Results 1 to 10 of about 30,052 (209)

3-Methylsulfinyl-2-phenyl-1-benzofuran [PDF]

open access: yesActa Crystallographica Section E, 2008
The title compound, C15H12O2S, was prepared by the oxidation of 3-methylsulfanyl-2-phenyl-1-benzofuran with 3-chloroperoxybenzoic acid. The phenyl ring makes a dihedral angle of 37.65 (8)° with the plane of the benzofuran fragment.
Uk Lee   +3 more
doaj   +3 more sources

2,4,6-Trimethyl-3-phenylsulfinyl-1-benzofuran [PDF]

open access: yesActa Crystallographica Section E, 2008
The title compound, C17H16O2S, was prepared by the oxidation of 2,4,6-trimethyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the planar ...
Hong Dae Choi   +3 more
doaj   +3 more sources

2-Methyl-3-phenylsulfinyl-1-benzofuran [PDF]

open access: yesActa Crystallographica Section E, 2008
The title compound, C15H12O2S, was prepared by the oxidation of 2-methyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran
Hong Dae Choi   +3 more
doaj   +3 more sources

An Exploration of the Inhibitory Mechanism of Rationally Screened Benzofuran-1,3,4-Oxadiazoles and-1,2,4-Triazoles as Inhibitors of NS5B RdRp Hepatitis C Virus through Pharmacoinformatic Approaches

open access: yesBiomedicines, 2023
Benzofuran, 1,3,4-oxadiazole, and 1,2,4-triazole are privileged heterocyclic moieties that display the most promising and wide spectrum of biological activities against a wide variety of diseases. In the current study, benzofuran-1,3,4-oxadiazole BF1–BF7
Ali Irfan   +9 more
doaj   +1 more source

In Silico Development of Novel Benzofuran-1,3,4-Oxadiazoles as Lead Inhibitors of M. tuberculosis Polyketide Synthase 13

open access: yesPharmaceuticals, 2023
Benzofuran and 1,3,4-oxadiazole are privileged and versatile heterocyclic pharmacophores which display a broad spectrum of biological and pharmacological therapeutic potential against a wide variety of diseases.
Ali Irfan   +10 more
doaj   +1 more source

Synthesis of Elaborate Benzofuran-2-Carboxamide Derivatives through a Combination of 8-Aminoquinoline Directed C–H Arylation and Transamidation Chemistry

open access: yesMolecules, 2020
Herein, we present a short and highly modular synthetic route that involves 8-aminoquinoline directed C−H arylation and transamidation chemistry, and which enables access to a wide range of elaborate benzofuran-2-carboxamides.
Michael Oschmann   +3 more
doaj   +1 more source

Benzofuran as a promising scaffold for the synthesis of antimicrobial and antibreast cancer agents: A review

open access: yesJournal of Research in Medical Sciences, 2015
Benzofuran as an important heterocyclic compound is extensively found in natural products as well as synthetic materials. Since benzofuran drivatives display a diverse array of pharmacological activities, an interest in developing new biologically active
Ghadamali Khodarahmi   +3 more
doaj   +1 more source

A New Pathway for the Synthesis of a New Class of Blue Fluorescent Benzofuran Derivatives

open access: yesMolecules, 2018
In this study an efficient and straightforward method for obtaining a new class of blue fluorescent bezofuran derivatives, under microwave irradiation, as well as under conventional thermal heating, is presented. Under conventional TH the reactions occur
Costel Moldoveanu   +4 more
doaj   +1 more source

Metabolites With Cytotoxic Activities From the Mangrove Endophytic Fungus Fusarium sp. 2ST2

open access: yesFrontiers in Chemistry, 2022
Two new 3-decalinoyltetramic acid derivatives with peroxide bridge fusarisetins E (1) and F (2), one new chromone fusarimone A (5), two new benzofurans fusarifurans A (9) and B (10), three new isocoumarins fusarimarins A–C (11–13), as well as five known ...
Yan Chen   +8 more
doaj   +1 more source

5-Iodo-2,7-dimethyl-3-phenylsulfinyl-1-benzofuran

open access: yesActa Crystallographica Section E, 2008
The title compound, C16H13IO2S, was prepared by the oxidation of 5-iodo-2,7-dimethyl-3-phenylsulfanyl-1-benzofuran using 3-chloroperbenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the ...
Uk Lee   +3 more
doaj   +1 more source

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