نتایج جستجو برای: trisubstituted imidazoles

تعداد نتایج: 4534  

2014
Yogesh Kumar Vijay Bahadur Anil Kumar Singh Virinder Singh Parmar Erik V Van der Eycken Brajendra Kumar Singh

A microwave-assisted synthesis of 2-(4-((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-1H-benzo[d]imidazoles from a phenylazide, propargyloxybenzaldehyde and a 1,2-diaminobenzene is proposed.

Journal: :Chemical communications 2015
Jorge S Valera Joaquín Calbo Rafael Gómez Enrique Ortí Luis Sánchez

The supramolecular polymerization of pyrene imidazoles 1 and 2, governed by H-bonding and C-H···π interactions, yields aggregates showing the characteristic bluish emission pattern of pyrene-based monomers.

Journal: :Journal of biochemistry 1998
Y K Li H S Hsu L F Chang G Chen

Series of 4-arylimidazoles, omega-N-acylhistamines and 4-(omega-phenylalkyl)imidazoles were synthesized in order to probe the active site topology of sweet almond beta-glucosidase. These imidazole derivatives were shown to be very powerful competitive inhibitors. Among the 20 tested compounds, omega-N-benzoylhistamine and 4-(3'-phenylpropyl)imidazole are the most potent inhibitors of the enzyme...

Journal: :Chemical communications 2010
Vijay Gopalsamuthiram Rui Huang William D Wulff

A facile synthesis of optically active mono and trisubstituted calix[4]arenes is described wherein the chirality at the methylene bridges arises from centers of chirality present in the diyne and the bis-carbene complex from which they are constructed.

Journal: :Chemical communications 2014
Aditi P Chavannavar Allen G Oliver Brandon L Ashfeld

An umpolung approach toward nitrone construction utilizing a phosphine-mediated addition of 1,2-dicarbonyls to nitroso compounds is reported. The reaction exhibits a high degree of chemoselectivity and provides direct access to isoxazolidines, imines, and trisubstituted alkenes.

Journal: :Chemical communications 2012
Guanyinsheng Qiu Jie Wu

Carbodiimide reacts with isocyanide catalyzed by copper(i) iodide, leading to benzoimidazo[1,5-a]imidazoles in good yields. This reaction is efficient, and proceeds through a formal [3+2] cycloaddition and C-N coupling.

Journal: :Annals of the Rheumatic Diseases 1969

Journal: :Canadian Journal of Chemistry 1982

Journal: :Chemical communications 2011
Anahit Pews-Davtyan Matthias Beller

Starting from commercially available amines and propargylamides a variety of substituted imidazoles were synthesized via a novel hydroamination-cyclization sequence. The target compounds are obtained in good to excellent yields in the presence of catalytic amounts of zinc triflate.

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