89185-49-9

Upstream product

• 89185-43-3 (4-Methoxy-phenyl)-[(Z)-pyrimidin-2-ylimino]-acetonitrile 
• 30469-01-3 2-(4-methoxy-phenyl)-3-nitroso-imidazo[1,2-a]pyrimidine 
• 109-12-6 2-aminopyrimidine 
• 7677-24-9 trimethylsilyl cyanide 
• 123-11-5 4-methoxy-benzaldehyde 
• 31555-35-8 2-(p-methoxyphenyl)imidazo[1,2-a]pyrimidine 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Relevant academic research and scientific papers

Ultrasonic assisted synthesis of imidazo[1,2-a]azine catalyzed by ZnO nanorods

ZnO nanorods have been successfully used as an efficient, economic, and reusable catalyst for the synthesis of imidazo[1,2-a]azine under ultrasonic irradiation. This procedure offers advantages in terms of higher yields, short reaction times and mild reac

Ionic liquid promoted one-pot three-component reaction: Synthesis of annulated imidazo[1,2-a]azines using trimethylsilylcyanide

Imidazo[1,2-a]azine derivatives are synthesized by a one-pot three-component reaction of an 2-aminoazine, an aldehyde, and trimethylsilylcyanide in the presence of 1-n-butyl-3-methylimidazolium bromide as a recoverable ionic liquid, in moderate to excelle

ZnO nanorods as an efficient catalyst for the synthesis of imidazo[1,2-a]azines and diazines

ZnO nanorods were synthesized using a novel and solvent-free procedure and their catalytic activity in the preparation of imidazo[1,2-a]azines and diazines was studied. The effects of the amount of catalyst and its reusability were investigated to optimiz

Synthesis and antibacterial activity of some imidazo[1,2-a[pyrimidine derivatives

A series of 75 imidazo[1,2-a]pyrimidine derivatives were synthesized. The 'in vitro' antibacterial activity of these compounds and their corresponding α-bromoketones against a variety of gram (+), gram (-) bacteria and Mycobacterium species is reported. Some of the prepared derivatives exhibited potent antimicrobial activity.

Cyclisation Reactions of some 3-Nitrosoimidazo-pyridines and -pyrimidines. Ring-opening/Ring-closure Reactions with Triethyl Phosphite: Reassignment by X-Ray Crystal Structure and Nuclear Magnetic Resonance

Deoxygenation of 3-nitroso-2-phenylimidazo-pyridines and -pyrimidines with triethyl phosphite does not lead to the products described in the literature as pyrido- and pyrimido-imidazoindoles (3) and (4), but to the open-chain derivatives, N-(2-pyri