Articles with "aryl" as a keyword



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Chemoselectivity issues of the asymmetric interaction between cyclohexanone, β-nitrostyrene, and benzoic acid under 5-aryl prolinate's organocatalysis.

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Published in 2020 at "Chirality"

DOI: 10.1002/chir.23212

Abstract: 4-l-menthyloxycarbonyl 5-aryl prolinates were studied as organocatalysts of a novel three-component reaction of cyclohexanone, benzoic acid, and β-nitrostyrene. The presence of ortho-halogen atom in 5-aryl fragment of the catalyst is favored for driving the formation… read more here.

Keywords: prolinate; cyclohexanone; benzoic acid; aryl prolinate ... See more keywords
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Mild and Efficient Synthesis of Diverse Organo‐AuI‐L Complexes in Green Solvents

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Published in 2020 at "Chemsuschem"

DOI: 10.1002/cssc.201903415

Abstract: Abstract An exceptionally mild and efficient method was developed for the preparation of (hetero)aryl‐AuI‐L complexes using ethanol or water as the reaction medium at room temperature and Ar‐B(triol)K boronates as the transmetalation partner. The reaction… read more here.

Keywords: efficient synthesis; reaction; aryl; mild efficient ... See more keywords
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SYNTHESIS, STRUCTURE, AND ANTIVIRAL PROPERTIES OF NOVEL 2-ADAMANTYL-5-ARYL-2 H -TETRAZOLES

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Published in 2021 at "Chemistry of Heterocyclic Compounds"

DOI: 10.1007/6073

Abstract: The reaction of 5-aryl- NH -tetrazoles with adamantan-1-ol in concentrated sulfuric acid proceeds regioselectively with the formation of the corresponding 2-adamantyl-5-aryl-2 H -tetrazoles. Nitration of these compounds leads to 2-(adamantan-1-yl)-5-(3-nitroaryl)-2 H -tetrazoles. The structures and… read more here.

Keywords: novel adamantyl; adamantyl aryl; spectroscopy; synthesis structure ... See more keywords
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Synthesis of 1-aryl-6-nitro-1H-benzotriazoles by intramolecular cyclization of 1-aryl-3-(2-fluoro-4-nitrophenyl)- and 1-aryl-3-(2,4-dinitrophenyl)triazenes

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Published in 2018 at "Chemistry of Heterocyclic Compounds"

DOI: 10.1007/s10593-018-2356-1

Abstract: Intramolecular heterocyclization of 1-aryl-3-(2-fluoro-4-nitrophenyl)- and 1-aryl-3-(2,4-dinitrophenyl)triazenes gave 1-aryl-6-nitro-1Н-benzotriazoles containing a nitro group in the benzenoid ring. read more here.

Keywords: aryl fluoro; dinitrophenyl triazenes; nitrophenyl aryl; fluoro nitrophenyl ... See more keywords
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Synthesis and biological evaluation of new 2-aryl-4-((4-aryl-1H-1,2,3-triazol-1-yl)methyl)thiazole derivatives

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Published in 2017 at "Research on Chemical Intermediates"

DOI: 10.1007/s11164-017-3164-4

Abstract: A series of 2-aryl-4-((4-aryl-1H-1,2,3-triazol-1-yl)methyl)thiazole derivatives (8a–p) have been synthesized. The structure of the newly synthesized compounds was determined by spectral analysis. The title compounds were screened for their preliminary antitubercular activity against Mycobacterium tuberculosis H37Ra… read more here.

Keywords: aryl aryl; aryl triazol; methyl thiazole; triazol methyl ... See more keywords

Concise synthesis and biological evaluation of 2-Aryl-3-Anilinobenzo[b]thiophene derivatives as potent apoptosis-inducing agents.

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Published in 2021 at "Bioorganic chemistry"

DOI: 10.1016/j.bioorg.2021.104919

Abstract: Many clinically used agents active in cancer chemotherapy exert their activity through the induction of cell death (apoptosis) by targeting microtubules, altering protein function or inhibiting DNA synthesis. The benzo[b]thiophene scaffold holds a pivotal place… read more here.

Keywords: apoptosis; thiophene; methoxybenzo; aryl ... See more keywords
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Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

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Published in 2017 at "European journal of medicinal chemistry"

DOI: 10.1016/j.ejmech.2016.11.031

Abstract: Current study is based on the biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives 1-26, by treating metronidazole with different aryl and hetero-aryl carboxylic acids in the presence of 1,1'-carbonyl diimidazole (CDI) as a… read more here.

Keywords: biology oriented; drug synthesis; synthesis biods; biology ... See more keywords
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Installation of an aryl boronic acid function into the external section of N-aryl-oxazolidinones: Synthesis and antimicrobial evaluation.

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Published in 2020 at "European journal of medicinal chemistry"

DOI: 10.1016/j.ejmech.2020.113002

Abstract: N-aryl-oxazolidinones is a prominent family of antimicrobials used for treating infections caused by clinically prevalent Gram-positive bacteria. Recently, boron-containing compounds have displayed intriguing potential in the antibiotic discovery setting. Herein, we report the unprecedented introduction… read more here.

Keywords: installation aryl; aryl; aryl oxazolidinones; aryl boronic ... See more keywords
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Phosphorescent monometallic and bimetallic two-coordinate Au(I) complexes with N-heterocyclic carbene and aryl ligands

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Published in 2020 at "Inorganica Chimica Acta"

DOI: 10.1016/j.ica.2020.120188

Abstract: Abstract A series of mononuclear and binuclear two coordinate Au(I) complexes consisting of a MAC carbene ligand (1,3-bis(2,6-diisopropylphenyl)-5,5-dimethyl-4-keto-tetrahydropyridylidene) and an aryl ligand, including phenyl, biphenyl, naphthyl and anthryl, are reported. The oxidation potential is controlled… read more here.

Keywords: ligand; coordinate complexes; two coordinate; carbene ... See more keywords
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Cytotoxicity and DNA interaction in a series of aryl terminated iminopyridine Pt(II) complexes.

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Published in 2020 at "Journal of inorganic biochemistry"

DOI: 10.1016/j.jinorgbio.2020.111335

Abstract: A series of iminopyridine complexes of platinum(II), bearing a flexible diethereal, aryl terminated residue, where the size of aryl group is varied from phenyl to 9-anthracenyl, was synthesized. The new complexes are soluble and stable… read more here.

Keywords: aryl terminated; iminopyridine complexes; series; interaction ... See more keywords
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One-pot two-step stannylation/Stille homocoupling of aryl bromides and iodides under solvent-free conditions

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Published in 2018 at "Mendeleev Communications"

DOI: 10.1016/j.mencom.2018.05.032

Abstract: A new highly efficient solvent-free method for aryl bromide (iodide) homocoupling comprising the use of Pd(OAc)2/PCy3 system in the presence of CsF is suitable for substrates bearing functional groups not tolerant to lithium-, magnesium-, zincorganic… read more here.

Keywords: pot two; step stannylation; two step; one pot ... See more keywords