulating activity of 2-heteryl-[1,2,4]triazolo [1,5-c]quinazolines and products of its nucleophilic degradation

open access: yesZaporožskij Medicinskij Žurnal, 2013
Nucleophilic degradation of 2-heteryl-[1,2,4]triazolo[1,5-c]quinazolines was investigated and the structure of {2-(3-heteryl)-1H-1,2,4-triazol-5-yl]phenyl}ami­nes was unequivocally proved by spectral methods.
A. K. Bilyi   +2 more
doaj   +1 more source

One-Pot Tandem Synthesis of 2-Arylquinazolines by a Multicomponent Cyclization Reaction

open access: yesMolecules, 2013
A series of 2-arylquinazolines have been synthesized in moderate to excellent yields by one-pot tandem reaction of (2-aminophenyl)methanols, aldehydes and ceric ammonium nitrate (CAN).
Xiaodong Xia   +3 more
doaj   +1 more source

Structure Activity Relationship and Molecular Docking of Some Quinazolines Bearing Sulfamerazine Moiety as New 3CLpro, cPLA2, sPLA2 Inhibitors

open access: yesMolecules, 2023
The current work was conducted to synthesize several novel anti-inflammatory quinazolines having sulfamerazine moieties as new 3CLpro, cPLA2, and sPLA2 inhibitors.
Mohammed Abdalla Hussein   +5 more
doaj   +1 more source

3D,2D-QSAR study and docking of novel quinazolines as potential target drugs for osteosarcoma

open access: yesFrontiers in Pharmacology, 2023
Background: Quinazolines are an important class of benzopyrimidine heterocyclic compounds with a promising antitumor activity that can be used for the design and development of osteosarcoma target compounds.Objective: To predict the compound activity of ...
Zheng Lian   +4 more
doaj   +1 more source

QUINAZOLINES. PART I.

open access: yes, 1937
QUINAZOLINES.
TEJENDRA NATH GHOSH
core   +1 more source

Simple and straight forward synthesis of 2,4-disubstituted quinazolines in aqueous medium [PDF]

open access: yes, 2012
Efficient synthesis of diverse quinazolines from readily available starting materials was achieved in aqueous medium via one-pot protocol. A number of 2,4-disubstituted quinazolines were prepared in moderate to good yields under mild and catalyst-free ...
Bandaru, Madhav   +4 more
core   +1 more source

Potential of substituted quinazolines to interact with multiple targets in the treatment of cancer

open access: yes, 2021
The efficacy of quinazoline-based antiglioma agents has been attributed to their effects on microtubule dynamics. The design, synthesis and biological evaluation of quinazolines as potent inhibitors of multiple intracellular targets, including ...
Hamel, Ernest   +6 more
core   +1 more source

Conjugate Addition of Nucleophiles to the Vinyl Function of 2-Chloro-4-vinylpyrimidine Derivatives

open access: yesMolecules, 2010
Conjugate addition reaction of various nucleophiles across the vinyl group of 2-chloro-4-vinylpyrimidine, 2-chloro-4-(1-phenylvinyl)pyrimidine and 2-chloro-4-vinylquinazoline provides the corresponding 2-chloro-4-(2-substituted ethyl)pyrimidines and 2 ...
Lucjan Strekowski   +4 more
doaj   +1 more source

Convenient synthetic approach to 2,4-disubstituted quinazolines

open access: yes, 2007
2,4-Dialkyl or aryl quinazolines have been prepared in three steps starting from easily available anilides. A photochemically induced Fries rearrangement of the anilides gave several ortho-aminoacylbenzene derivatives that were acylated at the NH2. These
Maurizio Taddei   +5 more
core   +1 more source

Advances in Metal-Catalyzed Cross-Coupling Reactions of Halogenated Quinazolinones and Their Quinazoline Derivatives

open access: yesMolecules, 2014
Halogenated quinazolinones and quinazolines are versatile synthetic intermediates for the metal-catalyzed carbon–carbon bond formation reactions such as the Kumada, Stille, Negishi, Sonogashira, Suzuki-Miyaura and Heck cross-coupling reactions or ...
Malose Jack Mphahlele   +1 more
doaj   +1 more source

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