Unusual Structure-Energy Correlations in Intramolecular Diels–Alder Reaction Transition States [PDF]
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 ...
Justyna M. Żurek +3 more
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Aqueous Ti(IV)-Catalyzed Diels-Alder Reaction
The aqueous Diels-Alder reaction of 1,3-cyclohexadiene with 1,4-benzoquinone was compared and contrasted to the same reaction catalyzed with Flextyl P™, a novel Ti(IV) performance catalyst.
Kyle E. Litz
doaj +2 more sources
Studies of novel diazanaphthoquinones and ion-responsive fluorescent quinoxaline derivatives [PDF]
This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University.The work reported is divided into two parts: fIrstly a section dealing with the preparation of some novel diazanaphthoquinones and their reactions ...
Ahmad, Abid Rafiq
core +7 more sources
Enzymatic intermolecular Diels-Alder reactions in synthesis: From nature to design
The Diels-Alder (D-A) reaction is one of the most critical chemical transformations to construct C–C bonds with predictable regio- and stereo-selectivities. It has been widely used as a retrosynthetic disconnection in synthetic chemistry.
Lei Gao, Jun Yang, Xiaoguang Lei
doaj +1 more source
Machine Learning to Predict Diels-Alder Reaction Barriers from the Reactant State Electron Density [PDF]
Reaction barriers are key to our understanding of chemical reactivity and catalysis. Certain reactions are so seminal in chemistry, that countless variants, with or without catalysts, have been studied and their barriers have been computed
Matthew, Hennefarth +3 more
core +2 more sources
Reversible Diels–Alder Reactions with a Fluorescent Dye on the Surface of Magnetite Nanoparticles
Diels–Alder reactions on the surface of nanoparticles allow a thermoreversible functionalization of the nanosized building blocks. We report the synthesis of well-defined magnetite nanoparticles by thermal decomposition reaction and their ...
Siyang He, Guido Kickelbick
doaj +1 more source
Highly-functionalised difluorinated (hydroxymethyl)conduritol analogues via the Diels-Alder reactions of a difluorinated dienophile [PDF]
A difluorodienophile, synthesised using a Stille coupling reaction underwent tin(IV)-catalysed cycloaddition with three furans to afford oxa[2.2.1]bicycloheptenes in good yield.
Moralee, Andrew C +8 more
core +4 more sources
Salicylaldehyde containing biaryls are efficiently synthesized via an unprecedented amine promoted Diels-Alder-retro-Diels-Alder cascade reaction of ynals with 2-pyrones in good yields.
Xixi Song +5 more
doaj +1 more source
The pentadehydro-Diels–Alder reaction [PDF]
In the classic Diels-Alder [4 + 2] cycloaddition reaction, the overall degree of unsaturation (or oxidation state) of the 4π (diene) and 2π (dienophile) pairs of reactants dictates the oxidation state of the newly formed six-membered carbocycle. For example, in the classic Diels-Alder reaction, butadiene and ethylene combine to produce cyclohexene ...
Wang, Teng +3 more
openaire +2 more sources
Synthesis of the [11]Cyclacene Framework by Repetitive Diels–Alder Cycloadditions
The Diels–Alder cycloaddition between bisdienes and bisdienophile incorporating the 7-oxa-bicyclo[2.2.1]heptane unit are well known to show high diastereoselectivity that can be exploited for the synthesis of molecular belts. The related bisdiene 5,6,7,8-
John B. Bauer +4 more
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