cycloaddition


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cycloaddition

(ˌsaɪkləʊəˈdɪʃən)
n
a type of pericyclic chemical reaction
Translations
cycloaddition
References in periodicals archive ?
Subsequently,1,3-diploar cycloaddition of azomethineylide 4 with acrylates 5 or 1,4-naphthoquinone 6 produces the final products (Scheme 1).
In the second one, It is proposed to explore the virgin territory of n2~s cycloaddition reactivity, Thanks to bimetallic cooperativity.
9-Anthracene carboxylic acid (AC) was photodimerized in solution under UV light via |4 + 4] cycloaddition to form cyclooctane-type rings, with prominently head-to-tail structures [64].
The trigger is a cycloaddition group containing carbamoylnitroso or azo groups and cyclic 1,3-dienes that are covalently coupled to the ends of the polymer chains.
leaf extract and their catalytic activity for the Huisgen [3 + 2] cycloaddition of azides and alkynes at room temperature.
8:30 [3+2] CYCLOADDITION REACTIONS OF ARYL NITRILE OXIDES AND DIENES, Gloria de la Garza *, James C.
A variety of chemical reactions have been utilized to achieve the self-healing process such as those that promote the formation of covalent bonds like the Diels-Alder reactions between furan and maleimide groups [7, 8], cycloaddition reactions [2 + 2] with cinnamoyl derivatives [9], and photochemical cycloaddition reactions [4 + 4] with anthracene derivatives [10].
Scala, "N-Substituted and N-unsubstituted 1,3-Oxazolium-5-olates cycloaddition reactions with 3-substituted coumarins," Tetrahedron, vol.
Chapters are: environmental applications of multifunctional nanocomposite catalytic materials; chemical transformation of molecular precursor into well-defined nanostructural functional framework via soft chemical approach; graphenes in heterogeneous catalysis; gold nanoparticlesugraphene composites material; hydrogen generation from chemical hydrides; ring-opening polymerization of lactide; catalytic performance of metal alkoxides; cycloaddition of Co20 and epoxides over reusable solid catalysts; catalytic metal-/bio-composites for fine chemicals derived from biomass production; homoleptic metal carbonyls in organic transformation; zeolites; optimizing zeolitic catalysis for environmental remediation.
These THQ compounds were prepared using a three-component cationic imino Diels-Alder cycloaddition methodology and a catalytic reduction (Romero & Kouznetsov 2010) that provided the N-benzyl- or N-H-1,2,3,4-tetrahydroquinoline derivatives with high structural diversity.
Flueggedine (33), a highly symmetric [2 + 2] cycloaddition indolizidine alkaloid dimer, was isolated from the twigs and leaves of Flueggea virosa.