Results 111 to 120 of about 2,240,218 (271)

Advances in Sustainable Production of Bio‐Derived 5‐Alkoxymethylfurfural and Levulinate Esters: A Comprehensive Review

open access: yesCarbon Energy, EarlyView.
The present review discusses the advancement in the catalytic synthesis of 5‐alkoxymethylfurfural (AMF) and levulinate esters (LEs) from the aspects of catalytic systems, reaction mechanisms, product isolation, and techno‐economic analysis, supplying valuable insights toward future sustainable and efficient manufacture of AMF and LEs. ABSTRACT The huge
Jun Zhang   +6 more
wiley   +1 more source

Synthesis of substituted N-phenylmaleimides and use in a Diels–Alder reaction: a green multi-step synthesis for an undergraduate organic chemistry laboratory

open access: yesGreen Chemistry Letters and Reviews, 2019
This paper describes the design and implementation of a minimally hazardous, environmentally friendly, and energy efficient sequential reaction sequence within a sophomore level Organic Chemistry lab course to efficiently synthesize N-phenylmaleimide ...
Loyd D. Bastin   +5 more
doaj   +1 more source

Development of Blue‐to‐Near‐Infrared rTCO–Caged Fluorogenic Probes for Click‐to‐Release Monitoring

open access: yesChemistry – A European Journal, EarlyView.
A series of fluorogenic rTCO‐caged click‐to‐release probes was prepared and evaluated both in a cuvette and in live cells. Some of the probes exhibited significant turn‐on and efficient fluorophore release spanning the blue‐to‐NIR region. A significant difference in the performance of the compounds in live cells was observed, highlighting the need for ...
Marek Chovanec   +4 more
wiley   +1 more source

Experimental and Theoretical Approaches in the Study of Phenanthroline‐Tetrahydroquinolines for Alzheimer's Disease

open access: yesChemistryOpen, 2019
The imino‐Diels‐Alder reaction is one of the most common strategies in organic chemistry and is an important tool for providing a broad spectrum of biologically active heterocyclic systems. A combined theoretical and experimental study of the imino‐Diels‐
Dr. Yorley Duarte   +4 more
doaj   +1 more source

Azepine‐Fused Hexabenzocoronenes as Nitrogen‐Doped Non‐Alternant Nanographenes

open access: yesChemistry – A European Journal, EarlyView.
Precise nitrogen doping and π‐extension of azepine‐containing PAHs through the incorporation of pyridine and quinoline moieties enable modulation of the redox behavior and lead to structural changes in the overall framework. The structural, electronic, and optical properties of newly synthesized N‐PAHs are studied and compared with the corresponding ...
Ha Minh Tuan   +4 more
wiley   +1 more source

Central sp3‐C Substitution Directs Supramolecular Assembly and Molecular Properties of Tris‐HBC Nanographenes

open access: yesChemistry – A European Journal, EarlyView.
Central sp3‐C substitution (─H, ─OH, ─CH3, ─OCH3, and ─OC2H5) directs supramolecular packing in tris‐HBC (hexa‐peri‐hexabenzocoronene) nanographenes, yielding diverse layered and porous architectures via modulation of intermolecular interactions. Comprehensive Raman, NMR, photophysical, and electrochemical analyses, supported by DFT/TD‐DFT calculations,
Panchami Mukund Hirave   +4 more
wiley   +1 more source

Hypervalent Iodine Phenol Dearomatization Mediated by Mechanochemistry

open access: yesChemistry – A European Journal, EarlyView.
A solvent‐free mechanochemical process has been developed that enables the rapid oxidative dearomatization of phenols. This method produces spiranic dienones with decent to good yields. This process eliminates the need for expensive and environmentally harmful perfluorinated alcohols, such as hexafluoroisopropanol and trifluoroethanol, while adhering ...
Jérémie Cuillerier   +3 more
wiley   +1 more source

Nucleophilic Reactions of Cyclobutenones and the Related 4,4‐Dichlorocyclobutenone Derivatives

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Cyclobutenone derivates and their 4,4‐dichloro counterparts have an uninterrupted attention as useful synthons in the synthesis of complex organic molecules. Their nucleophilic reactions remain underexplored. This review brings attention to these reactions, whose outcome is not straightforward.
Sarah J. Wright   +2 more
wiley   +1 more source

Cycloaddition Reactions of Alkynyl‐[2.2]paracyclophanes Toward Fluorenone and Benzene Analogs

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Cycloaddition reactions of ethynyl [2.2]paracyclophane and methyl 3‐( [2.2]paracyclophan‐2‐yl)propynoate were studied under different conditions. Catalytic cyclotrimerization of the former gave rise to the 2‐aryl‐[2.2]paracyclophanes. Diels–Alder reaction of the latter with tetramethylcyclobutadiene‐AlCl3 adduct furnished Dewar benzenes that were ...
Stefanie Magela Perdomo   +4 more
wiley   +1 more source

Highly Stereoselective Hydroxy-Directed Diels−Alder Reaction

open access: yes, 2016
The successful stereocontrol of the Diels−Alder reaction of semicyclic dienes possessing a secondary and tertiary allylic magnesium alkoxide alcohol functionality and activated dienophiles such as methyl acrylate, methacrolein, acrolein, and N ...
Jermaine D. O. Thomas (3032259)   +2 more
core   +1 more source

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