Results 31 to 40 of about 44,314 (270)

Promotion mechanism of hydroxyl groups in catalyzing CO2 cycloaddition

open access: yesJournal of CO2 Utilization
In this study, a series of hydroxy-functionalized quaternary ammonium salt catalysts, i.e., NEt3(HE)Br, NEt2(HE)2Br, NEt1(HE)3Br, and N(HE)4Br, were successfully prepared by quantitatively grafting hydrogen-bond donors (HBDs) as electrophilic sites on ...
Yiming Wang   +5 more
doaj   +1 more source

Unveiling the Chemistry of Higher-Order Cycloaddition Reactions within the Molecular Electron Density Theory

open access: yesChemistry, 2022
The higher-order cycloaddition (HOCA) reaction of tropone with cyclopentadiene (Cp) has been studied within the Molecular Electron Density Theory.
Luis R. Domingo   +2 more
doaj   +1 more source

Unusual Structure-Energy Correlations in Intramolecular Diels–Alder Reaction Transition States

open access: yes, 2014
Detailed analysis of calculated data from an experimental/computational study of intramolecular furan Diels–Alder reactions has led to the unusual discovery that the mean contraction of the newly forming C-C σ-bonds from the transition state to the ...
Robert L. Rae   +14 more
core   +1 more source

[2+2+2] Cycloaddition Reactions of Macrocyclic Systems Catalyzed by Transition Metals. A Review

open access: yesMolecules, 2010
Polyalkyne and enediyne azamacrocycles are prepared from arenesulfonamides and various alkyne and alkene derivatives either under basic or neutral conditions.
Anna Roglans, Anna Pla-Quintana
doaj   +1 more source

Microwave-Assisted Regioselective Synthesis and 2D-NMR Studies of New 1,2,3-Triazole Compounds Derived from Acridone

open access: yesJournal of Chemistry, 2021
A simple and mild protocol towards the synthesis of new 1,2,3-triazole compounds derived from acridone has been developed via regiospecific 1,3-dipolar cycloaddition reaction between 10-(prop-2-yn-1-yl)acridone derivatives and aromatic azides using CuI ...
Mohammed Aarjane   +3 more
doaj   +1 more source

Synthetic studies on the bioactive tetramic acid JBIR-22 using a late stage Diels-Alder reaction

open access: yes, 2015
The authors would like to thank the following for funding: Cancer Research UK (grants C21383/A6950 and C483/A10706)A late stage Diels-Alder reaction is used to prepare a mixture of JBIR-22, a natural product from the Equisetin family of tetramic acids ...
Healy, A. R., Westwood, Nicholas James
core   +1 more source

The Puzzle of the New Type of Intermediate in the Course of [2 + 2] Cycloaddition with the Participation of Conjugated Nitroalkenes: MEDT Computational Study

open access: yesMolecules
The phenomena of regio- and stereoselectivity and the molecular mechanism of the [2 + 2] cycloaddition reaction between (E)-2-arylnitroethenes and the ynamine molecular system were analyzed using wb97xd/6-311 + G(d) (PCM) quantumchemical calculations. It
Radomir Jasiński, Agnieszka Kącka-Zych
doaj   +1 more source

[4 + 2]-Cycloadditions to 1 '-Phenyl-Substituted 3-Vinylindoles with N-Phenylmaleimide: An Access to New [a]Anellated Carbazole Derivatives

open access: yesCHIMIA, 1987
The AlCl3-catalyzed [4 + 2]-cycloaddition of T-phenyl-substituted 3-vinylindoles with N-phenylmaleimide gives rise to new anellated carbazole derivatives with a high endo-preference.
Ludwig Pfeuffer, Ulf Pindur
doaj   +1 more source

Reactivity of (Z)-4-arylidene-5(4H)-oxazolones: [4+2] cycloaddition versus [4+3] cycloaddition/nucleophilic trapping [PDF]

open access: yes, 2002
The use of different aluminum derivatives in the reaction between cyclopentadiene and (Z)-2-phenyl-4-arylidene-5(4H)-oxazolones, and in particular the use of different equivalents of the reagent, allows the modulation of the synthesis of the norbornane ...
Peregrina, J.M. [0000-0003-3778-7065]   +3 more
core   +1 more source

Design of Amine-Modified Zr–Mg Mixed Oxide Aerogel Nanoarchitectonics with Dual Lewis Acidic and Basic Sites for CO2/Propylene Oxide Cycloaddition Reactions

open access: yesNanomaterials, 2022
The utilization of CO2 attracts much research attention because of global warming. The CO2/epoxide cycloaddition reaction is one technique of CO2 utilization. However, homogeneous catalysts with both Lewis acidic and basic and toxic solvents, such as DMF,
Yi-Feng Lin   +4 more
doaj   +1 more source

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