Results 91 to 100 of about 21,297 (236)

Synthesis and antimicrobial activity of some imidazothiazole derivatives of benzofuran

open access: yes, 2017
A series of 6-(1-benzofuran-2-yl)-3-phenyl imidazo[2,1-b][1,3]thiazole (5a–f) and 3,6-bis (1-benzofuran-2-yl)imidazo[2,1-b][1,3]thiazole (6a–d) derivatives are synthesized by the reaction of 1-(1-benzofuran-2-yl)-2-bromoethanones (2a–b) with 4-phenyl-1,3-
Bodke, Yadav D.   +2 more
core   +1 more source

5-Chloro-3-(4-fluorophenylsulfonyl)-2,7-dimethyl-1-benzofuran

open access: yesActa Crystallographica Section E, 2014
In the title compound, C16H12ClFO3S, the dihedral angle between the plane of the benzofuran ring system [r.m.s. deviation = 0.007 (1) Å] and that of the 4-fluorophenyl ring is 76.11 (5)°.
Hong Dae Choi, Uk Lee
doaj   +1 more source

Remarkable Formation of Indene Derivatives Upon Friedel–Crafts Acylation Reactions

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 23, 16 June 2026.
This shows indene derivatives. Under the reaction conditions of a Friedel–Crafts acylation, alkyl benzenes underwent an unprecedented cyclopentannulation furnishing indene derivatives. Alkylbenzene derivatives react with two equivalents of pivaloyl chloride (PivCl) in the presence of aluminum trichloride under formation of indene derivatives with up to
Leah Bantel   +3 more
wiley   +1 more source

2-Methyl-3-phenylsulfonyl-5-propyl-1-benzofuran [PDF]

open access: yes, 2008
The title compound, C18H18O3S, was prepared by the oxidation of 2-methyl-3-phenylsulfanyl-5-propyl-1-benzofuran with 3-chloroperoxybenzoic acid. The phenyl ring makes a dihedral angle of 81.74 (6)° with the plane of the benzofuran fragment ...
Pil Ja Seo   +3 more
core   +1 more source

A Green and Highly Selective Approach to Copper‐Catalyzed Transfer Hydrodeuteration of Alkenes and Alkynes Using D2O

open access: yesChemSusChem, Volume 19, Issue 11, 15 June 2026.
Highly selective deuteration is now possible with a green and more environmentally benign reaction protocol for Cu‐catalyzed transfer hydrodeuteration of alkenes and alkynes. This was applied to the synthesis of precisely deuterated alkanes, including deuterated complex molecules and high enantiopurity isotopomers. Precisely labeled small molecules are
Aniel J. Rivera Arzola   +5 more
wiley   +1 more source

5-Chloro-2-(4-fluorophenyl)-3-phenylsulfinyl-1-benzofuran

open access: yes, 2011
In the title compound, C20H12ClFO2S, the O atom and the phenyl ring of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran fragment; the phenyl ring is almost perpendicular to this plane [82.44 (5)&#176 ...
Pil Ja Seo   +3 more
core   +1 more source

Benzofuranyl Esters: Synthesis, Crystal Structure Determination, Antimicrobial and Antioxidant Activities

open access: yesMolecules, 2015
A series of five new 2‐(1‐benzofuran‐2‐yl)‐2‐oxoethyl 4-(un/substituted)benzoates 4(a–e), with the general formula of C8H5O(C=O)CH2O(C=O)C6H4X, X = H, Cl, CH3, OCH3 or NO2, was synthesized in high purity and good yield under mild conditions.
C. S. Chidan Kumar   +9 more
doaj   +1 more source

Electrophilic Iodination of Heterocyclic Compounds. Recent Advances 2008–2025: Part II

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 22, 9 June 2026.
Electrophilic iodination using molecular iodine and iodide sources represents an efficient approach for accessing valuable iodinated organic compounds. This review highlights recent advances in the iodination of heterocyclic compounds from 2008 to 2025, emphasizing the role of heteroaryl iodides as important synthetic intermediates for biologically ...
Njomza Ajvazi, Stojan Stavber
wiley   +1 more source

Synthesis of Benzofuran Derivatives via a DMAP-Mediated Tandem Cyclization Reaction Involving ortho-Hydroxy α-Aminosulfones

open access: yesMolecules
An efficient cascade cyclization strategy was developed to synthesize aminobenzofuran spiroindanone and spirobarbituric acid derivatives utilizing 2-bromo-1,3-indandione, 5-bromo-1,3-dimethylbarbituric acid, and ortho-hydroxy α-aminosulfones as ...
Rong-Rong Zhu, Xi-Qiang Hou, Da-Ming Du
doaj   +1 more source

Emerging Trends in Organic Photoreactions Utilizing Disulfides

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 21, 4 June 2026.
Disulfides are versatile, nontoxic alternatives to metal photocatalysts. This review explores their role as photoactivated thiyl‐radical precursors and bifunctional catalysts (HAT/electron shuttling) in diverse transformations. Strategies for electronic tuning and development into recyclable heterogeneous materials are highlighted for sustainable ...
Sunil Kumar   +3 more
wiley   +1 more source

Home - About - Disclaimer - Privacy